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ORAL MANIFESTATIONS IN HIV
DISEASE
VIRUS PARTICLE
VIRAL REPLICATION
 Methods of transmission:
 Sexual transmission, presence of STD increases
likelihood of transmission.
 Exposure to infected blood or blood products.
 Use of contaminated clotting factors by
hemophiliacs.
 Sharing contaminated needles (IV drug users).
 Transplantation of infected tissues or organs.
 Mother to fetus, perinatal transmission variable,
dependent on viral load and mother’s CD 4
count.
TRANSMISSION
PRIMARY HIV SYNDROME
 Mononucleosis-like, cold or flu-like
symptoms may occur 6 to 12 weeks after
infection.
 lymphadenopathy
 fever
 rash
 headache
 Fatigue
 diarrhea
 sore throat
 neurologic manifestations.
 no symptoms may be present
PRIMARY HIV SYNDROME
 Symptoms are relatively nonspecific.
 HIV antibody test often negative but
becomes positive within 3 to 6 months,
this process is known as
seroconversion.
 Large amount of HIV in the peripheral
blood.
 Primary HIV can be diagnosed using viral
load titer assay or other tests.
 Primary HIV syndrome resolves itself and
HIV infected person remains asymptomatic
for a prolonged period of time, often years.
CLINICAL LATENCY PERIOD
 HIV continues to reproduce, CD4 count
gradually declines from its normal value of
500-1200.
 Once CD4 count drops below 500, HIV
infected person at risk for opportunistic
infections.
 The following diseases are predictive of the
progression to AIDS:
 persistent herpes-zoster infection (shingles)
 oral candidiasis (thrush)
 oral hairy leukoplakia
 Kaposi’s sarcoma (KS)
AIDS
 CD4 count drops below 200 person is considered to
have advanced HIV disease
 If preventative medications not started the HIV
infected person is now at risk for:
 Pneumocystis carinii pneumonia (PCP)
 cryptococcal meningitis
 toxoplasmosis
 If CD4 count drops below 50:
 Mycobacterium avium
 Cytomegalovirus infections
 lymphoma
 dementia
 Most deaths occur with CD4 counts below 50.
OTHER OPPORTUNISTIC INFECTIONS
 Respiratory system
 Pneumocystis Carinii Pneumonia (PCP)
 Tuberculosis (TB)
 Kaposi's Sarcoma (KS)
 Gastro-intestinal system
 Cryptosporidiosis
 Candida
 Cytomegolavirus (CMV)
 Isosporiasis
 Kaposi's Sarcoma
 Central/peripheral Nervous system
 Cytomegolavirus
 Toxoplasmosis
 Cryptococcosis
 Non Hodgkin's lymphoma
 Varicella Zoster
 Herpes simplex
 Skin
 Herpes simple
 Kaposi's sarcoma
 Varicella Zoster
Oral manifestations of HIV
i. Saliva substitutes – these include water, artificial salivas – mucin based ,
carboxymethylcellulose based
ii. Saliva stimulants – organic acids – ascorbic acid and malic acid
iii. chewing gum
iv. parasympathomimetic drugs (choline esters, e.g. pilocarpine
hydrochloride,cholinesterase inhibitors and other substances (sugar-free
mints, nicotinamide
CANDIDIASIS
2 Weeks with treatment
The condition often resolves rapidly with high dose acyclovir but recurs once this
therapy is stopped, or as the underlying immunocompromise worsens.
Topical use of podophyllum resin or retinoids has also been reported to produce
temporary remission.
Antiretroviral drugs such as zidovudine may be effective in producing a significant
regression of OHL.
Recurrence of the lesion may also signify that highly active antiretroviral
therapy (HAART) is becoming ineffective
Vinblastine sulphate for
treatment
KAPOSI’S SARCOMA (KS)
 Kaposi’s sarcoma (shown)
is a rare cancer of the
blood vessels that is
associated with HIV. It
manifests as bluish-red
oval-shaped patches that
may eventually become
thickened. Lesions may
appear singly or in
clusters.
