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鞍内海绵状血管瘤的多学科管理:病例报告及文献综述

Multidisciplinary management of an intra-sellar cavernous hemangioma: Case report and review of the literature.

作者信息

Chibbaro S, Cebula H, Ganau M, Gubian A, Todeschi J, Lhermitte B, Proust F, Noel G

机构信息

Neurosurgery Department, Strasbourg University Hospital, Strasbourg, France.

Neurosurgery Department, Strasbourg University Hospital, Strasbourg, France.

出版信息

J Clin Neurosci. 2018 Jun;52:135-138. doi: 10.1016/j.jocn.2018.03.021. Epub 2018 Apr 2.

Abstract

Extra-axial cavernous hemangiomas (ECH) are rare vascular lesions with a tendency to grow within the medial structures of the middle cranial fossa. This pathological entity lacks specific symptoms, and falls into the category of differential diagnosis of space occupying lesions in the cavernous sinus (CS) with or without sellar involvement, including those of tumoral, vascular and inflammatory nature. Of note, ECH can also be indolent, and is at times discovered incidentally during autopsy investigations. On radiological studies, ECH with sellar extension are frequently mistaken at first for pituitary adenomas. Total removal of intrasellar-CS ECH is technically demanding and burdened by remarkable morbidity and mortality rates, mostly related to the complex neuroanatomy of the CS-sellar region (i.e., peri and postoperative bleeding, and transitory or permanent nerve palsies, hormonal deficits). Consequently, only a few cases of successful total removal have been reported so far in the literature. Surgical debulking with cranial nerve decompression followed by stereotactic radiosurgery is currently considered the best alternative to total removal when the latter carries excessive perioperative risks. We present a rare case of a mainly located intrasellar ECH extending to the left CS discussing its clinical features and focusing on the most relevant aspects of the surgical management along with a review of the pertinent literature.

摘要

颅外海绵状血管瘤(ECH)是一种罕见的血管病变,倾向于在中颅窝内侧结构内生长。这种病理实体缺乏特异性症状,属于海绵窦(CS)占位性病变鉴别诊断的范畴,无论是否累及鞍区,包括肿瘤性、血管性和炎性病变。值得注意的是,ECH也可能进展缓慢,有时在尸检时偶然发现。在影像学研究中,累及鞍区的ECH最初常被误诊为垂体腺瘤。完全切除鞍内 - CS的ECH技术要求高,且并发症和死亡率显著,主要与CS - 鞍区复杂的神经解剖结构有关(即围手术期和术后出血,以及短暂或永久性神经麻痹、激素缺乏)。因此,迄今为止文献中仅报道了少数成功完全切除的病例。当完全切除带来过高的围手术期风险时,手术减瘤并进行颅神经减压,随后进行立体定向放射外科治疗目前被认为是最佳替代方案。我们报告一例罕见的主要位于鞍内的ECH延伸至左侧CS的病例,讨论其临床特征,并重点关注手术治疗的最相关方面,同时回顾相关文献。

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