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表现为急性阑尾炎的T细胞表型血管嗜性(血管内)大细胞淋巴瘤,见于一名获得性免疫缺陷综合征患者。

Angiotropic (intravascular) large cell lymphoma of T-cell phenotype presenting as acute appendicitis in a patient with acquired immunodeficiency syndrome.

作者信息

Malicki D M, Suh Y K, Fuller G N, Shin S S

机构信息

Department of Pathology, UCSD Medical Center, San Diego, Calif, USA.

出版信息

Arch Pathol Lab Med. 1999 Apr;123(4):335-7. doi: 10.5858/1999-123-0335-AILCLO.

Abstract

We describe a patient with acquired immunodeficiency syndrome who presented with acute appendicitis but was found to have angiotropic large cell lymphoma (ALCL) by pathologic examination of the appendectomy specimen, without acute inflammation. Very rare cases of angiotropic large cell lymphoma have been reported in patients with human immunodeficiency virus infection, and most cases of this rare lymphoma are of B-cell origin, but in this instance immunohistochemical analysis showed a T-cell phenotype.

摘要

我们描述了一名获得性免疫缺陷综合征患者,该患者表现为急性阑尾炎,但阑尾切除标本的病理检查发现为血管中心性大细胞淋巴瘤(ALCL),无急性炎症。在人类免疫缺陷病毒感染患者中已报告过非常罕见的血管中心性大细胞淋巴瘤病例,且这种罕见淋巴瘤的大多数病例起源于B细胞,但在此病例中,免疫组化分析显示为T细胞表型。

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