Leukemic malignant histiocytosis.

M. Motoi, S. Moriwaki, H. Toki, K. Okabe, T. Yoshino, T. Akagi
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Abstract

Clinical, morphological, and ultrastructual studies are presented of three cases which had been diagnosed from lymph node biopsy as malignant histiocytosis. Three patients had a diffuse type of malignant histiocytosis and developed a leukemic phase at admission. Three patients survived for 1, 4 and 1 months after diagnosis. The neoplastic cells are characterized morphologically in the lymph nodes and in the peripheral blood by light microscopy and in two cases by electron microscopy also. These appear to be a spectrum of cell types in the leukemic malignant histiocytosis ranging from primitive reticulum cells or histiocytes to more differentiated monocytoid cells. No evidence for differentiation toward granulocytes was seen morphologically or immunohistochemically. The leukemic phase of malignant histiocytosis appears to be closely related to or identical histiocytic or monocytic leukemia (Schilling type) and should be differentiated from hairy cell leukemia. Necropsy findings from three cases are shortly reviewed.
白血病恶性组织细胞增多症。
本文报告三例淋巴结活检诊断为恶性组织细胞增多症的临床、形态学和超微结构研究。3例患者为弥漫性恶性组织细胞增多症,入院时发展为白血病期。3例患者诊断后分别存活1、4、1个月。在光镜和两例电子显微镜下,在淋巴结和外周血中有肿瘤细胞的形态学特征。这些似乎是白血病恶性组织细胞增多症的细胞类型谱,从原始网状细胞或组织细胞到分化程度更高的单核细胞。形态学或免疫组织化学未见向粒细胞分化的证据。恶性组织细胞增多症的白血病期似乎与组织细胞或单核细胞白血病(席林型)密切相关或相同,应与毛细胞白血病区分开来。本文将简要回顾三个病例的尸检结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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