SlideShare ist ein Scribd-Unternehmen logo
1 von 101
Cancer of the Anal Canal
U.S. GI Intergroup
 Compared mitomycin vs cisplatin
 The rate of colostomy at 5 years was
significantly lower in the mitomycin, 5-FU,
radiation arm (10 vs. 19%; P = .04).
 Disease-free and overall survival rates were
similar in each group.
 Grade 3-4 hematologic toxicity was higher in
those who received mitomycin (60% vs.
42%) but other acute toxicity levels were
similar.
 The combination of 5-FU, mitomycin, and
radiation was recommended as the
preferred standard of care.
The combination of radiation, 5-
FU, and mitomycin
5-year survival rates local control rates
 80% for (T1)
 70% for (T2)
 45% to 55% for larger or
deeply invasive cancers
(T3 or T4)
 65% to 75% overall
 90% to 100% - (T1)
 65% to 75% - (T2)
 40% to 55% - (T3 or
T4)
 60% overall.
 Up to 5% of patients
overall lost anorectal
function because of
treatment-related
morbidity
Timing of delivery of
chemotherapy
 The importance of timing relative to
radiation each day is not known.
 Mainly by analogy with the results of
trials already completed in more
common cancers, and by general
usage, the delivery of 96- to 120-hour
infusions of 5-FU, together with bolus
injections of cisplatin or mitomycin on
the first or second day of the 5-FU
infusion, is the schedule used most
widely.
Increasing the total radiation dose and
shortening the overall duration of the radiation
schedules
 When combined with 5-FU and mitomycin –
- 30 Gy in 3 weeks eradicate up to about
90% ( < 3 cm in size).
- Higher doses, from 45 Gy in 5 weeks to 54
Gy in 6 weeks, sometimes supplemented by
additional radiation after an interval of 6 to 8
weeks - controlled 65% to 75% larger than
4 cm.70
 Improved tumor control was observed .
 Although the patients also received higher
total doses of chemotherapy, increase in
radiation dose was the more significant
factor.
INTRODUCTION
 Cancer of the anal canal is an uncommon malignancy,
accounting for approximately 1.5% to 2% of all cancers
of the lower alimentary tract in the United States.
 The risk of anal canal cancer has increased over the past
30 years with its association with HPV and HIV.
ANATOMY
 The anal canal is a 4-cm-long structure that passes downward and
backward from the rectal ampulla (level of pelvic floor) to the anus (anal
verge).
 The proximal border of the anal canal clinically corresponds to the anal
sphincter at the level of the puborectalis muscle (palpable as the anorectal
ring on digital rectal examination). This is where the rectum enters the
puborectalis sling, made by fibers from both sides.
 The distal end of the anal canal is at the level of the anal verge, where the
groove between the internal sphincter and the subcutaneous part of the
external sphincter is palpable.
 This also is the level of the squamous-mucocutaneous junction and the
perianal skin.
 It follows that two distinct categories of tumors arise in
the anal region.
 Tumors that develop from mucosa (columnar,
transitional, or squamous) are true anal canal cancers
tumors
 that arise from skin at or distal to the squamous-
mucocutaneous junction are termed anal margin
tumors
definitions
 Anal Canal= 4 cm mucosa
lined region from junction of the
puborectalis portion of the
levator ani muscle and the
external anal sphincter, and
extends distally to the anal
verge
 Transitional zone- from
glandular (columnar) to
squamous mucosa- at dentate
line
 Anal Margin- begins at the
anal verge. It represents the
transition from the squamous
mucosa to the epidermis-lined
perianal skin.
Rectal
glandular
mucosa
Transitional
Squamous
True Epidermis
epidemiology
 Relatively uncommon.
 Seen in middle age- median age at
diagnosis 61 years.
 Slight female preponderance
 Incidence is increasing possibly due to
association with hpv.
 More common in men having anal
receptive intercourse and hiv +.
ETIOLOGY AND RISK
FACTORS
 HPV infection
 Immunosuppression- transplant
patients and those with HIV.
 Cigarrete smoking- 5 FOLD increased
risk
 Benign anal conditions -- fistulae,
fissures, and hemorrhoids -- do not
appear to predispose to cancer .
 Fissures may facilitate the access of
high-risk HPV to basal epithelial cell
layers.
 Any increased risk of cancer from
chronic IBD -
? Discontinued ( danish population
based study )
AIN
 Presence of cellular and nuclear
abnormalities in the perianal and anal
epithelium without a breach of the
epithelial basement membrane.
 Precursor to scc of anal canal.
 Parallel observations in the cervix in
which HPV infection causes the
development of CIN, the precursor lesion
to invasive cervical cancer.
AIN = squamous intraepithelial lesion
(SIL)
Also called carcinoma in situ and
Bowen’s dz
AIN 1 = LSIL
AIN 2&3 = HSIL
AIN & HIV
 Limited data for HIV negatve pts
AIN 1 (LSIL)
- LSIL progresses to HSIL in more than 50
percent of HIV-positive homosexual males
within two years.
AIN 2&3 (HSIL)
- risk for progression to invasive cancer
ranges from 10 to 50 percent among HIV
positive patients
Among HPV-infected individuals, the
prevalence of HSIL and anal carcinoma is
higher in those with concomitant HIV infection
compared to those who are HIV-negative.
HPV and AIN
 HPV causes anal intraepithelial
neoplasia(AIN) which progresses from
low grade to high grade dysplasia and
ultimately to invasive cancer.
 Hpv 16 & 18 are strongly implicated.
 As anal lesions progress there is also
accumulation of mutant p53
expressions.
 The high-risk HPV E6 and E7 proteins
are thought to contribute to the
induction of anogenital cancers by
interacting with and degrading the
function of p53 and pRb, respectively.
 HPV DNA integration is needed for
transition from low- to high-grade AIN.
 Loss of heterozygosity at 11q23 is the
most consistent event, and appears to
be independent of human
immunodeficiency virus (HIV) status.
 Anal pap smears – sensitiivity 69 to
93% and specificity ranges from 32 to
59%.
 Anoscopy, anal cytology, and high-
resolution anal colposcopy each play
a role in the assessment of AIN.
 High-grade AIN recurs or persists after
treatment in less than 25% of those
who are HIV-negative, but in up to
80% of HIV-positive patients.
Management of AIN
 Excision is for clinically definable lesions.
WLE guided by frozen sections.
1 cm margins
Large defects closed with local flaps
WLE is associated with high rates of disease recurrence
and anal incontinence/stenosis
 Targeted destruction guided by high-resolution anoscopy
Decreased morbidity compared to WLE
High risk for persistent or recurrent disease among HIV+
Surveillance examinations performed at six-month
intervals as long as dysplasia is present
 Treatment with imiquimod or 5-fluorouracil has initial 50-
90% response rates.
Recurrence limited with long duration therapy
Compliance limited by significant skin irritation
 Photodynamic therapy.
 Some authors recommend
observation only for wide-field low
grade AIN, and even for high-grade
AIN when there are no signs of
invasive cancer, if the risk of functional
damage due to ablative treatment is
considered too great.
WHO Classification of Anal
Cancer
Anal canal
 Squamous cell carcinoma
- Keratinizing (below dentate)
- Nonkeratinizing (above dentate)
- Basaloid (transitional)
 Adenocarcinoma
- Rectal type
- Of anal glands
- Within anorectal fistula
 Small cell carcinoma
 Undifferentiated
“Anal Cancer” = squamous cell
cancer arising in the mucosa of
the anal canal
Anal margin
 Squamous cell carcinoma
 Giant condyloma
 Basal cell carcinoma
 Others (Melanoma)
 Bowen's disease (SCC in situ)
 Paget's disease (Intraepithelial
adenocarcinoma)
Classification of tumor is
determined by the
pathology/histology of the
tumor not the anatomic
location as determined by the
surgeon or endoscopist.
NATURAL HISTORY
 Anal cancer is predominantly a locoregional disease, with possible
direct extension to surrounding tissues and lymphatic dissemination
to inguinal and pelvic nodes; hematogenous distant metastasis is a
relatively rarer occurrence.
 Anal canal cancers constitute 75% of all lesions, and only 25% are
anal margin tumors.
 Local spread may be present in approximately 50% of cancers at
diagnosis with involvement of the anal sphincter or surrounding soft
tissues.
 Extension to the rectum and perianal skin also may occur.
 Invasion of the vaginal septum is more common than invasion of
the prostate gland because of the presence of Denonvillier’s fascia
in men, which acts as a barrier
 Lymphatic drainage is dependent on the anatomic location of the primary
tumor.
 Tumors that arise distal to the dentate line drain to inguinal lymph nodes
(superficial and deep), and those above the dentate line spread primarily to
the internal iliac system, and with more proximal lesions, spread occurs to
the inferior mesenteric group.
 The regional nodes are considered to be inguinal (superficial and deep
femoral), internal iliac, and perirectal (anorectal, perirectal, and lateral
sacral). All other nodal groups represent sites of distant disease.
 The incidence of involvement of inguinal nodes is directly proportional to
the size and extent of the primary tumor. Overall, this risk may be
approximately 10% at diagnosis but may increase to 20% for tumors larger
than 4 cm, and with T4 disease, this may be as high as 60%.
 Distant metastasis may occur to any organ, but the liver and
lungs are most frequently involved. Overall, distant
metastases are relatively rare.
 At diagnosis, only 5% to 10% of patients will be found to
have distant disease.
 After curative treatment, the risk of distant disease varies,
ranging between 10% and 30%, and depends on the initial
tumor (T) stage.
 The risk of distant metastasis also increases with the number
of regional nodes involved
CLINICAL PRESENTATION
AND DIAGNOSIS
 Most patients with anal cancer are first seen with rectal bleeding.
This occurs in approximately 50% of patients;
 30% experience pain or the sensation of a rectal mass.
 Pruritus in 30%
 Altered bowel habbits -rare
 A common concern with most anal neoplasms is the frequent delay
in diagnosis resulting from confusion with more common, benign
conditions. Thus, the clinician must maintain a high index of
suspicion when evaluating lesions of the anal canal and margin.
 An interval of 4 to 6 months may ensue between onset of symptoms
and diagnosis in up to 50% of patients.
WORK UP
 Physical examination
1. Regional lymph nodes
2. Adjacent organs for direct invasion
3. Anogenital areas for concurrent malignancies
 Proctoscopy &Biopsy of primary tumor
 Fine-needle aspiration biopsy or simple excision of enlarged
inguinal nodes
 Chest radiograph
 CT/MRI of abdomen and pelvis( mri preferrd as delineates soft
tissue planes better and also better to detect involvement of urethra
or vagina)
 HIV antibody assay, if risk factors are present
 EUS to evaluate for sphincter
involvement and perianal lymph
nodes.
 Consider PET scan since 25% of
patients have metastatic disease by
PET not seen on CT and 20% of
inguinal nodes negative by CT are
PET positive.
STAGING
 PRIMARY TUMOR (T)
 TX Primary tumor cannot be assessed
 T0 No evidence of primary tumor
 Tis Carcinoma in situ
 T1 Tumor =2 cm in greatest dimension
 T2 Tumor >2 cm but =5 cm in greatest dimension
 T3 Tumor >5 cm in greatest dimension
 T4 Tumor of any size invades adjacent organ(s) (e.g., vagina,
urethra, bladder)
 Direct invasion of the rectal wall, perirectal skin, subcutaneous
tissue, or the sphincter muscle(s) is not classified as T4
 REGIONAL LYMPH NODES (N)
 NX Regional lymph nodes cannot be assessed
 N0 No regional lymph node metastasis
 N1 Metastasis in perirectal lymph node(s)
 N2 Metastasis in unilateral internal iliac and/or inguinal lymph
node(s)
 N3 Metastasis in perirectal and inguinal lymph nodes and/or
bilateral internal iliac and/or inguinal lymph node
AJCC stage groups
 Stage I T1 N0 M0
 Stage II T2 N0 M0
T3 N0 M0
 Stage IIIA T1 N1 M0
T2 N1 M0
T3 N1 M0
T4 N0 M0
 Stage IIIB T4 N1 M0
Any T N3 M0
Any T N2 M0
 Stage IV Any T Any N M1
PROGNOSIS
 5 y survival-
T1 — 86 percent
T2 — 86 percent
T3 — 60 percent
T4 — 45 percent
N0 — 76 percent
N+ — 54 percent
Molecular prognostic factors
 High expression of p53 associated
with decreased DFS.
 Also local control rates are lower with
increased p53 expression.
 High level of Ki 67 – longer DFS.
SURGICAL
MANAGEMENT
Surgery
