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[儿童恶性组织细胞增多症]

[Malignant histiocytosis in children].

作者信息

Makhonova L A, Peterson I S, Zemskova V I, Pavlovskaia A I, Koposov P V

出版信息

Vopr Onkol. 1990;36(9):1063-7.

PMID:2238547
Abstract

The analysis of peculiarities of clinical course and morphology of malignant (acute) histiocytosis in 50 pediatric patients made a case for identification of the disease as separate pathology of histiocytic sarcoma type. Clinical course features include: lymphadenopathy, involvement of bones and--less frequently--lungs, skin and subcutaneous fat, marked fever and weight loss. Cytologic and histologic examination show polymorphic tumor cells of varying degree of differentiation, with blasts predominating. Well-developed Golgi complex, presence of lysosomes, phagosomes and erythrophagocytosis are among the characteristic ultrastructural features of the disease.

摘要

对50例儿科患者恶性(急性)组织细胞增多症的临床病程和形态学特征进行分析后,有理由将该疾病认定为组织细胞肉瘤类型的一种独立病理。临床病程特征包括:淋巴结病、骨骼受累,较少见的是肺部、皮肤和皮下脂肪受累、高热和体重减轻。细胞学和组织学检查显示不同分化程度的多形性肿瘤细胞,以原始细胞为主。发达的高尔基体、溶酶体、吞噬体的存在以及红细胞吞噬现象是该疾病的特征性超微结构特征。

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