Kaposi Sarcoma Flashcards

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1
Q

What is Kaposi Sarcoma (KS)?

A

A vascular tumor associated with infection by Human Herpesvirus-8 (HHV-8), characterized by proliferation of endothelial cells, inflammatory infiltrates, and angiogenesis.

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2
Q

What are the main types of Kaposi Sarcoma?

A

Classic KS: Occurs in elderly individuals, especially men of Mediterranean or Eastern European descent.

Endemic (African) KS: Seen in sub-Saharan Africa, not always associated with HIV.

Epidemic (AIDS-associated) KS: Linked to HIV/AIDS and immunosuppression.

Iatrogenic (Immunosuppressive therapy-associated) KS: Occurs in patients on immunosuppressive therapy, such as organ transplant recipients.

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3
Q

Which type of KS is most aggressive?

A

Epidemic (AIDS-associated) KS.

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4
Q

What virus is associated with Kaposi Sarcoma?

A

Human Herpesvirus-8 (HHV-8), also known as Kaposi Sarcoma-associated herpesvirus (KSHV).

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5
Q

How does HHV-8 contribute to the pathogenesis of KS?

A

HHV-8 infects endothelial cells, causing genetic alterations that promote proliferation and angiogenesis.

Viral proteins mimic cellular growth factors, enhancing tumor formation.

The immunosuppressed state (e.g., HIV) reduces control over HHV-8 replication.

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6
Q

What are the key factors that promote KS development?

A

Immunosuppression (e.g., HIV/AIDS, organ transplantation).

Chronic inflammation.

HHV-8 infection.

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7
Q

What are the characteristic skin lesions in Kaposi Sarcoma?

A

Red, purple, or brown macules, plaques, or nodules.

Lesions may be asymptomatic or tender and may ulcerate.

Often found on the lower extremities, face, oral cavity, or genitalia.

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8
Q

What is the pattern of lesion distribution in AIDS-associated KS?

A

Often widespread, involving the skin, mucous membranes, and internal organs.

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9
Q

What symptoms are seen with visceral involvement in KS?

A

Gastrointestinal (GI): Bleeding, obstruction, or diarrhea.

Pulmonary: Dyspnea, cough, hemoptysis, and pleural effusion.

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10
Q

How does endemic KS differ from classic KS?

A

Endemic KS may affect younger individuals and is more likely to involve lymph nodes and internal organs.

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11
Q

How is Kaposi Sarcoma diagnosed?

A

Clinical examination: Appearance and distribution of characteristic lesions.

Biopsy: Confirms diagnosis; histology shows spindle cells, slit-like vascular spaces, and extravasated red blood cells.

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12
Q

What is the role of immunohistochemistry in diagnosing KS?

A

Detection of HHV-8 latent nuclear antigen (LANA-1) confirms the presence of HHV-8.

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13
Q

What imaging studies are used for visceral involvement in KS?

A

Chest X-ray or CT: For pulmonary KS.

Endoscopy or colonoscopy: For gastrointestinal KS.

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14
Q

What is the cornerstone of treatment for AIDS-associated Kaposi Sarcoma?

A

Initiation or optimization of antiretroviral therapy (ART) to improve immune function.

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15
Q

What are the primary treatment options for localized KS lesions?

A

Cryotherapy or surgical excision.

Intralesional chemotherapy (e.g., vinblastine).

Radiation therapy for symptomatic or cosmetically concerning lesions.

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16
Q

What systemic therapies are used for widespread or aggressive KS?

A

Liposomal anthracyclines: Doxorubicin or daunorubicin.

Paclitaxel: For refractory or advanced cases.

17
Q

How is iatrogenic KS managed?

A

Reduction or cessation of immunosuppressive therapy if feasible.

18
Q

What factors influence the prognosis of Kaposi Sarcoma?

A

Immune status (CD4 count in AIDS-associated KS).

Extent of disease (localized vs. systemic).

Response to ART or systemic therapy.

19
Q

What are common complications of Kaposi Sarcoma?

A

Secondary infections in ulcerated lesions.

Bleeding from mucosal or GI lesions.

Airway or vascular obstruction in advanced cases.