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伴有幕下延伸的幕上囊性血管母细胞瘤——独特的位置及罕见的婴儿病例

Supratentorial cystic hemangioblastoma with infratentorial extension--a unique location and a rare infant case.

作者信息

Tekkök Ismail H, Sav Aydin

机构信息

MESA Hospital/Neurosurgery, 06510 Ankara, Turkey.

出版信息

Childs Nerv Syst. 2006 Sep;22(9):1177-81. doi: 10.1007/s00381-006-0052-4. Epub 2006 Mar 14.

DOI:10.1007/s00381-006-0052-4
PMID:16534645
Abstract

INTRODUCTION

Supratentorial occurrence of hemangioblastoma is an exceedingly rare event. Even rarer is the occurrence of a supratentorial hemangioblastoma in infancy.

CASE REPORT

We hereby report the case of an 18-month-old girl who presented with irritability, increasing head size, and an open fontanelle. MR scans demonstrated triventricular hydrocephalus and a cystic mass within the left lateral ventricle. There was an 18 x 15 x 13 mm enhancing nodule along the medial aspect of the cyst. The cystic mass was mainly supratentorial but there was a caudal extension through the tentorial incisura that compressed the cerebellum. At surgery, the content of the cyst was xanthochromic. Enhancing medial nodule was extremely vascular and was extirpated totally. The pathological diagnosis was reticular variant of hemangioblastoma.

CONCLUSION

The child is well at 4 years of age. An extensive review of the English literature revealed only three such cases. All three cases survived the operation.

摘要

引言

幕上血管母细胞瘤的发生极为罕见。而婴儿期幕上血管母细胞瘤的发生则更为罕见。

病例报告

我们在此报告一名18个月大女童的病例,该女童表现为易激惹、头围增大及囟门未闭。磁共振成像扫描显示三脑室积水及左侧脑室内有一囊性肿块。沿囊肿内侧缘有一个18×15×13毫米的强化结节。囊性肿块主要位于幕上,但有一个尾状延伸穿过小脑幕切迹并压迫小脑。手术中,囊肿内容物呈黄色。强化的内侧结节血管极为丰富,已被完全切除。病理诊断为血管母细胞瘤的网状变异型。

结论

该患儿4岁时情况良好。对英文文献的广泛检索仅发现3例此类病例。所有3例均手术存活。

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Hemangioblastomas of the central nervous system in von Hippel-Lindau syndrome and sporadic disease.冯·希佩尔-林道综合征及散发性疾病中的中枢神经系统血管母细胞瘤
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Intracranial neoplasms in the first year of life: results of a second cohort of patients from a single institution.一岁以内儿童的颅内肿瘤:来自单一机构的第二批患者的研究结果
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