Kaposi sarcoma of the musculoskeletal system : A review of 66 patients
β Scribed by Gabriel Caponetti; Bruce J. Dezube; Carlos S. Restrepo; Liron Pantanowitz
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 420 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0008-543X
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β¦ Synopsis
Abstract
Kaposi sarcoma (KS) of bone and skeletal muscle is unusual. In this report, the authors review 66 published patients with KS who had involvement of the musculoskeletal system reported from 1925 to 2006. In only 3 patients was acquired immunodeficiency syndrome (AIDS)βrelated KS identified within skeletal muscle. Osseous KS lesions were more frequent and occurred with African, classic, and AIDSβrelated KS and occurred rarely in transplantationβassociated KS. Patients seldom were asymptomatic. They usually had bone pain with limited mobility or infrequently developed serious sequelae like spinal cord compression. Locally aggressive African and classic KS lesions typically involved the peripheral skeleton; whereas, in patients with AIDS, the axial (vertebrae, ribs, sternum, and pelvis) and/or maxillofacial bones more commonly were involved. Almost all patients had concomitant nonosseous KS lesions. Joint involvement was exceptional, and pathologic fractures were not observed. Computed tomography scans and magnetic resonance images were better at detecting osseous KS lesions, which frequently went undetected on plain xβray films or bone scans. Pathologic diagnosis was important to exclude similar lesions like bacillary angiomatosis. Treatment options, including surgery and, in more recent patients, radiation and/or chemotherapy, had limited success. Cancer 2007 Β© 2007 American Cancer Society.
π SIMILAR VOLUMES
Background. Not every patient with Kaposi's sarcoma (KS) has acquired immunodeficiency syndrome (AIDS). The "classic" form of KS is rare, and is associated with an indolent course. It is very distinct from AIDS-associated KS in which oral involvement is common and may be the initial presenting featu
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