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一例伴有里德-施特恩伯格样细胞的恶性组织细胞增多症尸检病例。

An autopsy case of malignant histiocytosis with Reed-Sternberg-like cells.

作者信息

Nakanuma Y, Kurumaya H, Kurashima K

机构信息

Second Department of Pathology, Kanazawa University School of Medicine, Japan.

出版信息

Acta Pathol Jpn. 1989 Jan;39(1):79-83. doi: 10.1111/j.1440-1827.1989.tb02406.x.

Abstract

We report an autopsy case of malignant histiocytosis. The clinical course was rapidly progressive and terminated with jaundice and respiratory failure. Histologically, there was diffuse infiltration of large atypical cells in the liver, spleen, lymph nodes and bone marrow. It was of interest that these tumor cells contained a number of bizarre multinucleated cells histologically indistinguishable from Reed-Sternberg cells of Hodgkin's disease, and that these atypical cells expressed DAKO M1 (identical to Leu M1) and Ki-1 antigens and also showed binding to peanut agglutinin (PNA), representative markers of Reed-Sternberg cell. An absence of epithelial membrane antigen and presence of Leu M1 antigen in the tumor cells made a diagnosis of Ki-1 lymphoma unlikely. This case study showed that giant or pleomorphic cells indistinguishable histologically and phenotypically from Reed-Sternberg cells occur in malignant histiocytosis.

摘要

我们报告一例恶性组织细胞增多症的尸检病例。临床病程进展迅速,最终因黄疸和呼吸衰竭死亡。组织学检查显示,肝脏、脾脏、淋巴结和骨髓中有大量非典型细胞弥漫浸润。有趣的是,这些肿瘤细胞包含许多形态怪异的多核细胞,在组织学上与霍奇金病的里德-斯腾伯格细胞无法区分,并且这些非典型细胞表达DAKO M1(等同于Leu M1)和Ki-1抗原,还显示与花生凝集素(PNA)结合,这是里德-斯腾伯格细胞的代表性标志物。肿瘤细胞中上皮膜抗原缺失以及Leu M1抗原的存在使得Ki-1淋巴瘤的诊断不太可能。该病例研究表明,在恶性组织细胞增多症中会出现组织学和表型上与里德-斯腾伯格细胞无法区分的巨大或多形性细胞。

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