 Surgical treatment was the primary therapy 20 to 35 years ago, but
it has been replaced by sphincter-sparing therapy with combination
chemoradiotherapy.
 Surgical therapy is now used most often as a method of salvage.
 Surgical treatment, when it was used as a primary therapy, required
an abdominoperineal resection (APR).
 This consisted of wide local excision of the anus, to include the
levator ani muscles and contents of the ischiorectal fossa.
 The operation results in a permanent colostomy, as well as loss of
sexual function, in most patients.
 Overall, 5-year survival rates were approximately 50-70% in
different serieses.
Radical resection
 For intermediate-stage primary anal canal
cancer who -
- Cannot tolerate radiation therapy or
chemoradiation
- Incontinent because of irreversible damage of
the sphincters
- Anovaginal fistula
- Prior pelvic radiation treatment (most
frequently for carcinoma of the cervix)
- Active inflammatory bowel disease affecting
the rectum or anal region
- Failure of chemoradiation or radiation and less
frequently, complications of the initial treatment.
Residual cancer
 Suspected residual cancer should be confirmed
by biopsy.
 Random biopsies from the site of the primary
cancer in the absence of clinical features .
 Residual masses after radiation or
chemoradiation may take several months to
regress fully.
 Frequent examination by an experienced
observer is desirable, including, if necessary,
examination under anesthesia.
 C/F - hard-edged ulcer
- an enlarging mass
- increasing pain
SALVAGE SURGERY
 Locoregional failure in 30%
½ recurrence, ½ progression
Salvage APR is associated with five-
year survival rates from 24 to 58%
 Salvage Surge
APR = abdominoperineal resection
Pelvic exenteration = multiviseral
resection
 Urinary and fecal diversion
RECURRENCES
 Strictly, all local recurrences are due to
residual cancer.
 Salvage surgery offers a potential for
long-term local control and survival in
roughly one third to one half of the
patients fit for surgery who do not have
clearly unresectable cancer or known
extrapelvic disease.
 Need reconstructive surgery to close
defects in irradiated pelvic tissues should
be considered.
Prognostic variables
 Node positivity
 Size of the resected tumor
 Status of resection margins
 An analysis of the pathologic data from
patients in the UKCCCR trial showed –
lateral excision margin free of
cancer
> 1 mm - recurrence occurred in
25%
< 1mm - recurrence occurred in
Problems in Surgery
 Perineal wound healing  skin
breakdown
 fistula
formation,
 Malnutrition
 Debility due to pain
 Flap reconstruction should be
considered
TREATMENT OF
LYMPHATICS
 Lymphatic Drainage
Lymphatic drainage of anal cancers
depends on the location of the tumor in
relation to the dentate line.
Tumors below the dentate line drain to
the inguinal and femoral nodes.
Tumors above the dentate line drain to
the perirectal and paravertebral nodes, a
pattern similar to that seen with rectal
cancers.
Tumors in the most proximal portion of
the canal drain to the nodes of the inferior
mesenteric system.
Lymph Node Management
 Chemoradiation is the treatment of choice for inguinal lymph
node disease
Cure rates approach 90 percent for synchronous disease
Bilateral groins should be incorporated into the radiation
fields with the addition of a boost for clinically positive lymph
nodes.
Metachronous lymph nodes + in 10 to 20%
Usually appearing w/in six months after treatment
Respond well to CRT
 Formal node dissection is reserved for metastases residual
or recurrent after radiation-based treatment.
CLINICALLY NORMAL NODES
 If dissected - significant postoperative wound healing
problems or chronic lymphedema.
 Rate of late failure in clinically normal inguinal nodes not
treated prophylactically ranges from about 10% to 25%.
 May prove uncontrollable in up to one half of the patients.
 Because of the morbidity - elective lymphadenectomy of
clinically normal inguinal nodes is not recommended.
 Elective irradiation of clinically normal inguinal node areas
- little morbidity
- reduces the risk of late node failure in the volume
irradiated to less than 5%
Sentinel Lymph Node Bx
 SLNB identifies inguinal metastases in
10–40% of anal cancer patients with
limited morbidity ranging between 3%
and 7%.
The clinical impact of this procedure
on the therapeutic approach is
unclear as long as the inguinal nodes
are included in the radiation field.
APR
The Technique
Pre-operative
 Consent
 Bowel preparation
 Stomal therapy and siting for
stoma
 DVT prophylaxis
 Antibiotics
 Urinary catheter
The Technique
Set-up
 Extended Lloyd-Davies position
 Good assistance
 Long midline incision
 Wide retraction
 Small bowel packed out of the way
 Full laparotomy (liver etc)
Operative Position
TME
Principle is that the sharp
dissection(diathermy/ scissors) should
only proceed in the areolar tissue
plane(holy plane) within and thus
sparing the autonomic nerve plexuses,
the non visceral presacral fat pad, the
parietal sidewall fascia of the pelvis, the
hypogastric plexus, vesicles and
prostate in males and vagina in
females.
 The sigmoid is grasped with toothed
forceps and reflected medially The
adjacent adhesive bands are divided
with long curves scissors, and the
peritoneal reflection is retracted
laterally with forceps. Following this
procedure, the sigmoid is usually
mobilized easily toward the midline.
The peritoneal surface on the left
side of the colon is picked up with
forceps and divided with long,
curved, blunt-nosed Metzenbaum
scissors, which are gently
introduced downward beneath the
peritoneum to separate the
underlying structures, such as the
left spermatic, or ovarian, vessels or
ureter, from the peritoneum to avoid
their accidental injury. The
peritoneum is incised down to the
cul-de-sac on the left side
APR
 The inferior mesenteric vein is often
divided above the left colic branch and
a mobilization of the splenic flexure is
performed so as to allow creation of
the descending colostomy without
tension. The blood supply to the
descending colon is now derived from
the middle colic artery via the marginal
artery of Drummond.
Ligation Inferior Mesenteric Vein
 Although involved lymph nodes may not be
evident in the mesentery over the bifurcation
of the aorta, it is desirable to ligate the inferior
mesenteric artery just distal to the origin of
the left colic artery . The contents of the
proximal clamps are tied, and the ligation is
reinforced by a transfixing suture.
 Some prefer to ligate the inferior mesenteric
artery as near its point of origin from the aorta
as possible. Usually, this level is near the
ligament of Treitz. The blood supply to the
sigmoid to be used as a colostomy is now
derived from the middle artery through the
marginal artery of Drummond.
High Ligation Inferior
Mesenteric Artery
 The peritoneum
along the right side
of the rectosigmoid
junction is incised
lateral to the
inferior mesenteric
and superior
hemorrhoidal
vessels .
 This incision extends down to the
pouch of Douglas. The right ureter is
identified beneath the residual
peritoneum, and its course over the
iliac vessels is exposed with blunt
gauze dissection. The proximal
bowel is retracted anteriorly and
laterally. The superior hypogastric
nerves are visualized just below the
iliac vessels and the ureters. The
dissection proceeds behind the
superior hemorrhoidal vessels
toward the entrance of the presacral
space behind the sacral promontory.
Division of the retrosacral fascia or
ligament just below the sacral
curvature at about S2 is done
sharply in the midline with scissors
or electrocautery.
 The peritoneal reflection in
the pouch of Douglas is
incised about 1 cm up its
anterior reflection over the
bladder in men (shown in
this illustration) or behind
the uterus in women. The
bladder or uterus is
retracted anteriorly using a
fiberoptic lighted deep
pelvic retractor. The sharp
dissection proceeds
anterior to Denonvilliers'
fascia until the prostate and
seminal vessels or the
rectovaginal septum is
seen.
 The paths of the
anterior and
posterior
dissections (Figure
9) show the close
adherence to the
presacral fascia
posteriorly and to
the actual prostate
and seminal
vesicles anteriorly.
 The two lateral dissections in the TME are time-
consuming, as the surgeon carefully proceeds to
expose the parietal fascia over the lateral pelvic wall
structures.
 The fiberoptic lighted deep pelvic retractors are
essential for clear visualization during lateral retraction
of the rectum and anterior elevation of the bladder or
the uterus and vagina.
 The preservation of the pelvic autonomic nerve plexus
and the anterior roots of sacral nerves S2, S3, and S4
is essential for anal continence and sexual function. The
plexus is seen as a dense plaque of nerve tissue that
comes close to the rectum at the level of the prostate or
upper vagina
 . The TME does not encounter "lateral
suspensory ligaments" but rather a fusion of
the lateral mesorectum with tissue that may
contain the middle hemorrhoidal arteries as
the dissection heads toward the autonomic
nerve plexus.
 This tissue is divided with electrocautery, and
the middle hemorrhoidal vessels may require
a ligature. The course of the ureters and the
autonomic plexus is noted as the dissection
is carried down to the levators
The Technique
Preparation Proximal Bowel
The Technique
Preparation Proximal Bowel
The Technique
Preparation Proximal Bowel
PERINEAL PART
 The skin in the
region of the anal
orifice is seized
with several Allis
forceps, and the
incision is made
through the skin
and subcutaneous
tissue at least 2 cm
away from the
closed anal orifice
 All blood vessels
are clamped and
tied to prevent
further loss of
blood as the
operation
progresses
 he posterior portion of
the incision is extended
backward over the
coccyx, and the anus is
tipped upward to enable
its attachments to the
coccyx to be severed
more readily. After the
anococcygeal raphe is
severed and the
presacral space is
entered, the
accumulated blood from
above is suctioned out.
 The levator muscle is
exposed on one side
and, with the finger held
beneath it, is divided
between paired clamps
as far from the rectum
as possible.Following
the ligation of all
bleeding points on one
side, a similar division of
the levator ani muscles
is carried out on the
opposite side.
Alternatively, the levator
muscles may be
transected with
electrocautery.
 Palpation of the inlying
urethral catheter will
facilitate the procedure by
localizing the urethra and
preventing accidental injury
to the prostate, urethra.
The skin and subcutaneous
tissue of the perineum are
retracted upward, while the
anus is pulled downward
and backward to assist in
the exposure. The rectum
is pulled down, the
remaining attachments of
the levator ani muscles and
transversus perinea are
divided, and all bleeding
points are ligated
 . In the female the
dissection between the
rectum and vagina is
more easily
accomplished if
counterresistance is
applied to the posterior
vaginal wall by the
surgeon's fingers. In the
presence of extensive
infiltrating growths it may
be necessary to excise
the perineal body as well
as a portion of the
posterior vaginal wall.
Resected Specimen
Abdominoperineal resection
Anal Margin Cancers
 Anal margin -distal end of the anal canal to a 5-
cm margin surrounding the verge.
 Treat similar to skin cancer.
 WLE for T1 and early T2 lesions that can be
excised with a 1-cm margin.
 Larger T2 cancers -add prophylactic radiation to
the inguinal lymph nodes along with radiation or
excision of the primary tumor.
 T3 and T4 lesions- radiation to both inguinal
regions and the pelvis, along with 5-FU and
mitomycin C.
 APR for bulky tumors extending into the
sphincter or surrounding structures.
 When possible, initial surgical
management is preferred to radiation-
based treatment of perianal cancers
because of the frequent morbidity from
long-term changes in the perianal skin
after irradiation.
 The regional nodes for the perianal skin are the
inguinal nodes.
 Perirectal or pelvic node metastases are very
uncommon.
 The risk of inguinal node metastases is about
10%, associated mainly with category T3 or T4
tumors, or poorly differentiated cancers.
 Elective inguinal nodal irradiation has been
suggested for those categories only.
 The management of abnormal inguinal nodes is
similar to that of anal canal cancer.
THANK YOU….

