Cutaneous and lymphadenopathic Kaposi’s sarcoma: a case report and review of literature
Article first published online: 5 FEB 2008
DOI: 10.1111/j.1600-0560.2007.00844.x
© Blackwell Munksgaard 2008
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How to Cite
Hussein, M. R. (2008), Cutaneous and lymphadenopathic Kaposi’s sarcoma: a case report and review of literature. Journal of Cutaneous Pathology, 35: 575–578. doi: 10.1111/j.1600-0560.2007.00844.x
Publication History
- Issue published online: 6 MAY 2008
- Article first published online: 5 FEB 2008
- Accepted for publication June 6, 2007
- Abstract
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Kaposi’s sarcoma (KS) of childhood is an extremely rare and unexplained disease. It is usually associated with immunosuppression and human herpes virus 8 (HHV-8) infection. It can involve skin, mucous membranes, lymph nodes and viscera. This investigation describes a case of a 3-year-old boy with cutaneous and lymphangiopathic KS. Initially, the patient presented with cutaneous lesions of KS behind the right ear. Two months later, the disease disseminated not only cutaneously but also to the cervical, axillary and inguinal lymph nodes. Immunological evaluation showed severe lymphocytopenia but without evidence of human immunodeficiency virus infection. The vascular nature of the lesion was supported by positive staining for CD31 and CD34. This study examines the clinicopathologic features of KS in children and summarizes the relevant literature.

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