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Rebecca Stoner1
, Joanne Cunningham2
and Adnan Qureshi3
*
1
Department of Colorectal Surgery, Milton Keynes University Hospital NHS Trust, UK
2
Department of Pathology, Milton Keynes University Hospital NHS Trust, UK
3
Department of Colorectal Surgery, Milton Keynes University Hospital NHS Trust, UK
*Corresponding author: Adnan Qureshi, Department of Pathology and Colorectal Surgery, Milton Keynes University Hospital NHS Trust, UK
Submission: April 11, 2018; Published: April 30, 2018
Rapid Cutaneous Metastases from
a Rectal Primary: A Case Report
Introduction
This case report discusses the rapid metastases of a rectal
carcinoma to the skin and liver soon after curative resection of
primary tumour. Cutaneous metastases from gastrointestinal
malignancy are rare, and has been observed in 4-6% of colorectal
adenocarcinoma cases [1,2]. When these cancers do metastasise to
the skin, they mostly present as firm, painless and discrete nodules
[2].
Thereareseveralmechanismsofcutaneousmetastasisintheory,
ranging from direct implantation to lymphatic or haematogenous
spread [3,4]. There are at least 25 case reports in English literature
on cutaneous colorectal metastasis to date.
This case is rare because it was stage 3 colorectal
adenocarcinoma with curative resection, and developed cutaneous
metastasis within 5 weeks of original surgery, leaving one to
suspect that metastasis can present that early and quickly even
after curative surgery.
Further studies and tumour type behaviour is needed in future
to determine these high risk colorectal adenocarcinoma with
potential of early widespread metastases.
Case Report
The patient was a 47 year old lady with severe learning
difficulties due to cerebral palsy with a performance status of
four, due to contractures of the upper and lower limbs, rendering
her immobile. She was admitted under the emergency surgery
team with a single episode of rectal bleeding and a palpable rectal
mass. She underwent examination under anaesthesia and flexible
sigmoidoscopy. Histology from biopsies confirmed a moderately
differentiated adeno carcinoma of the rectum.
A staging CT and MRI scan revealed a tumour in the left lateral
position involving the mid and lower rectum extending into
muscularis propria. No extra luminal disease or lymphadenopathy
was identified. Final radiological staging was Duke’s stage B,
T2N0M0. She underwent surgery with curative intent during the
same admission.
The patient had an APER due to technical reasons caused by her
limb contractures. Post-operative histology showed a tumour size
of 47mm, 3 out of the 20 lymph nodes sampled were found to be
positive. One lymph node was found very close to the circumference
margin anteriorly at 0.1mm, thus making it a R1 resection. The
Case Report
Surgical Medicine Open
Access JournalC CRIMSON PUBLISHERS
Wings to the Research
1/3Copyright © All rights are reserved by Adnan Qureshi.
Volume 1 - Issue - 4
Abstract
The development of cutaneous metastases from gastrointestinal malignancies are rare, but they have been previously reported secondary to
primary colorectal adenocarcinoma in relation to advanced disease. This case report describes a phenomenon of rapidly developing cutaneous and
liver metastases within weeks, from a stage 3 rectal adeno carcinoma operated with curative intent.
A literature review of similar cases was made and contrasted to the rapidity and stage of this aggressive tumour. The current guidelines are also
reflected on, as well as the rate of recurrence with different modalities of treatment.
Keywords: Rectal carcinoma; Cutaneous metastases; Gastrointestinal malignancies; Adenocarcinoma; Liver metastases
ISSN 2578-0379
Surg Med Open Acc J Copyright © Adnan Qureshi
2/3
How to cite this article: Rebecca S, Joanne C, Adnan Q. Rapid Cutaneous Metastases from a Rectal Primary: A Case Report. Surg Med Open Acc J. 1(4).
SMOAJ.000519.2018. DOI: 10.31031/SMOAJ.2018.01.000519
Volume 1 - Issue - 4
longitudinal margins were clear. Histology showed perineural
invasion but no evidence of vascular invasion. Final staging was
moderately differentiated adenocarcinoma rectum with focal areas
of poor differentiation, Dukes C1, T2N1M0 (Figure 1A). It was
decided that the patient was not for further adjuvant treatment due
to performance status.
