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Year : 1995  |  Volume : 61  |  Issue : 2  |  Page : 99--101

Sezary syndrome in a young woman

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
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Source of Support: None, Conflict of Interest: None

PMID: 20952903

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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).


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Online since 15th March '04
Published by Wolters Kluwer - Medknow