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淋巴结间叶性网状细胞肉瘤

Lymph node interdigitating reticulum cell sarcoma.

作者信息

Chan W C, Zaatari G

出版信息

Am J Clin Pathol. 1986 Jun;85(6):739-44. doi: 10.1093/ajcp/85.6.739.

Abstract

A 67-year-old man presented with a malignant tumor involving abdominal lymph nodes, spleen, liver, and lungs, with associated protracted fever and night sweats. The tumor consisted of large pleomorphic cells, often surrounding microabscesses. Intracytoplasmic S100 protein, surface T6, Leu-3a (T4), and HLA-DR antigens were demonstrated. The malignant cells also possessed ATPase activity. Ultrastructurally, the cells exhibited numerous interdigitating cell processes but no Birbeck granules. The anatomic distribution of the tumor, its ultrastructural features, immunologic phenotype, and enzymatic profile are all consistent with a derivation from lymph node interdigitating reticulum cell. The tumor was unresponsive to the chemotherapeutic agents administered, and the patient soon died.

摘要

一名67岁男性患者,患有累及腹部淋巴结、脾脏、肝脏和肺部的恶性肿瘤,并伴有持续发热和盗汗。肿瘤由大的多形性细胞组成,常围绕微脓肿。细胞浆内可见S100蛋白、表面T6、Leu-3a(T4)和HLA-DR抗原。恶性细胞还具有ATP酶活性。超微结构显示,细胞有许多相互交错的细胞突起,但无伯贝克颗粒。肿瘤的解剖分布、超微结构特征、免疫表型和酶谱均符合淋巴结交错突网状细胞来源。该肿瘤对所用化疗药物无反应,患者很快死亡。

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