Figure 1: A: Moderately differentiated adenocarcinoma of the
rectum. B: Skin showing a solid dermal nodule comprising
poorly differentiated adenocarcinoma cells. C: Liver which
is infiltrated by poorly differentiated adenocarcinoma. D:
CK20 immuno histochemistry on the liver shows strong
cytoplasmic expression. E: CDX2 immuno histochemistry
on the liver shows patchy strong nuclear expression.
The patient had a smooth recovery and was awaiting social
input. However, five weeks post operatively she was found clinically
to be septic with a raised white blood cell count and C-reactive
protein. She was treated empirically with antibiotics for suspected
sepsis.
Figure 2A: Multiple Liver Metastases.
Figure 2B: Two cutaneous Metastatic nodules.
Clinically, she developed two enlarged lymph nodes in the
posterior triangle of the neck, left supra clavicular fossa and left
axilla. ACT scan was performed to look for source of sepsis the
scan showed, enhancing nodules in the subcutaneous fat and in
the gluteal muscles with multiple hypoechoic liver lesions and
peritoneal deposits, suspected to be metastatic disease (Figure 2).
Figure 2C: Deep subcutaneous metastatic deposits.
Biopsy of a liver and skin lesion were performed. Both
histology samples were reported as being poorly differentiated
adenocarcinoma (Figure 1B & 1C). Immuno histochemistry showed
the tumour cells expressed CK20 and CDX2 (Figure 1D & 1E). They
were negative for CK7. These were in keeping with metastatic
poorly differentiated adenocarcinoma from a colorectal primary.
The patient was seen by the palliative team after discussion
with her family and was moved to a hospice where she passed
away due to metastatic disease within 8 weeks after the surgery
for moderately differentiated adenocarcinoma stage 3, where
prognosis is normally in years.
Discussion
A study by Abrahms, et al. [5] observing the metastases
at autopsy in 1000 patients found that the commonest site of
metastasis for rectal carcinoma is the liver 47% followed by the lung
at 38%. Only 3% were found to have skin metastasis [1,5]. Brown
and Clark quotes 58.8% of their patients with rectal cancer have
no metastases, though they reflected on the fact that a significant
number of their patients did not survive long past resection or
colostomy formations [6].
Risk of extra-nodal metastases is up to 20% for stage I and II
colorectal cancers within 5 years of surgery [7]. Isolated tumour
cells in regional lymph nodes have been implicated [8], and it is
recommended that at least 12 to 15 lymph nodes be sampled for
regional staging [9].
There have been other cases of rectal adenocarcinoma with
cutaneous metastasis in the literature. Our case is unique as the
patientdevelopedcutaneousmetastasiswithinfiveweeksofcurative
surgery. A similar case reported in the literature which describes
a 55 year old gentleman with T3N2M0 rectal adenocarcinoma
presenting 18 months following surgery and chemotherapy, with
subcutaneous metastatic nodules [10]. A similar phenomenon
3/3
How to cite this article: Rebecca S, Joanne C, Adnan Q. Rapid Cutaneous Metastases from a Rectal Primary: A Case Report. Surg Med Open Acc J. 1(4).
SMOAJ.000519.2018. DOI: 10.31031/SMOAJ.2018.01.000519
Surg Med Open Acc J Copyright © Adnan Qureshi
Volume 1 - Issue - 4
described by Wang et al. [11] in a 76 year old lady with T4aN1Mx
poorly differentiated adenocarcinoma with lymph node metastasis,
also developed subcutaneous nodules on the patient’s back [11].
This occurred within one month of surgery, in this case report the
patient already had locally advanced T4 disease with unmapped
metastasis, necessitating neo adjuvant chemotherapy which was
not administered due to impending bowel obstruction. Another
case reporting a 44 year old lady who presented with a number of
well defined, painless subcutaneous nodules which were found to
be metastases , from a primary T4 N2 M1 ,sigmoid adenocarcinoma
[12].
