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顶枕叶孤立性朗格汉斯细胞组织细胞增生症病变:一例报告并文献复习

Solitary Langerhans cell histiocytosis lesion of the parieto-occipital lobe: a case report and review of the literature.

作者信息

Bergmann M, Yuan Y, Brück W, Palm K V, Rohkamm R

机构信息

Institute of Clinical Neuropathology, Zentralkrankenhaus Bremen-Ost, Germany.

出版信息

Clin Neurol Neurosurg. 1997 Feb;99(1):50-5. doi: 10.1016/s0303-8467(96)00586-0.

Abstract

A 38 year-old woman with a solitary intracerebral Langerhans cell histocytosis (LCH) lesion is presented, in whom, cerebral magnetic resonance imaging (MRI) revealed a non-enhancing mass in the right parieto-occipital lobe. The surgical specimen consisted of a nodular polymorphic infiltrate of mononuclear histiocytic cells, macrophages, eosinophilic granulocytes, lymphocytes and Langerhans giant cells involving leptomeninges, cerebral cortex and white matter. The histiocytes displayed features of Langerhans cells such as CD1a and S-100 immunopositivity, and of reticulum cells such as Ki-M4P and X-12 immunopositivity. This case as well as ten other cases from the literature are reviewed.

摘要

本文报告了一名38岁患有孤立性脑内朗格汉斯细胞组织细胞增多症(LCH)病变的女性,其脑部磁共振成像(MRI)显示右侧顶枕叶有一个无强化肿块。手术标本由单核组织细胞、巨噬细胞、嗜酸性粒细胞、淋巴细胞和朗格汉斯巨细胞组成的结节状多形性浸润灶,累及软脑膜、大脑皮层和白质。组织细胞表现出朗格汉斯细胞的特征,如CD1a和S-100免疫阳性,以及网状细胞的特征,如Ki-M4P和X-12免疫阳性。本文对该病例以及文献中的其他10例病例进行了综述。

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