HIV
Kaposi's Sarcoma
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Kaposi's Sarcoma
, Kaposi Sarcoma, Multiple Idiopathic Hemorrhagic Sarcoma
Epidemiology
Highest frequency in HIV homosexual or bisexual men
Middle aged to elderly white males
Young Black patients in Africa
Very uncommon in women and children
Incidence
Was more common (48%) early in the HIV epidemic
Now only seen 18% of HIV cases in homosexual or bisexual men
Pathophysiology
Endothelial tumor
Usually multicentric
Involves the skin and visceral organs
Very rarely involves the brain
May be caused by an enteric sexually transmitted agent
Associated with
Human Herpes Virus
8
Risk Factors
HIV Infection
AIDS
definining illness (less common with highly active
Retrovir
al therapy)
More common in those with oral or anal sexual contacts
Symptoms
Lesions typically non-pruritic
Initial: Painless
Later: Lesions may become painful as they enlarge
Signs
Cutaneous lesions
Pigmented (violaceous)
Red-blue/purple or bluish-brown
Plaque
s,
Papule
s and
Nodule
s
Flush with skin or raised strawberry-like
Plaque
s
Lesions enlarge, coalesce and may bleed
Can involve any area of the skin
Especially common on the soles of the feet
Rarely affects the palms of the hands
Signs
Intraoral disease
Intraoral disease present at time of diagnosis: 50%
Higher risk of gastrointestinal involvement
Signs
Gastrointestinal involvement (Usually asymptomatic)
Dysphagia
Gastric outlet obstruction
Gallbladder
Signs
Pulmonary involvement
Rapidly fatal if not treated
Usually symptomatic
Non-productive cough
Bronchospasm
Dyspnea
Pleural Effusion
in 20-50% cases at diagnosis
Pleural Fluid
negative for Kaposi's Sarcoma
Transudative or exudative
Chest XRay
Reticulonodular
Pulmonary Infiltrate
s
Much coarser than with
Pneumocystis carinii
Normal gallium scan
Bronchoscopy
Characteristic endobronchial lesions
Biopsy usually avoided secondary to bleeding
Labs
Biopsy
Histology Findings
Dermis
with increased spindle cells and vascularization
Significant plasma cell infiltration
Histology differentiates from
Bacillary Angiomatosis
Cutaneous
Cryptococcus
Differential Diagnosis
Dermatofibroma
Bacillary Angiomatosis
Hemosiderotic
Hemangioma
Fibrous histiocytoma
Interstitial
Granuloma Annulare
Arteriovenous Malformation
Pyogenic Granuloma
Management
Gene
ral
Evaluate for underlying predisposing condition (esp.
HIV Infection
)
No treatment is curative!
Slow the progression of systemic disease
Manage local or regional problems
Management
Medications
Chemotherapy
Cytotoxic drugs (Indicated for widespread disease)
Doxorubicin
Vinblastine
Vincristine
Bleomycin
Interferon
alpha
Better with Less extensive cutaneous lesions
Better if no edema or visceral disease
Radiation Therapy
Control
Lymphedema
Control painful or necrotic bulky tumors
Surgical Resection
Indicated for local complications
Cryotherapy
or
Liquid Nitrogen
Indicated to ablate single lesions
Resources
Kaposi Sarcoma (Orphanet)
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=33276
Kaposi Sarcoma (Stat Pearls)
https://www.ncbi.nlm.nih.gov/books/NBK534839/
References
Helm (2023) Am Fam Physician 107(2): 191-2 [PubMed]
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