Current guidelines do not recommend adjuvant chemotherapy
for stage 2 disease [13]. A retrospective study observing patients
with T1 and T2 disease treated by local excision alone found that
37% of patients with T2 disease, had a recurrence at 54 months
post op, with the average time being 18 months [14,15].
This case is unique in that metastases to both skin and
liver occurred within 5 weeks of curative surgery for a stage 3
predominantly moderately differentiated rectal adenocarcinoma
which developed rapidly following surgery. The exact mechanism
to which cutaneous metastases from rectal carcinoma occurs is
uncertain, and further research is needed to determine the risk
factors for this.
References
1.	 Lookingbill DP, Spangler N, Helm KF (1993) Cutaneous metastases
in patients with metastatic carcinoma: A retrospective study of 4020
patients. J Am Acad Dermatol 29(2): 228-236.
2.	 Guanziroli E, Coggi A, Venegoni L, Fanoni D, Ercoli G, et al. (2017)
Cutaneous metastases of internal malignancies: An experience from a
single institution. Eur J Dermatol 27(6): 609-614.
3.	 Royston D, David G Jackson (2009) Mechanisms of lymphatic metastasis
in human colorectal adenocarcinoma. The Journal of Pathology 217(5):
608-619.
4.	 Weiss L, Grundmann E, Torhorst J, Hartveit F, Moberg I, et al. (1986)
Haematogenous metastastic patterns in colonic carcinoma: An analysis
of 1541 necropsies. J Pathol 150(3): 195-203.
5.	 Abrams HL, Spiro R, Goldstein N (1950) Metastases in carcinoma.
Analysis of 1000 autopsied cases. Cancer 3(1): 74-85.
6.	 Brown CE, Warren S (1938) Visceral metastasis from rectal carcinoma.
Surg Gynecol Obstet 66: 611-621.
7.	 Bilchik A, Nissan A, Wainberg Z, Shen P, McCarter M, et al. (2010) Surgical
quality and nodal ultrastaging is associated with long-term disease-
free survival in early colorectal cancer: An analysis of 2 international
multicenter prospective trials. Ann Surg 252(3): 467-474; discussion
474-476.
8.	 Mescoli C, Albertoni L, Pucciarelli S, Giacomelli L, RussoVM, et al. (2012)
Isolated tumor cells in regional lymph nodes as relapse predictors in
stage I and II colorectal cancer. J Clin Oncol 30(9): 965-971.
9.	 Compton CC, Fielding LP, Burgart LJ, Conley B, Cooper HS, et al. (2000)
Prognostic factors in colorectal cancer.College of american pathologists
consensus statement 1999. Arch Pathol Lab Med 124(7): 979-994.
10.	de Miguel Valencia MJ, Fraile Gonzalez M, Yague Hernando A, Oteiza
Martinez F, Ciga Lozano MA (2013) Cutaneous metastases of rectal
cancer. Anales Del Sistema Sanitario De Navarra 36(3): 557-561.
11.	Wang DY, Feng Ye, Jian Jiang Lin, Xiao Xu (2017) Cutaneous metastasis:
A rare phenomenon of colorectal cancer. Ann Surg Treat Res 93(5): 277-
280.
12.	Llaguna OH, Desai P, Fender AB, Zedek DC, Meyers MO, et al. (2010)
Subcutaneous metastatic adenocarcinoma: An unusual presentation of
colon cancer - case report and literature review. Case Rep Oncol 3(3):
386-390.
13.	Benson AB 3rd
, Schrag D, Somerfield MR, Cohen AM, Figueredo AT, et
al. (2004) American society of clinical oncology recommendations on
adjuvant chemotherapy for stage II colon cancer. J Clin Oncol 22(16):
3408-3419.
14.	Garcia Aguilar J, Mellgren A, Sirivongs P, Buie D, Madoff RD, et al. (2000)
Local excision of rectal cancer without adjuvant therapy: a word of
caution. Ann Surg 231(3): 345-351.
15.	Gmitter TL, Dhawan SS, Phillips MG, Wiszniak J (1990) Cutaneous
metastases of colonic adenocarcinoma. Cutis 46(1): 66-68.
