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AIDS
Acquired immunodeficiency syndrome. First reported in 1981. Human immunodeficiency virus. Profound impairment of the immune system (CD4 cell). Increased risk for malignancy, disseminated infections and adverse drug reactions. high quantities of HIV only in blood, semen, and cerebrospinal fluid.
Modes of Transmission
2. Clinical Categories Category A Asymptomatic HIV infection Persistent generalized lymphadenopathy Acute (primary) HIV infection with accompanying illness or history of acute HIV infection
Category B Bacillary angiomatosis Candidiasis, oropharyngeal (thrush) Candidiasis, vulvovaginal; persistent, frequent, or poorly responsive to therapy Cervical dysplasia (moderate or severe)/cervical carcinoma in situ Constitutional symptoms, such as fever (38.5 C) or diarrhea lasting greater than 1 month
Hairy leukoplakia, oral Herpes zoster (shingles), involving at least two distinct episodes or more than one dermatome Idiopathic thrombocytopenic purpura Listeriosis Pelvic inflammatory disease, particularly if complicated by tubo-ovarian abscess Peripheral neuropathy
Category C
Clinical conditions listed in the AIDS surveillance case definition.
Symptoms
Few weeks to months. Acute symptoms-malaise, fatigue, fever, myalgia, erythematous cutaneous eruption, oral candidiasis, oral ulcerations, and thrombocytopenia. Duration - 2 weeks. Seroconversion occurs 3 to 8 weeks later.
Oral Manifestations
Commonly occuring oral candidiasis oral hairy leukoplakia atypical periodontal diseases oral Kaposi's sarcoma, and oral non-Hodgkin's lymphoma Less common - melanotic hyperpigmentation, mycobacterial infections, necrotizing ulcerative stomatitis, miscellaneous oral ulcerations, and viral infections.
Oral Candidiasis
Most common - 90% of AIDS patients. Diminished host resistance debilitated patients , patients receiving immunosuppressive therapy. Oppurtunistic prolonged antibiotic therapy. Most oral candidal infections (85% to 95%) are associated with Candida albicans. Non-C. albicans infections are more common among immunocompromised individuals already receiving antifungal therapy for C. albicans.
Pseudomembranous candidiasis (thrush) painless or slightly sensitive white lesions readily scraped and separated from the surface of the oral mucosa Hard and soft palate and the buccal or labial mucosa
Erythematous candidiasis red patches on the buccal or palatal mucosa associated with depapillation of the tongue Hyperplastic candidiasis least common buccal mucosa and tongue resistant to removal Angular cheilitis commissures appear erythematous surface crusting and fissuring
Diagnosis
microscopic examination of a tissue sample or smear. hyphae and yeast forms.
Treatment
topical and systemic antifungal agents. Amphotericin B oral suspension is more effective against Candida albicans. Ketaconazole-systemic therapy. refractory or recurrent. 30% of AIDS related candidiasis relapse within 4 weeks of treatment and 60% to 80% within 3 months.
EBV-infected but HIV-negative individuals suffering from immunosuppressed conditions (e.g., acute myelogenous leukemia, organ transplantation or extensive systemic corticosteroid therapy). OHL of the tongue in a high-risk patient is considered to be a specific early sign of HIV infection and a strong indicator that the patient will develop AIDS. 83% of HIV-infected patients with hairy leukoplakia would develop AIDS within 31 months, and Nearly 100% of patients with hairy leukoplakia will eventually develop AIDS.
Treatment
Laser or conventional surgery. systemic antiviral agents such as acyclovir.
Kaposis Sarcoma
Multifocal, vascular neoplasm. Probable causative organism-human herpes virus-8 (HHV-8). HIV-infected individuals are 7000fold more likely to develop KS. localized and slowly growing lesion. In HIV individuals - aggressive lesion. Majority (71%) develop lesions of the oral mucosa, particularly the palate and gingiva.
Painless, reddishpurple macules of the mucosa. Nodules, papules, or nonelevated macules that are usually brown, blue, or purple. Microscopic features Atypical vascular channels extravascular hemorrhage with hemosiderin deposition spindle cell proliferation in association mononuclear inflammatory infiltrate consisting mainly of plasma cells
Differential Diagnosis Pyogenic granuloma, hemangioma, atypical hyperpigmentation, sarcoidosis, bacillary angiomatosis, angiosarcoma, pigmented nevi, and cat-scratch disease.
Management Antiretroviral agents, laser excision, radiation therapy, or intralesional injection with vinblastine or interferon a. Tendency to recur. Destructive periodontitis scaling and root planing.
Linear Gingival Erythema persistent, linear, easily bleeding, erythematous gingivitis. localized or generalized; marginal or diffuse. Concomitant oral candidiasisCandida dubliniensis.
Histopathology Increased blood vessels. Lack of infammatory cell infiltrate. Treatment Non-responsive to therapy. Spontaneous remission-some cases. Meticulous oral hygiene. Scaling, irrigation with chlorhexidine. Recall after 2-3 weeks. Persistent cases-treat for candida infection.
Management
Cleaning and debridement. Oral hygiene instructions. Systemic antibiotics-metronidazole and amoxycillin. Re-evaluation after 1 month. Osseous necrosis - remove the affected bone to promote wound healing.