Weitere ähnliche Inhalte

Was ist angesagt?

BCT - AIIMS Experience
BCT - AIIMS ExperienceBCT - AIIMS Experience
BCT - AIIMS Experienceguest8887a7
 
esophageal cancer surgery types and complications
esophageal cancer surgery types and complicationsesophageal cancer surgery types and complications
esophageal cancer surgery types and complicationsved sah
 
Cancer of vulva
Cancer of vulvaCancer of vulva
Cancer of vulvadrmcbansal
 
Transanal total mesorectal excision
Transanal total mesorectal excisionTransanal total mesorectal excision
Transanal total mesorectal excisionAbhishek Thakur
 
Malignant tumours of thyroid
Malignant tumours of thyroidMalignant tumours of thyroid
Malignant tumours of thyroidkanwalpreet15
 
Staging and Diagnostic approach of rectal cancer
 Staging and Diagnostic approach  of rectal cancer Staging and Diagnostic approach  of rectal cancer
Staging and Diagnostic approach of rectal cancerDr.Bhavin Vadodariya
 
Metastatic liver disease (2)
Metastatic liver disease (2)Metastatic liver disease (2)
Metastatic liver disease (2)mostafa hegazy
 
Malignant pleural effusions
Malignant pleural effusionsMalignant pleural effusions
Malignant pleural effusionsKamal Bharathi
 
LOCALLY ADVANCED BREAST CANCER
LOCALLY ADVANCED BREAST CANCERLOCALLY ADVANCED BREAST CANCER
LOCALLY ADVANCED BREAST CANCERDrAyush Garg
 
Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...
Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...
Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...Dr.Bhavin Vadodariya
 
Colorectal carcinoma anatomy to management
Colorectal carcinoma  anatomy to managementColorectal carcinoma  anatomy to management
Colorectal carcinoma anatomy to managementDrAyush Garg
 
Satyajeet Carcinoma Stomach management
Satyajeet Carcinoma Stomach management Satyajeet Carcinoma Stomach management
Satyajeet Carcinoma Stomach management Satyajeet Rath
 
