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Telangiectatic Kaposi's Sarcoma: Occurrence in a Patient With Thymoma and Myasthenia Gravis Receiving Long-term Immunosuppresive Therapy

Authors :
Snyder, Robert A.
Schwartz, Robert Allen
Source :
Archives of Dermatology; December 1982, Vol. 118 Issue: 12 p1020-1021, 2p
Publication Year :
1982

Abstract

Kaposi's sarcoma is a distinctive malignant neoplasm of multifocal origin that most commonly affects the skin and gastrointestinal tract tissues.1-3 It classically presents as violaceous patches, plaques, or nodules that usually occur initially on the lower extremities.4 Less commonly, the disease first appears in other cutaneous or extracutaneous sites. This neoplasm has been given considerable attention in recent years because of its apparent association with immunosuppression. In this report, a patient who was chronically immunosuppressed had an unusual clinical variant of this disorder, which consisted of fleshcolored and erythematous telangiectatic papules and nodules. REPORT OF A CASE A 69-year-old man was hospitalized in November 1980 for the treatment of pneumonia. On admission, he was noted to have multiple flesh-colored nodules on the left lower extremity of uncertain duration. Myasthenia gravis had been diagnosed in 1963 and was initially treated with pyridostigmine bromide. In 1974, a Coombs'-positive hemolytic anemia

Details

Language :
English
ISSN :
0003987X and 15383652
Volume :
118
Issue :
12
Database :
Supplemental Index
Journal :
Archives of Dermatology
Publication Type :
Periodical
Accession number :
ejs28477530
Full Text :
https://doi.org/10.1001/archderm.1982.01650240064026