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皮肤血管免疫母细胞 T 细胞淋巴瘤的评估。

Evaluation of cutaneous angioimmunoblastic T-cell lymphoma.

机构信息

Washington University, Saint Louis, Missouri.

Washington University, Saint Louis, Missouri.

出版信息

J Am Acad Dermatol. 2011 Oct;65(4):855-862. doi: 10.1016/j.jaad.2010.05.030. Epub 2011 May 6.

Abstract

BACKGROUND

Angioimmunoblastic T-cell lymphoma (AITL) accounts for 18% of peripheral T-cell lymphomas worldwide. Skin involvement occurs in up to 50% of patients but poses a diagnostic dilemma because of the limited number of reported cases and subsequent lack of established diagnostic criteria.

OBJECTIVE

The purpose of this review is to examine common clinical, histologic, and molecular findings in cases of AITL with the hope of improving the diagnostic accuracy of this challenging condition.

METHODS

We present a case of AITL and conducted a review of the literature.

RESULTS

The common clinical and histologic features in cases of AITL are nonspecific. However, newer immunohistochemical stains and gene rearrangement studies appear very promising at improving diagnostic capabilities.

LIMITATIONS

There was a paucity of reported cases of AITL in the literature, and this review is retrospective.

CONCLUSION

AITL presents with nonspecific clinical and histologic findings, but immunohistochemical stains and gene rearrangements can help establish the diagnosis.

摘要

背景

血管免疫母细胞性 T 细胞淋巴瘤(AITL)占全球外周 T 细胞淋巴瘤的 18%。皮肤受累可达 50%,但由于报道病例数量有限,且缺乏既定的诊断标准,故存在诊断难题。

目的

本综述旨在探讨 AITL 中常见的临床、组织学和分子表现,以期提高对这一具有挑战性疾病的诊断准确性。

方法

我们呈现了 1 例 AITL 病例,并对文献进行了回顾。

结果

AITL 病例的常见临床和组织学特征不具特异性。然而,新型免疫组化染色和基因重排研究似乎在提高诊断能力方面非常有前景。

局限性

文献中 AITL 病例报道较少,本综述为回顾性研究。

结论

AITL 临床表现和组织学特征不具特异性,但免疫组化染色和基因重排有助于确立诊断。

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