RECTUM CANCER MANAGEMENT
RECTUM CANCER MANAGEMENTRECTUM CANCER MANAGEMENT
RECTUM CANCER MANAGEMENTKanhu Charan
 
Border line ovarian Tumor
Border line ovarian Tumor Border line ovarian Tumor
Border line ovarian Tumor awad abdou
 
Role of chemotherapy in carcinoma stomach
Role of chemotherapy in carcinoma stomachRole of chemotherapy in carcinoma stomach
Role of chemotherapy in carcinoma stomachSailendra Parida
 

Was ist angesagt? (20)

BCT - AIIMS Experience
BCT - AIIMS ExperienceBCT - AIIMS Experience
BCT - AIIMS Experience
 
esophageal cancer surgery types and complications
esophageal cancer surgery types and complicationsesophageal cancer surgery types and complications
esophageal cancer surgery types and complications
 
Cancer of vulva
Cancer of vulvaCancer of vulva
Cancer of vulva
 
Transanal total mesorectal excision
Transanal total mesorectal excisionTransanal total mesorectal excision
Transanal total mesorectal excision
 
Anal Cancer
Anal CancerAnal Cancer
Anal Cancer
 
Breast carcinoma
Breast carcinoma Breast carcinoma
Breast carcinoma
 
Malignant tumours of thyroid
Malignant tumours of thyroidMalignant tumours of thyroid
Malignant tumours of thyroid
 
Staging and Diagnostic approach of rectal cancer
 Staging and Diagnostic approach  of rectal cancer Staging and Diagnostic approach  of rectal cancer
Staging and Diagnostic approach of rectal cancer
 
Metastatic liver disease (2)
Metastatic liver disease (2)Metastatic liver disease (2)
Metastatic liver disease (2)
 
Malignant pleural effusions
Malignant pleural effusionsMalignant pleural effusions
Malignant pleural effusions
 
LOCALLY ADVANCED BREAST CANCER
LOCALLY ADVANCED BREAST CANCERLOCALLY ADVANCED BREAST CANCER
LOCALLY ADVANCED BREAST CANCER
 
Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...
Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...
Landmark trials in breast Cancer surgery - NSABP 04,06,MILAN,EORTC 10853, ECO...
 
Colorectal carcinoma anatomy to management
Colorectal carcinoma  anatomy to managementColorectal carcinoma  anatomy to management
Colorectal carcinoma anatomy to management
 
Satyajeet Carcinoma Stomach management
Satyajeet Carcinoma Stomach management Satyajeet Carcinoma Stomach management
Satyajeet Carcinoma Stomach management
 
RECTUM CANCER MANAGEMENT
RECTUM CANCER MANAGEMENTRECTUM CANCER MANAGEMENT
RECTUM CANCER MANAGEMENT
 
Anal Malignancy
Anal MalignancyAnal Malignancy
Anal Malignancy
 
Ca anal canal
Ca anal canalCa anal canal
Ca anal canal
 
Border line ovarian Tumor
Border line ovarian Tumor Border line ovarian Tumor
Border line ovarian Tumor
 
Role of chemotherapy in carcinoma stomach
Role of chemotherapy in carcinoma stomachRole of chemotherapy in carcinoma stomach
Role of chemotherapy in carcinoma stomach
 
testicular tumors
testicular tumorstesticular tumors
testicular tumors
 

Ähnlich wie cancer of anal canal

Cancer of the anal canal
Cancer of the anal canalCancer of the anal canal
Cancer of the anal canalNilesh Kucha
 
Vulvar and vaginal cancer epidemiology and molecular pathogenesis
Vulvar and vaginal cancer epidemiology and molecular pathogenesisVulvar and vaginal cancer epidemiology and molecular pathogenesis
Vulvar and vaginal cancer epidemiology and molecular pathogenesisSravanthi Nuthalapati
 
Carcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology resident
Carcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology residentCarcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology resident
Carcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology residentDr. Naina Kumar Agarwal
 
Vulval Cancer Diagnosis and Staging
Vulval Cancer Diagnosis and StagingVulval Cancer Diagnosis and Staging
Vulval Cancer Diagnosis and StagingDr.Bhavin Vadodariya
 
ANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAUswatunAortatikaKhas
 
ETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptx
ETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptxETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptx
ETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptxDebashis Routray
 
Management of anal canal tumors with emphasis on treatment(1)
Management of  anal canal tumors with emphasis on treatment(1)Management of  anal canal tumors with emphasis on treatment(1)
Management of anal canal tumors with emphasis on treatment(1)SabaMajid5
 
Etiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervixEtiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervixNiranjan Chavan
 
Etiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervixEtiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervixNiranjan Chavan
 
Hpv virus infections and oropharynx cancer
Hpv virus infections and oropharynx cancerHpv virus infections and oropharynx cancer
Hpv virus infections and oropharynx cancerRobert J Miller MD
 
ca cervix.ppt.pptx cancer cancer of female
ca cervix.ppt.pptx cancer cancer of femaleca cervix.ppt.pptx cancer cancer of female
ca cervix.ppt.pptx cancer cancer of femaleswatisheth8
 
Carcinoma anal canal.pptx
Carcinoma anal canal.pptxCarcinoma anal canal.pptx
Carcinoma anal canal.pptxPradeep Pande
 
Colo-rectal Carcinoma at a glance !!!
Colo-rectal Carcinoma at  a glance !!!Colo-rectal Carcinoma at  a glance !!!
Colo-rectal Carcinoma at a glance !!!Suman Baral
 

Ähnlich wie cancer of anal canal (20)

Cancer of the anal canal
Cancer of the anal canalCancer of the anal canal
Cancer of the anal canal
 
Vulvar and vaginal cancer epidemiology and molecular pathogenesis
Vulvar and vaginal cancer epidemiology and molecular pathogenesisVulvar and vaginal cancer epidemiology and molecular pathogenesis
Vulvar and vaginal cancer epidemiology and molecular pathogenesis
 
Carcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology resident
Carcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology residentCarcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology resident
Carcinoma anal canal - Dr Naina kumar agarwal MCh surgical oncology resident
 
Vulval Cancer Diagnosis and Staging
Vulval Cancer Diagnosis and StagingVulval Cancer Diagnosis and Staging
Vulval Cancer Diagnosis and Staging
 
ANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
ANAL CARCINOMAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
 
Oral cancer
Oral cancerOral cancer
Oral cancer
 
Carcinoma vagina dr.kiran
Carcinoma vagina  dr.kiranCarcinoma vagina  dr.kiran
Carcinoma vagina dr.kiran
 
ETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptx
ETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptxETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptx
ETIOPATHOGENESIS AND STAGING OF CA PENIS (1).pptx
 
Anal canal
Anal canal Anal canal
Anal canal
 
Management of anal canal tumors with emphasis on treatment(1)
Management of  anal canal tumors with emphasis on treatment(1)Management of  anal canal tumors with emphasis on treatment(1)
Management of anal canal tumors with emphasis on treatment(1)
 
Anal cancer video
Anal cancer videoAnal cancer video
Anal cancer video
 
Etiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervixEtiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervix
 
Etiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervixEtiopathogenesis and natural history of ca cervix
Etiopathogenesis and natural history of ca cervix
 
Hpv virus infections and oropharynx cancer
Hpv virus infections and oropharynx cancerHpv virus infections and oropharynx cancer
Hpv virus infections and oropharynx cancer
 
CARCINOMA PENIS
CARCINOMA PENISCARCINOMA PENIS
CARCINOMA PENIS
 
Cervical Cancer ppt (1).pptx
Cervical Cancer ppt (1).pptxCervical Cancer ppt (1).pptx
Cervical Cancer ppt (1).pptx
 
ca cervix.ppt.pptx cancer cancer of female
ca cervix.ppt.pptx cancer cancer of femaleca cervix.ppt.pptx cancer cancer of female
ca cervix.ppt.pptx cancer cancer of female
 
Ovarian cancer
Ovarian cancerOvarian cancer
Ovarian cancer
 
Carcinoma anal canal.pptx
Carcinoma anal canal.pptxCarcinoma anal canal.pptx
Carcinoma anal canal.pptx
 
Colo-rectal Carcinoma at a glance !!!
Colo-rectal Carcinoma at  a glance !!!Colo-rectal Carcinoma at  a glance !!!
Colo-rectal Carcinoma at a glance !!!
 

