Kaposi Sarcoma Flashcards

1
Q

Has what cell origin

A

Endothelial cell origin

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2
Q

linked w what type of infection?

A

HHV8

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3
Q

4 clinical variants

A

Classic KS, endemic African KS, immunosuppressive therapy-related KS,
HIV/AIDS-related KS.

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4
Q

systemic involvement

A

GI and lungs

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5
Q

African endemic type KS has what age prediliction and gender

A

young adults, mean age 35;
young children, mean age 3 years.

Males > females

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6
Q

what type of KS ,

Most common in solid transplant recipients as well as individuals treated chronically with immunosuppressive drugs. arises 16.5 months average after transplantation

A

Iatrogenic immunosuppression type

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7
Q

Risk of KS in HIV people compared w the general individual

A

Risk of KS 20,000 times that of the general population,

300 times that of other immunosuppressed individuals

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8
Q

Skin lesions.

A

most often starts as an ecchymotic-like macule
.Macules evolve into patches, papules, plaques, nodules, and tumors that
are violaceous, red, pink, or tan and become purple-brownish with a greening hemosiderin halo as they age. Often oval initially,and on the trunk enarranged parallel to skin tension lines . lesions may initially occur at sites of trauma, acral areas.

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9
Q

Distribution

A

almost always occur on the feet and legs or the hands, and slowly spread centripetally.

In HIV/AIDS-associated KS,there is early involvement to the face and widespread distribution on the trunk

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10
Q

Skin biopsy

A

Vascular channels lined by atypical endothelial cells among a network of reticulin fibers and extravasated erythrocytes with hemosiderin deposition.
In the nodular stage: Spindle cells in sheets and fascicles with mild- to-moderate cytologic atypia, single cell necrosis, trapped RBCs within an extensive network of slit like vascular spaces

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11
Q

Confirmation of dx is done by?

A

lesional skin biopsy

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12
Q

life span

A

CLASSIC KS Average survival,10to15years;
death usually from unrelated causes. Secondary malignancies arise in > 35% of cases.

AFRICAN-ENDEMIC KS Mean survival in young adults, 5 to 8 years; young children, 2 to
3 years.

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13
Q

tx

A

RADIOTHERAPY Indicated or tumorous lesions, conf uent lesions with a large sur ace area, large lesions on distal extremity, and large oropha- ryngeallesions.Cryosurgery.Indicated or deeply pigmented, protruding nodules. Laser Surgery. Pulsed-dye laser e ective or small super cial lesions. Photodynamic T erapy. For small super cial lesions.
ELECTROSURGERY E ective or ulcerated, bleeding nodular lesions. Excisional Surgery. E ective or selected small lesions. Intral- esional Cytotoxic Chemotherapy. Vinblastine, Vincristine,andBleomycin.
Aggressive Intervention
Single-Agent Chemotherapy. With adria- mycin, vinblastine, lipid ormulations o daunorubicin and doxorubicin. Paclitaxel
( axol), thalidomide, and col-3. Combination Chemotherapy. Vincristine + bleomycin + adriamycin or inter eron-α + zidovudine

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