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Rapid Cutaneous Metastases from a Rectal Primary: A Case Report

  • 1. Rebecca Stoner1 , Joanne Cunningham2 and Adnan Qureshi3 * 1 Department of Colorectal Surgery, Milton Keynes University Hospital NHS Trust, UK 2 Department of Pathology, Milton Keynes University Hospital NHS Trust, UK 3 Department of Colorectal Surgery, Milton Keynes University Hospital NHS Trust, UK *Corresponding author: Adnan Qureshi, Department of Pathology and Colorectal Surgery, Milton Keynes University Hospital NHS Trust, UK Submission: April 11, 2018; Published: April 30, 2018 Rapid Cutaneous Metastases from a Rectal Primary: A Case Report Introduction This case report discusses the rapid metastases of a rectal carcinoma to the skin and liver soon after curative resection of primary tumour. Cutaneous metastases from gastrointestinal malignancy are rare, and has been observed in 4-6% of colorectal adenocarcinoma cases [1,2]. When these cancers do metastasise to the skin, they mostly present as firm, painless and discrete nodules [2]. Thereareseveralmechanismsofcutaneousmetastasisintheory, ranging from direct implantation to lymphatic or haematogenous spread [3,4]. There are at least 25 case reports in English literature on cutaneous colorectal metastasis to date. This case is rare because it was stage 3 colorectal adenocarcinoma with curative resection, and developed cutaneous metastasis within 5 weeks of original surgery, leaving one to suspect that metastasis can present that early and quickly even after curative surgery. Further studies and tumour type behaviour is needed in future to determine these high risk colorectal adenocarcinoma with potential of early widespread metastases. Case Report The patient was a 47 year old lady with severe learning difficulties due to cerebral palsy with a performance status of four, due to contractures of the upper and lower limbs, rendering her immobile. She was admitted under the emergency surgery team with a single episode of rectal bleeding and a palpable rectal mass. She underwent examination under anaesthesia and flexible sigmoidoscopy. Histology from biopsies confirmed a moderately differentiated adeno carcinoma of the rectum. A staging CT and MRI scan revealed a tumour in the left lateral position involving the mid and lower rectum extending into muscularis propria. No extra luminal disease or lymphadenopathy was identified. Final radiological staging was Duke’s stage B, T2N0M0. She underwent surgery with curative intent during the same admission. The patient had an APER due to technical reasons caused by her limb contractures. Post-operative histology showed a tumour size of 47mm, 3 out of the 20 lymph nodes sampled were found to be positive. One lymph node was found very close to the circumference margin anteriorly at 0.1mm, thus making it a R1 resection. The Case Report Surgical Medicine Open Access JournalC CRIMSON PUBLISHERS Wings to the Research 1/3Copyright © All rights are reserved by Adnan Qureshi. Volume 1 - Issue - 4 Abstract The development of cutaneous metastases from gastrointestinal malignancies are rare, but they have been previously reported secondary to primary colorectal adenocarcinoma in relation to advanced disease. This case report describes a phenomenon of rapidly developing cutaneous and liver metastases within weeks, from a stage 3 rectal adeno carcinoma operated with curative intent. A literature review of similar cases was made and contrasted to the rapidity and stage of this aggressive tumour. The current guidelines are also reflected on, as well as the rate of recurrence with different modalities of treatment. Keywords: Rectal carcinoma; Cutaneous metastases; Gastrointestinal malignancies; Adenocarcinoma; Liver metastases ISSN 2578-0379