Mehr von Nilesh Kucha

Chapter 39 role of radiotherapy in benign diseases.pptx [read only]
Chapter 39 role of radiotherapy in benign diseases.pptx [read only]Chapter 39 role of radiotherapy in benign diseases.pptx [read only]
Chapter 39 role of radiotherapy in benign diseases.pptx [read only]Nilesh Kucha
 
Chapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseasesChapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseasesNilesh Kucha
 
Chapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseasesChapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseasesNilesh Kucha
 
Chapter 38 role of surgery in cancer prevention
Chapter 38 role of surgery in cancer preventionChapter 38 role of surgery in cancer prevention
Chapter 38 role of surgery in cancer preventionNilesh Kucha
 
Chapter 36 t reg cells
Chapter 36 t reg cellsChapter 36 t reg cells
Chapter 36 t reg cellsNilesh Kucha
 
Chapter 35 tumor lysis syndrome
Chapter 35 tumor lysis syndromeChapter 35 tumor lysis syndrome
Chapter 35 tumor lysis syndromeNilesh Kucha
 
Chapter 34 medical stat
Chapter 34 medical statChapter 34 medical stat
Chapter 34 medical statNilesh Kucha
 
Chapter 33 isolated tumor cells
Chapter 33 isolated tumor cellsChapter 33 isolated tumor cells
Chapter 33 isolated tumor cellsNilesh Kucha
 
Chapter 32 invasion and metastasis
Chapter 32 invasion and metastasisChapter 32 invasion and metastasis
Chapter 32 invasion and metastasisNilesh Kucha
 
Chapter 31 genetic counselling
Chapter 31 genetic counsellingChapter 31 genetic counselling
Chapter 31 genetic counsellingNilesh Kucha
 
Chapter 30 febrile neutropenia
Chapter 30 febrile neutropeniaChapter 30 febrile neutropenia
Chapter 30 febrile neutropeniaNilesh Kucha
 
Chapter 29 dendritic cells
Chapter 29 dendritic cellsChapter 29 dendritic cells
Chapter 29 dendritic cellsNilesh Kucha
 
Chapter 28 clincal trials
Chapter 28 clincal trials Chapter 28 clincal trials
Chapter 28 clincal trials Nilesh Kucha
 
Chapter 27 chemotherapy side effects dr lms
Chapter 27 chemotherapy side effects  dr lmsChapter 27 chemotherapy side effects  dr lms
Chapter 27 chemotherapy side effects dr lmsNilesh Kucha
 
Chapter 26 chemoprevention of cancer
Chapter 26 chemoprevention of cancerChapter 26 chemoprevention of cancer
Chapter 26 chemoprevention of cancerNilesh Kucha
 
Chapter 25 assessment of clincal responses
Chapter 25 assessment of clincal responsesChapter 25 assessment of clincal responses
Chapter 25 assessment of clincal responsesNilesh Kucha
 
Chapter 24.3 metronomic chemotherapy
Chapter 24.3 metronomic chemotherapyChapter 24.3 metronomic chemotherapy
Chapter 24.3 metronomic chemotherapyNilesh Kucha
 
Chapter 24.2 lmwh in cancer asso thrombosis
Chapter 24.2 lmwh in cancer asso thrombosisChapter 24.2 lmwh in cancer asso thrombosis
Chapter 24.2 lmwh in cancer asso thrombosisNilesh Kucha
 
Chapter 24.1 kinase inhibitors and monoclonal antibodies
Chapter 24.1 kinase inhibitors and monoclonal antibodiesChapter 24.1 kinase inhibitors and monoclonal antibodies
Chapter 24.1 kinase inhibitors and monoclonal antibodiesNilesh Kucha
 

Mehr von Nilesh Kucha (20)

Chapter 39 role of radiotherapy in benign diseases.pptx [read only]
Chapter 39 role of radiotherapy in benign diseases.pptx [read only]Chapter 39 role of radiotherapy in benign diseases.pptx [read only]
Chapter 39 role of radiotherapy in benign diseases.pptx [read only]
 
Chapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseasesChapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseases
 
Chapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseasesChapter 39 role of radiotherapy in benign diseases
Chapter 39 role of radiotherapy in benign diseases
 
Chapter 38 role of surgery in cancer prevention
Chapter 38 role of surgery in cancer preventionChapter 38 role of surgery in cancer prevention
Chapter 38 role of surgery in cancer prevention
 
Chapter 37 svco
Chapter 37 svcoChapter 37 svco
Chapter 37 svco
 
Chapter 36 t reg cells
Chapter 36 t reg cellsChapter 36 t reg cells
Chapter 36 t reg cells
 
Chapter 35 tumor lysis syndrome
Chapter 35 tumor lysis syndromeChapter 35 tumor lysis syndrome
Chapter 35 tumor lysis syndrome
 
Chapter 34 medical stat
Chapter 34 medical statChapter 34 medical stat
Chapter 34 medical stat
 
Chapter 33 isolated tumor cells
Chapter 33 isolated tumor cellsChapter 33 isolated tumor cells
Chapter 33 isolated tumor cells
 
Chapter 32 invasion and metastasis
Chapter 32 invasion and metastasisChapter 32 invasion and metastasis
Chapter 32 invasion and metastasis
 
Chapter 31 genetic counselling
Chapter 31 genetic counsellingChapter 31 genetic counselling
Chapter 31 genetic counselling
 
Chapter 30 febrile neutropenia
Chapter 30 febrile neutropeniaChapter 30 febrile neutropenia
Chapter 30 febrile neutropenia
 
Chapter 29 dendritic cells
Chapter 29 dendritic cellsChapter 29 dendritic cells
Chapter 29 dendritic cells
 
Chapter 28 clincal trials
Chapter 28 clincal trials Chapter 28 clincal trials
Chapter 28 clincal trials
 
Chapter 27 chemotherapy side effects dr lms
Chapter 27 chemotherapy side effects  dr lmsChapter 27 chemotherapy side effects  dr lms
Chapter 27 chemotherapy side effects dr lms
 
Chapter 26 chemoprevention of cancer
Chapter 26 chemoprevention of cancerChapter 26 chemoprevention of cancer
Chapter 26 chemoprevention of cancer
 
Chapter 25 assessment of clincal responses
Chapter 25 assessment of clincal responsesChapter 25 assessment of clincal responses
Chapter 25 assessment of clincal responses
 
Chapter 24.3 metronomic chemotherapy
Chapter 24.3 metronomic chemotherapyChapter 24.3 metronomic chemotherapy
Chapter 24.3 metronomic chemotherapy
 
Chapter 24.2 lmwh in cancer asso thrombosis
Chapter 24.2 lmwh in cancer asso thrombosisChapter 24.2 lmwh in cancer asso thrombosis
Chapter 24.2 lmwh in cancer asso thrombosis
 
Chapter 24.1 kinase inhibitors and monoclonal antibodies
Chapter 24.1 kinase inhibitors and monoclonal antibodiesChapter 24.1 kinase inhibitors and monoclonal antibodies
Chapter 24.1 kinase inhibitors and monoclonal antibodies
 

Kürzlich hochgeladen

Call Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls Jaipur
Call Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls JaipurCall Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls Jaipur
Call Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls Jaipurparulsinha
 
Call Girls Kochi Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Kochi Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Kochi Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Kochi Just Call 9907093804 Top Class Call Girl Service AvailableDipal Arora
 
Lucknow Call girls - 8800925952 - 24x7 service with hotel room
Lucknow Call girls - 8800925952 - 24x7 service with hotel roomLucknow Call girls - 8800925952 - 24x7 service with hotel room
Lucknow Call girls - 8800925952 - 24x7 service with hotel roomdiscovermytutordmt
 
VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...
VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...
VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...jageshsingh5554
 
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service CoimbatoreCall Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatorenarwatsonia7
 
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...narwatsonia7
 
Vip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls Available
Vip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls AvailableVip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls Available
Vip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls AvailableNehru place Escorts
 
Call Girls Ooty Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ooty Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Ooty Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ooty Just Call 9907093804 Top Class Call Girl Service AvailableDipal Arora
 
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...narwatsonia7
 
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...indiancallgirl4rent
 
Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...
Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...
Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...Call Girls in Nagpur High Profile
 
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoybabeytanya
 
VIP Call Girls Indore Kirti 💚😋 9256729539 🚀 Indore Escorts
VIP Call Girls Indore Kirti 💚😋  9256729539 🚀 Indore EscortsVIP Call Girls Indore Kirti 💚😋  9256729539 🚀 Indore Escorts
VIP Call Girls Indore Kirti 💚😋 9256729539 🚀 Indore Escortsaditipandeya
 
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...narwatsonia7
 
VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...
VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...
VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...Neha Kaur
 
Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...
Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...
Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...narwatsonia7
 
Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...
Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...
Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...Dipal Arora
 
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...CALL GIRLS
 
(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...
(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...
(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...Taniya Sharma
 

Kürzlich hochgeladen (20)

Call Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls Jaipur
Call Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls JaipurCall Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls Jaipur
Call Girls Service Jaipur Grishma WhatsApp ❤8445551418 VIP Call Girls Jaipur
 
Call Girls Kochi Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Kochi Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Kochi Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Kochi Just Call 9907093804 Top Class Call Girl Service Available
 
Lucknow Call girls - 8800925952 - 24x7 service with hotel room
Lucknow Call girls - 8800925952 - 24x7 service with hotel roomLucknow Call girls - 8800925952 - 24x7 service with hotel room
Lucknow Call girls - 8800925952 - 24x7 service with hotel room
 
VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...
VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...
VIP Service Call Girls Sindhi Colony 📳 7877925207 For 18+ VIP Call Girl At Th...
 
