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原发性皮肤爱泼斯坦-巴尔病毒相关T细胞淋巴增殖性疾病——2例临床病程异常且迁延的病例

Primary cutaneous Epstein-Barr virus-associated T-cell lymphoproliferative disorder-2 cases with unusual, prolonged clinical course.

作者信息

Park Sanghui, Lee Dong-Youn, Kim Won Seog, Ko Young-Hyeh

机构信息

Department of Pathology, Gil Medical Center, Gachon University, Incheon, Korea.

出版信息

Am J Dermatopathol. 2010 Dec;32(8):832-6. doi: 10.1097/DAD.0b013e3181d68381.

Abstract

Hydroa vacciniforme-like lymphoma and extranodal-type natural killer (NK)/T-cell lymphoma are prototypes of Epstein-Barr virus (EBV)-associated cutaneous T- or NK-cell lymphomas. Hydroa vacciniforme-like lymphoma with systemic spread and extranodal-type NK/T-cell lymphoma are characterized by aggressive clinical course. We describe 2 patients with primary cutaneous EBV-associated T-cell lymphomas who did not satisfy the criteria for well-defined entities and showed unusual, prolonged clinical course. They presented with skin ulcerations and mass lesions confined to the extremities without systemic involvement. Skin biopsies demonstrated dense superficial and deep perivascular and periappendageal lymphoid infiltrates expressing CD3 and CD8, but not CD56. The EBV genomes were found within the tumor cells, and monoclonal T-cell receptor gene rearrangement was present. We suggest that these cases represent a peculiar subtype of EBV+ cutaneous T-cell lymphoma, with a tendency to localize in the skin of the extremities and has an indolent clinical course.

摘要

种痘样水疱病样淋巴瘤和结外型自然杀伤(NK)/T细胞淋巴瘤是与爱泼斯坦-巴尔病毒(EBV)相关的皮肤T或NK细胞淋巴瘤的原型。伴有全身播散的种痘样水疱病样淋巴瘤和结外型NK/T细胞淋巴瘤具有侵袭性临床病程。我们描述了2例原发性皮肤EBV相关T细胞淋巴瘤患者,他们不符合明确实体的标准,且呈现出不寻常的、病程延长的情况。他们表现为局限于四肢的皮肤溃疡和肿块病变,无全身受累。皮肤活检显示密集的浅表和深部血管周围及附属器周围淋巴样浸润,表达CD3和CD8,但不表达CD56。在肿瘤细胞内发现了EBV基因组,且存在单克隆T细胞受体基因重排。我们认为这些病例代表了EBV阳性皮肤T细胞淋巴瘤的一种特殊亚型,倾向于定位于四肢皮肤,且临床病程呈惰性。

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