  • 2. Surg Med Open Acc J Copyright © Adnan Qureshi 2/3 How to cite this article: Rebecca S, Joanne C, Adnan Q. Rapid Cutaneous Metastases from a Rectal Primary: A Case Report. Surg Med Open Acc J. 1(4). SMOAJ.000519.2018. DOI: 10.31031/SMOAJ.2018.01.000519 Volume 1 - Issue - 4 longitudinal margins were clear. Histology showed perineural invasion but no evidence of vascular invasion. Final staging was moderately differentiated adenocarcinoma rectum with focal areas of poor differentiation, Dukes C1, T2N1M0 (Figure 1A). It was decided that the patient was not for further adjuvant treatment due to performance status. Figure 1: A: Moderately differentiated adenocarcinoma of the rectum. B: Skin showing a solid dermal nodule comprising poorly differentiated adenocarcinoma cells. C: Liver which is infiltrated by poorly differentiated adenocarcinoma. D: CK20 immuno histochemistry on the liver shows strong cytoplasmic expression. E: CDX2 immuno histochemistry on the liver shows patchy strong nuclear expression. The patient had a smooth recovery and was awaiting social input. However, five weeks post operatively she was found clinically to be septic with a raised white blood cell count and C-reactive protein. She was treated empirically with antibiotics for suspected sepsis. Figure 2A: Multiple Liver Metastases. Figure 2B: Two cutaneous Metastatic nodules. Clinically, she developed two enlarged lymph nodes in the posterior triangle of the neck, left supra clavicular fossa and left axilla. ACT scan was performed to look for source of sepsis the scan showed, enhancing nodules in the subcutaneous fat and in the gluteal muscles with multiple hypoechoic liver lesions and peritoneal deposits, suspected to be metastatic disease (Figure 2). Figure 2C: Deep subcutaneous metastatic deposits. Biopsy of a liver and skin lesion were performed. Both histology samples were reported as being poorly differentiated adenocarcinoma (Figure 1B & 1C). Immuno histochemistry showed the tumour cells expressed CK20 and CDX2 (Figure 1D & 1E). They were negative for CK7. These were in keeping with metastatic poorly differentiated adenocarcinoma from a colorectal primary. The patient was seen by the palliative team after discussion with her family and was moved to a hospice where she passed away due to metastatic disease within 8 weeks after the surgery for moderately differentiated adenocarcinoma stage 3, where prognosis is normally in years. Discussion A study by Abrahms, et al. [5] observing the metastases at autopsy in 1000 patients found that the commonest site of metastasis for rectal carcinoma is the liver 47% followed by the lung at 38%. Only 3% were found to have skin metastasis [1,5]. Brown and Clark quotes 58.8% of their patients with rectal cancer have no metastases, though they reflected on the fact that a significant number of their patients did not survive long past resection or colostomy formations [6]. Risk of extra-nodal metastases is up to 20% for stage I and II colorectal cancers within 5 years of surgery [7]. Isolated tumour cells in regional lymph nodes have been implicated [8], and it is recommended that at least 12 to 15 lymph nodes be sampled for regional staging [9]. There have been other cases of rectal adenocarcinoma with cutaneous metastasis in the literature. Our case is unique as the patientdevelopedcutaneousmetastasiswithinfiveweeksofcurative surgery. A similar case reported in the literature which describes a 55 year old gentleman with T3N2M0 rectal adenocarcinoma presenting 18 months following surgery and chemotherapy, with subcutaneous metastatic nodules [10]. A similar phenomenon
  • 3. 3/3 How to cite this article: Rebecca S, Joanne C, Adnan Q. Rapid Cutaneous Metastases from a Rectal Primary: A Case Report. Surg Med Open Acc J. 1(4). SMOAJ.000519.2018. DOI: 10.31031/SMOAJ.2018.01.000519 Surg Med Open Acc J Copyright © Adnan Qureshi Volume 1 - Issue - 4 described by Wang et al. [11] in a 76 year old lady with T4aN1Mx poorly differentiated adenocarcinoma with lymph node metastasis, also developed subcutaneous nodules on the patient’s back [11]. This occurred within one month of surgery, in this case report the patient already had locally advanced T4 disease with unmapped metastasis, necessitating neo adjuvant chemotherapy which was not administered due to impending bowel obstruction. Another