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[1例伴有脑干肿瘤的马富西综合征]

[A case of Maffucci's syndrome with brain-stem tumor].

作者信息

Sato K, Hayashi M, Katsumura H, Ishii H, Kubota T

机构信息

Department of Neurosurgery, Fukui Medical School, Japan.

出版信息

No To Shinkei. 1989 Jun;41(6):631-4.

PMID:2803830
Abstract

A case of Maffucci's syndrome with brain-stem tumor is reported. A 17-year-old man with a history of diplopia and unsteady gait for 5 months was admitted to our hospital on May 6, 1987. Neurological findings on admission disclosed left VIIth cranial nerve and bilateral VIIth nerve palsies and mild quadriplegia with a bilateral Babinski sign. His left limbs were deformed and disproportionally shortened since birth, and there were multiple enchondroma of the phalanges. Several bluish subcutaneous soft tumors were present on his left hand. Histological examination of a skin lesion confirmed the cavernous hemangioma. A CT scan showed diffuse symmetrical low density area in the brain-stem. No contrast enhancement was noted. Sagittal magnetic resonance imaging (MRI) demonstrated swelling of the brain stem especially in the pons and medulla oblongata. Left vertebral angiogram showed an avascular mass in the region brain stem. Brain-stem glioma being strongly suspected, both radiation therapy and chemotherapy were performed. After 66 Gy irradiation and ACNU administration, his neurological deficits gradually improved. The patient was discharged from the hospital on foot on August 7, 1987. The sagittal MRI taken on January 24, 1988 disclosed that the brain-stem swelling was apparently diminished. Maffucci's syndrome is a congenital, non-hereditary mesodermal dysplasia associated with multiple enchondromas and subcutaneous hemangioma. Although numerous tumors of the central nervous system have been described in association with Maffucci's syndrome, to our knowledge, no mention has been made of lesions in the brain-stem. The present case is an extremely rare instance of this syndrome complicated by the occurrence of a brain-stem tumor.

摘要

报告一例伴有脑干肿瘤的马富西综合征。一名17岁男性,有5个月复视和步态不稳病史,于1987年5月6日入院。入院时神经系统检查发现左侧第七颅神经及双侧第七神经麻痹,轻度四肢瘫,双侧巴宾斯基征阳性。自出生以来,其左上肢畸形且不成比例地缩短,指骨有多发内生软骨瘤。左手有几个蓝色皮下软组织肿瘤。皮肤病变的组织学检查证实为海绵状血管瘤。CT扫描显示脑干弥漫性对称低密度区,未见对比增强。矢状面磁共振成像(MRI)显示脑干肿胀,尤其是脑桥和延髓。左侧椎动脉血管造影显示脑干区域有一个无血管肿块。强烈怀疑为脑干胶质瘤,遂进行了放疗和化疗。在接受66 Gy照射及给予阿糖胞苷后,其神经功能缺损逐渐改善。患者于1987年8月7日步行出院。1988年1月24日的矢状面MRI显示脑干肿胀明显减轻。马富西综合征是一种先天性、非遗传性中胚层发育异常,与多发内生软骨瘤和皮下血管瘤有关。尽管已有许多中枢神经系统肿瘤与马富西综合征相关的报道,但据我们所知,尚无关于脑干病变的提及。本例是该综合征并发脑干肿瘤的极为罕见的病例。

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