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Primary cutaneous CD20-positive T-cell lymphoma.
Martin, Blanca; Stefanato, Catherine; Whittaker, Sean; Robson, Alistair.
Afiliação
  • Martin B; Department of Dermatopathology, St John's Institute of Dermatology, St Thomas Hospital, London, UK. blancamartin@hotmail.com
J Cutan Pathol ; 38(8): 663-9, 2011 Aug.
Article em En | MEDLINE | ID: mdl-21623866
ABSTRACT
CD20 is a transmembrane protein that is expressed by B cells during their development and is, therefore, commonly used to label cells of B lineage in lymphoid infiltrates. CD20-positive T-cell lymphoma is infrequent but well recognized. Cases reported in the literature show a variety of clinical and histoimmunochemical profiles. Primary cutaneous CD20-positive T-cell lymphoma is vanishingly rare; only eight cases have been previously reported. We present two new cases of this entity and describe their clinical, histological and immunohistochemical features. CD20 is a highly specific B-cell marker. However, it has been reported in a subset of normal T-cells in peripheral blood and bone marrow of healthy individuals. This subset of T-cells also expresses more often CD8 and g/d than the CD20-negative T-cells. Two main theories have been postulated to explain the expression of CD20 by neoplastic T-cells. The first possibility is that these lymphomas develop from the CD20-positive subset of normal T-cells. The second theory regards CD20 as an activation marker. Prognostic implications and therapeutic options of T-cell lymphomas with positivity for CD20 remain to be elucidated.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Linfoma Cutâneo de Células T / Antígenos CD20 Tipo de estudo: Prognostic_studies Limite: Aged80 / Humans / Male / Middle aged Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Linfoma Cutâneo de Células T / Antígenos CD20 Tipo de estudo: Prognostic_studies Limite: Aged80 / Humans / Male / Middle aged Idioma: En Ano de publicação: 2011 Tipo de documento: Article