
Vol. 210, No. 4, 2005
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Case Report
Atypical Poorly Differentiated Cutaneous T-Cell Lymphoma with an Angiocentric Growth Pattern Presenting Histologically as Vasculitis
B. Laetsch, G. Hofbauer, W. Kempf, G. Burg, R. Dummer
Dermatologische Klinik, Universitätsspital Zürich, Zürich, Schweiz
Address of Corresponding Author
Dermatology 2005;210:341-345 (DOI: 10.1159/000084763)
Key Words
- Cutaneous T-cell lymphoma
- Angiocentric growth pattern
- Paraneoplastic vasculitis
Abstract
We report the case of a 41-year-old patient with an aggressive cutaneous T-cell lymphoma (CTCL) initially presenting on histology as lymphocytic vasculitis. On repeated histological examination and by molecular biology work-up, the diagnosis of an unclassifiable CTCL could eventually be established. This atypical poorly differentiated lymphoma was of a CD4+ CD8- CD56- phenotype and followed an unfavourable course. The patient died despite chemo- and immunotherapy 7 months after the first consideration of lymphoma as diagnosis. Copyright © 2005 S. Karger AG, Basel
Author Contacts
Prof. Reinhard Dummer Dermatologische Klinik, Universitätsspital Zürich Gloriastrasse 31 CH-8091 Zürich (Switzerland) Tel. +41 44 255 25 07, Fax +41 44 255 89 88, E-Mail reinhard.dummer@usz.ch
Article Information
Received: April 22, 2004
Accepted: September 24, 2004
Number of Print Pages : 5
Number of Figures : 5, Number of Tables : 0, Number of References : 28 |
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