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A primary cutaneous non-T, non-B CD4+, CD56+ lymphoma.

作者信息

Dummer R, Potoczna N, Häffner A C, Zimmermann D R, Gilardi S, Burg G

机构信息

Department of Dermatology, University of Zürich, Switzerland.

出版信息

Arch Dermatol. 1996 May;132(5):550-3.

PMID:8624152
Abstract

BACKGROUND

Cutaneous lymphomas are heterogeneous clonal lymphoproliferative disorders originating from B or T lymphocytes.

OBSERVATION

We describe a patient with a unique primary cutaneous lymphoma characterized by a bruise-like aspect of the skin lesions, a CD4+, CD43+, CD56+, CD2-, CD3-, CD8-, T-cell receptor-negative phenotype of the medium-sized to large lymphoid tumor cells and an undetermined genotype (T-cell receptor beta and immunoglobulin heavy chain in germline configuration, no clonal T-cell receptor gamma population as detected after analysis with polymerase chain reaction combined with denaturing gradient gel electrophoresis) and fast relapse after radiotherapy.

CONCLUSIONS

This non-B, non-T cutaneous lymphoma cannot be classified by any current lymphoma classification. It seems to represent a new disease entity with peculiar clinical, histologic, and molecular features.

摘要

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