Abstract
Kaposi’s sarcoma (KS) is a multifocal tumor of endothelial cell origin associated with human herpesvirus 8 (HHV-8) infection. Four epidemiological and clinical variants are described: (1) classic KS, (2) endemic African KS, (3) KS in therapeutically immunosuppressed patients, and (4) acquired immunodeficiency syndrome (AIDS)-associated KS. The diagnosis of KS is based on the clinical picture and laboratory investigations (histopathology, serological immune tests). Treatment for KS with localized skin lesions includes surgical excision, local destruction (liquid nitrogen, laser, photodynamic therapy, etc.), and radiotherapy. For patients with aggressive disease, the recommendations include liposomal anthracyclines or alternatively different types of mono- or combination chemotherapies including vinblastine or doxorubicin, bleomycin, vincristine, etoposide, and dacarbazine. In AIDS-associated KS in addition, highly active antiretroviral therapies (HAART) need to be initiated. In advanced, nonresponsive KS, the HAART regimen is supplemented with paclitaxel. In organ transplant patients, the immunosuppressive therapy needs reevaluation – a switch to rapamycin has been shown to result in regression of KS. Despite the implication of HHV-8 in KS pathogenesis, anti-herpetic drugs have no effect in KS treatment.
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Tschachler, E., Tiplica, GS. (2015). Kaposi’s Sarcoma. In: Katsambas, A.D., Lotti, T.M., Dessinioti, C., D’Erme, A.M. (eds) European Handbook of Dermatological Treatments. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-45139-7_46
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DOI: https://doi.org/10.1007/978-3-662-45139-7_46
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