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service CoimbatoreCall Girl Coimbatore Prisha☎️  8250192130 Independent Escort Service Coimbatore
Call Girl Coimbatore Prisha☎️ 8250192130 Independent Escort Service Coimbatore
 
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
Top Rated Bangalore Call Girls Mg Road ⟟ 8250192130 ⟟ Call Me For Genuine Sex...
 
Vip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls Available
Vip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls AvailableVip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls Available
Vip Call Girls Anna Salai Chennai 👉 8250192130 ❣️💯 Top Class Girls Available
 
Call Girls Ooty Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ooty Just Call 9907093804 Top Class Call Girl Service AvailableCall Girls Ooty Just Call 9907093804 Top Class Call Girl Service Available
Call Girls Ooty Just Call 9907093804 Top Class Call Girl Service Available
 
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...High Profile Call Girls Coimbatore Saanvi☎️  8250192130 Independent Escort Se...
High Profile Call Girls Coimbatore Saanvi☎️ 8250192130 Independent Escort Se...
 
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
(Rocky) Jaipur Call Girl - 9521753030 Escorts Service 50% Off with Cash ON De...
 
Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...
Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...
Book Paid Powai Call Girls Mumbai 𖠋 9930245274 𖠋Low Budget Full Independent H...
 
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night EnjoyCall Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
Call Girl Number in Panvel Mumbai📲 9833363713 💞 Full Night Enjoy
 
VIP Call Girls Indore Kirti 💚😋 9256729539 🚀 Indore Escorts
VIP Call Girls Indore Kirti 💚😋  9256729539 🚀 Indore EscortsVIP Call Girls Indore Kirti 💚😋  9256729539 🚀 Indore Escorts
VIP Call Girls Indore Kirti 💚😋 9256729539 🚀 Indore Escorts
 
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCREscort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
Escort Service Call Girls In Sarita Vihar,, 99530°56974 Delhi NCR
 
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
VIP Call Girls Tirunelveli Aaradhya 8250192130 Independent Escort Service Tir...
 
VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...
VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...
VIP Russian Call Girls in Varanasi Samaira 8250192130 Independent Escort Serv...
 
Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...
Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...
Top Rated Bangalore Call Girls Richmond Circle ⟟ 8250192130 ⟟ Call Me For Gen...
 
Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...
Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...
Call Girls Bhubaneswar Just Call 9907093804 Top Class Call Girl Service Avail...
 
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
Call Girls Service Surat Samaira ❤️🍑 8250192130 👄 Independent Escort Service ...
 
(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...
(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...
(👑VVIP ISHAAN ) Russian Call Girls Service Navi Mumbai🖕9920874524🖕Independent...
 

