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一例伴有自发性脾破裂的间变性淋巴瘤激酶阳性间变性大细胞淋巴瘤:一种极其罕见的表现。

A case of anaplastic lymphoma kinase-positive anaplastic large cell lymphoma presenting with spontaneous splenic rupture: an extremely unusual presentation.

作者信息

Hebeda K M, MacKenzie M A, van Krieken J H

机构信息

Department of Pathology, UMC St. Radboud, Nijmegen, The Netherlands.

出版信息

Virchows Arch. 2000 Oct;437(4):459-64. doi: 10.1007/s004280000251.

Abstract

In a 22-year-old male with a 10-day history of fever, painful swelling in the left groin, and abdominal complaints, emergency surgery was performed because of spontaneous splenic rupture. At histology, a cellular infiltrate of intermediate-sized atypical lymphocytes was seen in the splenic white pulp, staining for T-cell markers. In addition, CD30 and anaplastic lymphoma kinase 1 (ALK) were diffusely positive, thus, representing a case of anaplastic large cell lymphoma (ALCL), T-cell, ALK-positive, small cell monomorphic variant. ALK-positive ALCL patients generally bear a much better prognosis than patients with T-cell lymphomas, unspecified, or ALK-negative ALCL. Therefore, besides the very unusual clinical presentation, this case highlights the importance of immunostaining for CD30 and ALK in all T-cell lymphomas. This report is the first extensive description of ALK-positive ALCL involvement of the spleen.

摘要

一名22岁男性,有10天发热病史,左侧腹股沟疼痛性肿胀,伴有腹部不适,因自发性脾破裂接受了急诊手术。组织学检查显示,脾白髓中有中等大小非典型淋巴细胞的细胞浸润,对T细胞标志物染色阳性。此外,CD30和间变性淋巴瘤激酶1(ALK)弥漫性阳性,因此,这是一例间变性大细胞淋巴瘤(ALCL),T细胞型,ALK阳性,小细胞单形性变异型。ALK阳性的ALCL患者总体预后通常比未明确类型的T细胞淋巴瘤或ALK阴性的ALCL患者好得多。因此,除了非常不寻常的临床表现外,该病例还凸显了在所有T细胞淋巴瘤中对CD30和ALK进行免疫染色的重要性。本报告是对ALK阳性ALCL累及脾脏的首次详细描述。

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