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Case Reports
PMID: 20952903
Sezary syndrome in a young woman
Rajan T Damodaran, Sangeeta T Amladi, Hemangi R Jerajani
Department of Dermatology & Venereology, LTM Medical College, LTMG Hospital, Sion, Bombay - 400 022, India
Correspondence Address:
Rajan T Damodaran
F-1/13, Jumbo Darshan, Bombay - 400 069
India
Correspondence Address:
Rajan T Damodaran
F-1/13, Jumbo Darshan, Bombay - 400 069
India
| How to cite this article: Damodaran RT, Amladi ST, Jerajani HR. Sezary syndrome in a young woman. Indian J Dermatol Venereol Leprol 1995;61:99-101 |
Copyright: (C)1995 Indian Journal of Dermatology, Venereology, and Leprology
Abstract
A young female patient suffered for 4 months from a widespread erythroderma rash of unknown origin, marked by a peculiar hyperaesthesia. Haematological and biopsy findings were initially non-specific. A rapid deterioration, accompanied by infiltration of the skin, lymphadenopathy and hepatosplenomegaly was suggestive of Sézary syndrome, which was confirmed by finding of 40% of the lymphocytes being atypical (Sézary cells).
Keywords: Erythroderma, Sézary cells, Sézary syndrome
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