Suppr超能文献

[1例表现为小脑幕肿块性病变的硬脑膜型组织细胞增多症X]

[A case of dural type of histiocytosis X presenting as a mass lesion in the tentorium cerebelli].

作者信息

Baba T, Ibayashi Y, Morimoto S, Niwa J, Tanabe S, Hashi K

机构信息

Department of Neurosurgery, Sapporo Medical University School of Medicine.

出版信息

No Shinkei Geka. 1994 May;22(5):471-6.

PMID:8196835
Abstract

Histiocytosis X is a disease of unknown etiology, characterized by a mass of proliferating histiocytes, plasma cells and inflammatory cells foaming a granuloma within the reticuloendothelial elements of any organ in the body. In the central nervous system (CNS), hypothalamic disorder of histiocytosis X is often found, but histiocytosis X in other regions is quite rare. We report a case of a 5-year-old girl with histiocytosis X of the zygoma presenting as a mass lesion in the tentorium cerebelli. A computed tomographic (CT) scan demonstrated a tumor at the left tentorial region, extending along the dura mater of the tentorium cerebelli. Magnetic resonance imaging (MRI) revealed a low signal intensity region on both T1 and T2-weighted images. MRI with Gd-DTPA showed a homogeneous enhanced mass extending to right and inferior sites with a thickened tentorium. As the thickened dura matter continued from the left middle fossa to the mass lesion, the tumor was considered to arise from the left zygoma and extend to the tentorium cerebelli. CNS extension of histiocytosis X is manifested either as (1) the cerebral type or (2) the dural type. Many cases of cerebral type histiocytosis X including hypothalamic disorder have been reported. Only 6 cases of the dural type of histiocytosis X have been described. Although the lesions of the cerebral type of histiocytosis X show prolonged T1 and T2 values on MRI, the MRI findings of the dural type have not been reported. The present case is the first report of the appearance of the lesion on MRI.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

组织细胞增多症X是一种病因不明的疾病,其特征是大量增殖的组织细胞、浆细胞和炎性细胞在体内任何器官的网状内皮组织内形成肉芽肿。在中枢神经系统(CNS)中,常发现下丘脑组织细胞增多症X,但其他区域的组织细胞增多症X相当罕见。我们报告一例5岁女孩,患有颧骨组织细胞增多症X,表现为小脑幕上的肿块病变。计算机断层扫描(CT)显示左侧小脑幕区域有一个肿瘤,沿小脑幕硬脑膜延伸。磁共振成像(MRI)显示在T1和T2加权图像上均为低信号强度区域。使用钆喷酸葡胺(Gd-DTPA)的MRI显示一个均匀强化的肿块延伸至右侧和下方部位,小脑幕增厚。由于增厚的硬脑膜从左中颅窝延续至肿块病变,肿瘤被认为起源于左侧颧骨并延伸至小脑幕。组织细胞增多症X的中枢神经系统扩展表现为(1)脑型或(2)硬脑膜型。已经报道了许多包括下丘脑疾病在内的脑型组织细胞增多症X病例。仅描述了6例硬脑膜型组织细胞增多症X。尽管脑型组织细胞增多症X的病变在MRI上显示T1和T2值延长,但硬脑膜型的MRI表现尚未见报道。本病例是关于该病变在MRI上表现的首次报告。(摘要截断于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验