Topical 5 flurouracil
 Topical corticosteroids
 Dexamethasone- 0.5mg/5ml for 1 min – 2- 3 times
daily
 Predisone
Oral manifestations in hiv disease

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Oral manifestations in hiv disease

  • 3. VIRAL REPLICATION  Methods of transmission:  Sexual transmission, presence of STD increases likelihood of transmission.  Exposure to infected blood or blood products.  Use of contaminated clotting factors by hemophiliacs.  Sharing contaminated needles (IV drug users).  Transplantation of infected tissues or organs.  Mother to fetus, perinatal transmission variable, dependent on viral load and mother’s CD 4 count.
  • 4.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10. PRIMARY HIV SYNDROME  Mononucleosis-like, cold or flu-like symptoms may occur 6 to 12 weeks after infection.  lymphadenopathy  fever  rash  headache  Fatigue  diarrhea  sore throat  neurologic manifestations.  no symptoms may be present
  • 11.
  • 12. PRIMARY HIV SYNDROME  Symptoms are relatively nonspecific.  HIV antibody test often negative but becomes positive within 3 to 6 months, this process is known as seroconversion.  Large amount of HIV in the peripheral blood.  Primary HIV can be diagnosed using viral load titer assay or other tests.  Primary HIV syndrome resolves itself and HIV infected person remains asymptomatic for a prolonged period of time, often years.
  • 13. CLINICAL LATENCY PERIOD  HIV continues to reproduce, CD4 count gradually declines from its normal value of 500-1200.  Once CD4 count drops below 500, HIV infected person at risk for opportunistic infections.  The following diseases are predictive of the progression to AIDS:  persistent herpes-zoster infection (shingles)  oral candidiasis (thrush)  oral hairy leukoplakia  Kaposi’s sarcoma (KS)
  • 14. AIDS  CD4 count drops below 200 person is considered to have advanced HIV disease  If preventative medications not started the HIV infected person is now at risk for:  Pneumocystis carinii pneumonia (PCP)  cryptococcal meningitis  toxoplasmosis  If CD4 count drops below 50:  Mycobacterium avium  Cytomegalovirus infections  lymphoma  dementia  Most deaths occur with CD4 counts below 50.
  • 15.
  • 16.
  • 17. OTHER OPPORTUNISTIC INFECTIONS  Respiratory system  Pneumocystis Carinii Pneumonia (PCP)  Tuberculosis (TB)  Kaposi's Sarcoma (KS)  Gastro-intestinal system  Cryptosporidiosis  Candida  Cytomegolavirus (CMV)  Isosporiasis  Kaposi's Sarcoma  Central/peripheral Nervous system  Cytomegolavirus  Toxoplasmosis  Cryptococcosis  Non Hodgkin's lymphoma  Varicella Zoster  Herpes simplex  Skin  Herpes simple  Kaposi's sarcoma  Varicella Zoster
  • 18.
  • 20.
  • 21.
  • 22. i. Saliva substitutes – these include water, artificial salivas – mucin based , carboxymethylcellulose based ii. Saliva stimulants – organic acids – ascorbic acid and malic acid iii. chewing gum iv. parasympathomimetic drugs (choline esters, e.g. pilocarpine hydrochloride,cholinesterase inhibitors and other substances (sugar-free mints, nicotinamide
  • 23.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29. 2 Weeks with treatment
  • 30.
  • 31. The condition often resolves rapidly with high dose acyclovir but recurs once this therapy is stopped, or as the underlying immunocompromise worsens. Topical use of podophyllum resin or retinoids has also been reported to produce temporary remission. Antiretroviral drugs such as zidovudine may be effective in producing a significant regression of OHL. Recurrence of the lesion may also signify that highly active antiretroviral therapy (HAART) is becoming ineffective
  • 32.
  • 33.
  • 34.
  • 36. KAPOSI’S SARCOMA (KS)  Kaposi’s sarcoma (shown) is a rare cancer of the blood vessels that is associated with HIV. It manifests as bluish-red oval-shaped patches that may eventually become thickened. Lesions may appear singly or in clusters.
  • 37.
  • 39.
  • 40.
  • 41.
  • 42.
  • 43.
  • 44.
  • 45.  Topical corticosteroids  Dexamethasone- 0.5mg/5ml for 1 min – 2- 3 times daily  Predisone