Lymphangioma-like Kaposi’s sarcoma: Etiology and literature review
Identifieur interne : 00A632 ( Main/Exploration ); précédent : 00A631; suivant : 00A633Lymphangioma-like Kaposi’s sarcoma: Etiology and literature review
Auteurs : Daniel A. Davis [Royaume-Uni] ; Diane M. Scott [Royaume-Uni]Source :
- Journal of the American Academy of Dermatology [ 0190-9622 ] ; 2000.
Abstract
Much confusion surrounds a rare and occasionally described variant of Kaposi’s sarcoma (KS) known as lymphangioma-like or bullous KS. We describe the typical clinical and histologic features and elucidate the etiologic cell in lymphangioma-like KS. A computer-based review of the English-language literature was performed. Routine histologic and immunoperoxidase techniques were performed on formalin-fixed tissue. Immunoperoxidase staining for anti-CD31, anti-CD34, and anti-factor VIII–related antigen suggests that the etiologic cell of origin is the vascular endothelial cell. Lymphangioma-like KS has been described for more than a century and given various names. Dilated vascular spaces correlate with the clinically bullous lesions, which are veritable KS and not a secondary reaction to it. (J Am Acad Dermatol 2000;43: 123-7.)
Url:
DOI: 10.1067/mjd.2000.105564
Affiliations:
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