| Literature DB >> 16008654 |
Brad Jones1, Yin Vun, Muna Sabah, Conleth A Egan.
Abstract
A 67-year-old man presented with a history of lymphadenopathy, fevers and separate skin eruptions of erythrodermic spongiotic dermatitis initially and subsequent toxic epidermal necrolysis. Initial lymph node biopsies showed non-specific granulomatous changes, and skin biopsies and bone marrow aspirate were not diagnostic. His toxic epidermal necrolysis responded well to 3 days of intravenous immunoglobulin. The patient was discharged from hospital and reviewed regularly as an outpatient. Due to persisting lymphadenopathy, further lymph node biopsy led to the diagnosis of angioimmunoblastic T-cell lymphoma, a rare form of peripheral T-cell lymphoma with a poor prognosis. At the time of diagnosis his condition deteriorated rapidly and he died soon after.Entities:
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Year: 2005 PMID: 16008654 DOI: 10.1111/j.1440-0960.2005.00177.x
Source DB: PubMed Journal: Australas J Dermatol ISSN: 0004-8380 Impact factor: 2.875