case reporting a 44 year old lady who presented with a number of well defined, painless subcutaneous nodules which were found to be metastases , from a primary T4 N2 M1 ,sigmoid adenocarcinoma [12]. Current guidelines do not recommend adjuvant chemotherapy for stage 2 disease [13]. A retrospective study observing patients with T1 and T2 disease treated by local excision alone found that 37% of patients with T2 disease, had a recurrence at 54 months post op, with the average time being 18 months [14,15]. This case is unique in that metastases to both skin and liver occurred within 5 weeks of curative surgery for a stage 3 predominantly moderately differentiated rectal adenocarcinoma which developed rapidly following surgery. The exact mechanism to which cutaneous metastases from rectal carcinoma occurs is uncertain, and further research is needed to determine the risk factors for this. References 1. Lookingbill DP, Spangler N, Helm KF (1993) Cutaneous metastases in patients with metastatic carcinoma: A retrospective study of 4020 patients. J Am Acad Dermatol 29(2): 228-236. 2. Guanziroli E, Coggi A, Venegoni L, Fanoni D, Ercoli G, et al. (2017) Cutaneous metastases of internal malignancies: An experience from a single institution. Eur J Dermatol 27(6): 609-614. 3. Royston D, David G Jackson (2009) Mechanisms of lymphatic metastasis in human colorectal adenocarcinoma. The Journal of Pathology 217(5): 608-619. 4. Weiss L, Grundmann E, Torhorst J, Hartveit F, Moberg I, et al. (1986) Haematogenous metastastic patterns in colonic carcinoma: An analysis of 1541 necropsies. J Pathol 150(3): 195-203. 5. Abrams HL, Spiro R, Goldstein N (1950) Metastases in carcinoma. Analysis of 1000 autopsied cases. Cancer 3(1): 74-85. 6. Brown CE, Warren S (1938) Visceral metastasis from rectal carcinoma. Surg Gynecol Obstet 66: 611-621. 7. Bilchik A, Nissan A, Wainberg Z, Shen P, McCarter M, et al. (2010) Surgical quality and nodal ultrastaging is associated with long-term disease- free survival in early colorectal cancer: An analysis of 2 international multicenter prospective trials. Ann Surg 252(3): 467-474; discussion 474-476. 8. Mescoli C, Albertoni L, Pucciarelli S, Giacomelli L, RussoVM, et al. (2012) Isolated tumor cells in regional lymph nodes as relapse predictors in stage I and II colorectal cancer. J Clin Oncol 30(9): 965-971. 9. Compton CC, Fielding LP, Burgart LJ, Conley B, Cooper HS, et al. (2000) Prognostic factors in colorectal cancer.College of american pathologists consensus statement 1999. Arch Pathol Lab Med 124(7): 979-994. 10. de Miguel Valencia MJ, Fraile Gonzalez M, Yague Hernando A, Oteiza Martinez F, Ciga Lozano MA (2013) Cutaneous metastases of rectal cancer. Anales Del Sistema Sanitario De Navarra 36(3): 557-561. 11. Wang DY, Feng Ye, Jian Jiang Lin, Xiao Xu (2017) Cutaneous metastasis: A rare phenomenon of colorectal cancer. Ann Surg Treat Res 93(5): 277- 280. 12. Llaguna OH, Desai P, Fender AB, Zedek DC, Meyers MO, et al. (2010) Subcutaneous metastatic adenocarcinoma: An unusual presentation of colon cancer - case report and literature review. Case Rep Oncol 3(3): 386-390. 13. Benson AB 3rd , Schrag D, Somerfield MR, Cohen AM, Figueredo AT, et al. (2004) American society of clinical oncology recommendations on adjuvant chemotherapy for stage II colon cancer. J Clin Oncol 22(16): 3408-3419. 14. Garcia Aguilar J, Mellgren A, Sirivongs P, Buie D, Madoff RD, et al. (2000) Local excision of rectal cancer without adjuvant therapy: a word of caution. Ann Surg 231(3): 345-351. 15. Gmitter TL, Dhawan SS, Phillips MG, Wiszniak J (1990) Cutaneous metastases of colonic adenocarcinoma. Cutis 46(1): 66-68. For possible submissions Click Here Submit Article Creative Commons Attribution 4.0 International License Surgical Medicine Open Access Journal Benefits of Publishing with us • High-level peer review and editorial services • Freely accessible online immediately upon publication • Authors retain the copyright to their work • Licensing it under a Creative Commons license • Visibility through different online platforms