cancer of anal canal

  • 1. Cancer of the Anal Canal
  • 2. U.S. GI Intergroup  Compared mitomycin vs cisplatin  The rate of colostomy at 5 years was significantly lower in the mitomycin, 5-FU, radiation arm (10 vs. 19%; P = .04).  Disease-free and overall survival rates were similar in each group.  Grade 3-4 hematologic toxicity was higher in those who received mitomycin (60% vs. 42%) but other acute toxicity levels were similar.  The combination of 5-FU, mitomycin, and radiation was recommended as the preferred standard of care.
  • 3. The combination of radiation, 5- FU, and mitomycin 5-year survival rates local control rates  80% for (T1)  70% for (T2)  45% to 55% for larger or deeply invasive cancers (T3 or T4)  65% to 75% overall  90% to 100% - (T1)  65% to 75% - (T2)  40% to 55% - (T3 or T4)  60% overall.  Up to 5% of patients overall lost anorectal function because of treatment-related morbidity
  • 4. Timing of delivery of chemotherapy  The importance of timing relative to radiation each day is not known.  Mainly by analogy with the results of trials already completed in more common cancers, and by general usage, the delivery of 96- to 120-hour infusions of 5-FU, together with bolus injections of cisplatin or mitomycin on the first or second day of the 5-FU infusion, is the schedule used most widely.
  • 5. Increasing the total radiation dose and shortening the overall duration of the radiation schedules  When combined with 5-FU and mitomycin – - 30 Gy in 3 weeks eradicate up to about 90% ( < 3 cm in size). - Higher doses, from 45 Gy in 5 weeks to 54 Gy in 6 weeks, sometimes supplemented by additional radiation after an interval of 6 to 8 weeks - controlled 65% to 75% larger than 4 cm.70  Improved tumor control was observed .  Although the patients also received higher total doses of chemotherapy, increase in radiation dose was the more significant factor.
  • 6. INTRODUCTION  Cancer of the anal canal is an uncommon malignancy, accounting for approximately 1.5% to 2% of all cancers of the lower alimentary tract in the United States.  The risk of anal canal cancer has increased over the past 30 years with its association with HPV and HIV.
  • 7. ANATOMY  The anal canal is a 4-cm-long structure that passes downward and backward from the rectal ampulla (level of pelvic floor) to the anus (anal verge).  The proximal border of the anal canal clinically corresponds to the anal sphincter at the level of the puborectalis muscle (palpable as the anorectal ring on digital rectal examination). This is where the rectum enters the puborectalis sling, made by fibers from both sides.  The distal end of the anal canal is at the level of the anal verge, where the groove between the internal sphincter and the subcutaneous part of the external sphincter is palpable.  This also is the level of the squamous-mucocutaneous junction and the perianal skin.
  • 8.
  • 9.  It follows that two distinct categories of tumors arise in the anal region.  Tumors that develop from mucosa (columnar, transitional, or squamous) are true anal canal cancers tumors  that arise from skin at or distal to the squamous- mucocutaneous junction are termed anal margin tumors
  • 10.
  • 11. definitions  Anal Canal= 4 cm mucosa lined region from junction of the puborectalis portion of the levator ani muscle and the external anal sphincter, and extends distally to the anal verge  Transitional zone- from glandular (columnar) to squamous mucosa- at dentate line  Anal Margin- begins at the anal verge. It represents the transition from the squamous mucosa to the epidermis-lined perianal skin. Rectal glandular mucosa Transitional Squamous True Epidermis
  • 12. epidemiology  Relatively uncommon.  Seen in middle age- median age at diagnosis 61 years.  Slight female preponderance  Incidence is increasing possibly due to association with hpv.  More common in men having anal receptive intercourse and hiv +.
  • 13. ETIOLOGY AND RISK FACTORS  HPV infection  Immunosuppression- transplant patients and those with HIV.  Cigarrete smoking- 5 FOLD increased risk
  • 14.  Benign anal conditions -- fistulae, fissures, and hemorrhoids -- do not appear to predispose to cancer .  Fissures may facilitate the access of high-risk HPV to basal epithelial cell layers.  Any increased risk of cancer from chronic IBD - ? Discontinued ( danish population based study )
  • 15. AIN  Presence of cellular and nuclear abnormalities in the perianal and anal epithelium without a breach of the epithelial basement membrane.  Precursor to scc of anal canal.
  • 16.  Parallel observations in the cervix in which HPV infection causes the development of CIN, the precursor lesion to invasive cervical cancer. AIN = squamous intraepithelial lesion (SIL) Also called carcinoma in situ and Bowen’s dz AIN 1 = LSIL AIN 2&3 = HSIL
  • 17. AIN & HIV  Limited data for HIV negatve pts AIN 1 (LSIL) - LSIL progresses to HSIL in more than 50 percent of HIV-positive homosexual males within two years. AIN 2&3 (HSIL) - risk for progression to invasive cancer ranges from 10 to 50 percent among HIV positive patients Among HPV-infected individuals, the prevalence of HSIL and anal carcinoma is higher in those with concomitant HIV infection compared to those who are HIV-negative.
  • 18. HPV and AIN  HPV causes anal intraepithelial neoplasia(AIN) which progresses from low grade to high grade dysplasia and ultimately to invasive cancer.  Hpv 16 & 18 are strongly implicated.  As anal lesions progress there is also accumulation of mutant p53 expressions.
  • 19.  The high-risk HPV E6 and E7 proteins are thought to contribute to the induction of anogenital cancers by interacting with and degrading the function of p53 and pRb, respectively.  HPV DNA integration is needed for transition from low- to high-grade AIN.  Loss of heterozygosity at 11q23 is the most consistent event, and appears to be independent of human immunodeficiency virus (HIV) status.
  • 20.  Anal pap smears – sensitiivity 69 to 93% and specificity ranges from 32 to 59%.  Anoscopy, anal cytology, and high- resolution anal colposcopy each play a role in the assessment of AIN.  High-grade AIN recurs or persists after treatment in less than 25% of those who are HIV-negative, but in up to 80% of HIV-positive patients.
  • 21. Management of AIN  Excision is for clinically definable lesions. WLE guided by frozen sections. 1 cm margins Large defects closed with local flaps WLE is associated with high rates of disease recurrence and anal incontinence/stenosis  Targeted destruction guided by high-resolution anoscopy Decreased morbidity compared to WLE High risk for persistent or recurrent disease among HIV+ Surveillance examinations performed at six-month intervals as long as dysplasia is present  Treatment with imiquimod or 5-fluorouracil has initial 50- 90% response rates. Recurrence limited with long duration therapy Compliance limited by significant skin irritation
  • 22.  Photodynamic therapy.  Some authors recommend observation only for wide-field low grade AIN, and even for high-grade AIN when there are no signs of invasive cancer, if the risk of functional damage due to ablative treatment is considered too great.
  • 23. WHO Classification of Anal Cancer Anal canal  Squamous cell carcinoma - Keratinizing (below dentate) - Nonkeratinizing (above dentate) - Basaloid (transitional)  Adenocarcinoma - Rectal type - Of anal glands - Within anorectal fistula  Small cell carcinoma  Undifferentiated “Anal Cancer” = squamous cell cancer arising in the mucosa of the anal canal Anal margin  Squamous cell carcinoma  Giant condyloma  Basal cell carcinoma  Others (Melanoma)  Bowen's disease (SCC in situ)  Paget's disease (Intraepithelial adenocarcinoma) Classification of tumor is determined by the pathology/histology of the tumor not the anatomic location as determined by the surgeon or endoscopist.
  • 24. NATURAL HISTORY  Anal cancer is predominantly a locoregional disease, with possible direct extension to surrounding tissues and lymphatic dissemination to inguinal and pelvic nodes; hematogenous distant metastasis is a relatively rarer occurrence.  Anal canal cancers constitute 75% of all lesions, and only 25% are anal margin tumors.  Local spread may be present in approximately 50% of cancers at diagnosis with involvement of the anal sphincter or surrounding soft tissues.  Extension to the rectum and perianal skin also may occur.  Invasion of the vaginal septum is more common than invasion of the prostate gland because of the presence of Denonvillier’s fascia in men, which acts as a barrier
  • 25.  Lymphatic drainage is dependent on the anatomic location of the primary tumor.  Tumors that arise distal to the dentate line drain to inguinal lymph nodes (superficial and deep), and those above the dentate line spread primarily to the internal iliac system, and with more proximal lesions, spread occurs to the inferior mesenteric group.  The regional nodes are considered to be inguinal (superficial and deep femoral), internal iliac, and perirectal (anorectal, perirectal, and lateral sacral). All other nodal groups represent sites of distant disease.  The incidence of involvement of inguinal nodes is directly proportional to the size and extent of the primary tumor. Overall, this risk may be approximately 10% at diagnosis but may increase to 20% for tumors larger than 4 cm, and with T4 disease, this may be as high as 60%.
  • 26.  Distant metastasis may occur to any organ, but the liver and lungs are most frequently involved. Overall, distant metastases are relatively rare.  At diagnosis, only 5% to 10% of patients will be found to have distant disease.  After curative treatment, the risk of distant disease varies, ranging between 10% and 30%, and depends on the initial tumor (T) stage.  The risk of distant metastasis also increases with the number of regional nodes involved
  • 27. CLINICAL PRESENTATION AND DIAGNOSIS  Most patients with anal cancer are first seen with rectal bleeding. This occurs in approximately 50% of patients;  30% experience pain or the sensation of a rectal mass.  Pruritus in 30%  Altered bowel habbits -rare  A common concern with most anal neoplasms is the frequent delay in diagnosis resulting from confusion with more common, benign conditions. Thus, the clinician must maintain a high index of suspicion when evaluating lesions of the anal canal and margin.  An interval of 4 to 6 months may ensue between onset of symptoms and diagnosis in up to 50% of patients.
  • 28. WORK UP  Physical examination 1. Regional lymph nodes 2. Adjacent organs for direct invasion 3. Anogenital areas for concurrent malignancies  Proctoscopy &Biopsy of primary tumor  Fine-needle aspiration biopsy or simple excision of enlarged inguinal nodes  Chest radiograph  CT/MRI of abdomen and pelvis( mri preferrd as delineates soft tissue planes better and also better to detect involvement of urethra or vagina)  HIV antibody assay, if risk factors are present
  • 29.  EUS to evaluate for sphincter involvement and perianal lymph nodes.  Consider PET scan since 25% of patients have metastatic disease by PET not seen on CT and 20% of inguinal nodes negative by CT are PET positive.
  • 30. STAGING  PRIMARY TUMOR (T)  TX Primary tumor cannot be assessed  T0 No evidence of primary tumor  Tis Carcinoma in situ  T1 Tumor =2 cm in greatest dimension  T2 Tumor >2 cm but =5 cm in greatest dimension  T3 Tumor >5 cm in greatest dimension  T4 Tumor of any size invades adjacent organ(s) (e.g., vagina, urethra, bladder)  Direct invasion of the rectal wall, perirectal skin, subcutaneous tissue, or the sphincter muscle(s) is not classified as T4
  • 31.  REGIONAL LYMPH NODES (N)  NX Regional lymph nodes cannot be assessed  N0 No regional lymph node metastasis  N1 Metastasis in perirectal lymph node(s)  N2 Metastasis in unilateral internal iliac and/or inguinal lymph node(s)  N3 Metastasis in perirectal and inguinal lymph nodes and/or bilateral internal iliac and/or inguinal lymph node
  • 32. AJCC stage groups  Stage I T1 N0 M0  Stage II T2 N0 M0 T3 N0 M0  Stage IIIA T1 N1 M0 T2 N1 M0 T3 N1 M0 T4 N0 M0  Stage IIIB T4 N1 M0 Any T N3 M0 Any T N2 M0  Stage IV Any T Any N M1
  • 33.
  • 34.
  • 35.
  • 36. PROGNOSIS  5 y survival- T1 — 86 percent T2 — 86 percent T3 — 60 percent T4 — 45 percent N0 — 76 percent N+ — 54 percent
  • 37. Molecular prognostic factors  High expression of p53 associated with decreased DFS.  Also local control rates are lower with increased p53 expression.  High level of Ki 67 – longer DFS.
