2002PubMedRequires access

[Panniculitis-like lymphoma clinically manifesting as alopecia].

László Török, Pálfi Tímea Gurbity, Ágnes Kirschner, László Krenács

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Abstract

A 45-year-old female patient discussed herein had a multifocal, alopecia areata of inflammatory character. Histological findings first suggested histiocyte cytophagic panniculitis, although a "burned-out" panniculitis-like T-cell lymphoma could not be excluded. After a two-year follow-up period assessment of the T-cell receptor gene rearrangement verified the diagnosis of subcutaneous panniculitis-like T-cell lymphoma. This case is interesting because of its isolated manifestation and a long-standing, benign course of the disease.

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What this paper is about

A 45-year-old female patient discussed herein had a multifocal, alopecia areata of inflammatory character. Histological findings first suggested histiocyte cytophagic panniculitis, although a "burned-out" panniculitis-like T-cell lymphoma could not be excluded. After a two-year follow-up period assessment of the T-cell receptor gene rearrangement verified the diagnosis of subcutaneous panniculitis-like T-cell lymphoma. This case is interesting because of its isolated manifestation and a long-standing, benign course of the disease.

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Available abstract

A 45-year-old female patient discussed herein had a multifocal, alopecia areata of inflammatory character. Histological findings first suggested histiocyte cytophagic panniculitis, although a "burned-out" panniculitis-like T-cell lymphoma could not be excluded. After a two-year follow-up period assessment of the T-cell receptor gene rearrangement verified the diagnosis of subcutaneous panniculitis-like T-cell lymphoma. This case is interesting because of its isolated manifestation and a long-standing, benign course of the disease.

Key concepts: Panniculitis, Medicine, Lymphoma, Cutaneous lymphoma, Pathology, Histiocyte, Dermatology, Mycosis fungoides

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