  • 39. Surgery  Surgical treatment was the primary therapy 20 to 35 years ago, but it has been replaced by sphincter-sparing therapy with combination chemoradiotherapy.  Surgical therapy is now used most often as a method of salvage.  Surgical treatment, when it was used as a primary therapy, required an abdominoperineal resection (APR).  This consisted of wide local excision of the anus, to include the levator ani muscles and contents of the ischiorectal fossa.  The operation results in a permanent colostomy, as well as loss of sexual function, in most patients.  Overall, 5-year survival rates were approximately 50-70% in different serieses.
  • 40.
  • 41.
  • 42.
  • 43. Radical resection  For intermediate-stage primary anal canal cancer who - - Cannot tolerate radiation therapy or chemoradiation - Incontinent because of irreversible damage of the sphincters - Anovaginal fistula - Prior pelvic radiation treatment (most frequently for carcinoma of the cervix) - Active inflammatory bowel disease affecting the rectum or anal region - Failure of chemoradiation or radiation and less frequently, complications of the initial treatment.
  • 44. Residual cancer  Suspected residual cancer should be confirmed by biopsy.  Random biopsies from the site of the primary cancer in the absence of clinical features .  Residual masses after radiation or chemoradiation may take several months to regress fully.  Frequent examination by an experienced observer is desirable, including, if necessary, examination under anesthesia.  C/F - hard-edged ulcer - an enlarging mass - increasing pain
  • 45. SALVAGE SURGERY  Locoregional failure in 30% ½ recurrence, ½ progression Salvage APR is associated with five- year survival rates from 24 to 58%  Salvage Surge APR = abdominoperineal resection Pelvic exenteration = multiviseral resection  Urinary and fecal diversion
  • 46. RECURRENCES  Strictly, all local recurrences are due to residual cancer.  Salvage surgery offers a potential for long-term local control and survival in roughly one third to one half of the patients fit for surgery who do not have clearly unresectable cancer or known extrapelvic disease.  Need reconstructive surgery to close defects in irradiated pelvic tissues should be considered.
  • 47. Prognostic variables  Node positivity  Size of the resected tumor  Status of resection margins  An analysis of the pathologic data from patients in the UKCCCR trial showed – lateral excision margin free of cancer > 1 mm - recurrence occurred in 25% < 1mm - recurrence occurred in
  • 48. Problems in Surgery  Perineal wound healing  skin breakdown  fistula formation,  Malnutrition  Debility due to pain  Flap reconstruction should be considered
  • 49. TREATMENT OF LYMPHATICS  Lymphatic Drainage Lymphatic drainage of anal cancers depends on the location of the tumor in relation to the dentate line. Tumors below the dentate line drain to the inguinal and femoral nodes. Tumors above the dentate line drain to the perirectal and paravertebral nodes, a pattern similar to that seen with rectal cancers. Tumors in the most proximal portion of the canal drain to the nodes of the inferior mesenteric system.
  • 50. Lymph Node Management  Chemoradiation is the treatment of choice for inguinal lymph node disease Cure rates approach 90 percent for synchronous disease Bilateral groins should be incorporated into the radiation fields with the addition of a boost for clinically positive lymph nodes. Metachronous lymph nodes + in 10 to 20% Usually appearing w/in six months after treatment Respond well to CRT  Formal node dissection is reserved for metastases residual or recurrent after radiation-based treatment.
  • 51. CLINICALLY NORMAL NODES  If dissected - significant postoperative wound healing problems or chronic lymphedema.  Rate of late failure in clinically normal inguinal nodes not treated prophylactically ranges from about 10% to 25%.  May prove uncontrollable in up to one half of the patients.  Because of the morbidity - elective lymphadenectomy of clinically normal inguinal nodes is not recommended.  Elective irradiation of clinically normal inguinal node areas - little morbidity - reduces the risk of late node failure in the volume irradiated to less than 5%
  • 52. Sentinel Lymph Node Bx  SLNB identifies inguinal metastases in 10–40% of anal cancer patients with limited morbidity ranging between 3% and 7%. The clinical impact of this procedure on the therapeutic approach is unclear as long as the inguinal nodes are included in the radiation field.
  • 53. APR
  • 54. The Technique Pre-operative  Consent  Bowel preparation  Stomal therapy and siting for stoma  DVT prophylaxis  Antibiotics  Urinary catheter
  • 55. The Technique Set-up  Extended Lloyd-Davies position  Good assistance  Long midline incision  Wide retraction  Small bowel packed out of the way  Full laparotomy (liver etc)
  • 57. TME Principle is that the sharp dissection(diathermy/ scissors) should only proceed in the areolar tissue plane(holy plane) within and thus sparing the autonomic nerve plexuses, the non visceral presacral fat pad, the parietal sidewall fascia of the pelvis, the hypogastric plexus, vesicles and prostate in males and vagina in females.
  • 58.
  • 59.  The sigmoid is grasped with toothed forceps and reflected medially The adjacent adhesive bands are divided with long curves scissors, and the peritoneal reflection is retracted laterally with forceps. Following this procedure, the sigmoid is usually mobilized easily toward the midline. The peritoneal surface on the left side of the colon is picked up with forceps and divided with long, curved, blunt-nosed Metzenbaum scissors, which are gently introduced downward beneath the peritoneum to separate the underlying structures, such as the left spermatic, or ovarian, vessels or ureter, from the peritoneum to avoid their accidental injury. The peritoneum is incised down to the cul-de-sac on the left side
  • 60.
  • 61.
  • 62. APR
  • 63.  The inferior mesenteric vein is often divided above the left colic branch and a mobilization of the splenic flexure is performed so as to allow creation of the descending colostomy without tension. The blood supply to the descending colon is now derived from the middle colic artery via the marginal artery of Drummond.
  • 65.  Although involved lymph nodes may not be evident in the mesentery over the bifurcation of the aorta, it is desirable to ligate the inferior mesenteric artery just distal to the origin of the left colic artery . The contents of the proximal clamps are tied, and the ligation is reinforced by a transfixing suture.  Some prefer to ligate the inferior mesenteric artery as near its point of origin from the aorta as possible. Usually, this level is near the ligament of Treitz. The blood supply to the sigmoid to be used as a colostomy is now derived from the middle artery through the marginal artery of Drummond.
  • 67.
  • 68.  The peritoneum along the right side of the rectosigmoid junction is incised lateral to the inferior mesenteric and superior hemorrhoidal vessels .
  • 69.  This incision extends down to the pouch of Douglas. The right ureter is identified beneath the residual peritoneum, and its course over the iliac vessels is exposed with blunt gauze dissection. The proximal bowel is retracted anteriorly and laterally. The superior hypogastric nerves are visualized just below the iliac vessels and the ureters. The dissection proceeds behind the superior hemorrhoidal vessels toward the entrance of the presacral space behind the sacral promontory. Division of the retrosacral fascia or ligament just below the sacral curvature at about S2 is done sharply in the midline with scissors or electrocautery.
  • 70.  The peritoneal reflection in the pouch of Douglas is incised about 1 cm up its anterior reflection over the bladder in men (shown in this illustration) or behind the uterus in women. The bladder or uterus is retracted anteriorly using a fiberoptic lighted deep pelvic retractor. The sharp dissection proceeds anterior to Denonvilliers' fascia until the prostate and seminal vessels or the rectovaginal septum is seen.
  • 71.  The paths of the anterior and posterior dissections (Figure 9) show the close adherence to the presacral fascia posteriorly and to the actual prostate and seminal vesicles anteriorly.
  • 72.  The two lateral dissections in the TME are time- consuming, as the surgeon carefully proceeds to expose the parietal fascia over the lateral pelvic wall structures.  The fiberoptic lighted deep pelvic retractors are essential for clear visualization during lateral retraction of the rectum and anterior elevation of the bladder or the uterus and vagina.  The preservation of the pelvic autonomic nerve plexus and the anterior roots of sacral nerves S2, S3, and S4 is essential for anal continence and sexual function. The plexus is seen as a dense plaque of nerve tissue that comes close to the rectum at the level of the prostate or upper vagina
  • 73.  . The TME does not encounter "lateral suspensory ligaments" but rather a fusion of the lateral mesorectum with tissue that may contain the middle hemorrhoidal arteries as the dissection heads toward the autonomic nerve plexus.  This tissue is divided with electrocautery, and the middle hemorrhoidal vessels may require a ligature. The course of the ureters and the autonomic plexus is noted as the dissection is carried down to the levators
  • 74.
  • 75.
  • 79.
  • 80.
  • 81.
  • 82.
  • 83.
  • 84.
  • 85.
  • 87.
  • 88.  The skin in the region of the anal orifice is seized with several Allis forceps, and the incision is made through the skin and subcutaneous tissue at least 2 cm away from the closed anal orifice
  • 89.  All blood vessels are clamped and tied to prevent further loss of blood as the operation progresses
  • 90.  he posterior portion of the incision is extended backward over the coccyx, and the anus is tipped upward to enable its attachments to the coccyx to be severed more readily. After the anococcygeal raphe is severed and the presacral space is entered, the accumulated blood from above is suctioned out.
  • 91.  The levator muscle is exposed on one side and, with the finger held beneath it, is divided between paired clamps as far from the rectum as possible.Following the ligation of all bleeding points on one side, a similar division of the levator ani muscles is carried out on the opposite side. Alternatively, the levator muscles may be transected with electrocautery.
  • 92.  Palpation of the inlying urethral catheter will facilitate the procedure by localizing the urethra and preventing accidental injury to the prostate, urethra. The skin and subcutaneous tissue of the perineum are retracted upward, while the anus is pulled downward and backward to assist in the exposure. The rectum is pulled down, the remaining attachments of the levator ani muscles and transversus perinea are divided, and all bleeding points are ligated
  • 93.  . In the female the dissection between the rectum and vagina is more easily accomplished if counterresistance is applied to the posterior vaginal wall by the surgeon's fingers. In the presence of extensive infiltrating growths it may be necessary to excise the perineal body as well as a portion of the posterior vaginal wall.
  • 94.
  • 95.
  • 96.
  • 98. Anal Margin Cancers  Anal margin -distal end of the anal canal to a 5- cm margin surrounding the verge.  Treat similar to skin cancer.  WLE for T1 and early T2 lesions that can be excised with a 1-cm margin.  Larger T2 cancers -add prophylactic radiation to the inguinal lymph nodes along with radiation or excision of the primary tumor.  T3 and T4 lesions- radiation to both inguinal regions and the pelvis, along with 5-FU and mitomycin C.  APR for bulky tumors extending into the sphincter or surrounding structures.
  • 99.  When possible, initial surgical management is preferred to radiation- based treatment of perianal cancers because of the frequent morbidity from long-term changes in the perianal skin after irradiation.
  • 100.  The regional nodes for the perianal skin are the inguinal nodes.  Perirectal or pelvic node metastases are very uncommon.  The risk of inguinal node metastases is about 10%, associated mainly with category T3 or T4 tumors, or poorly differentiated cancers.  Elective inguinal nodal irradiation has been suggested for those categories only.  The management of abnormal inguinal nodes is similar to that of anal canal cancer.