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冯雷克林霍增氏病中的听神经瘤

Acoustic neuroma in von Recklinghausen's disease.

作者信息

Per-Lee J H, Clairmont A A

出版信息

South Med J. 1976 Jul;69(7):844-7. doi: 10.1097/00007611-197607000-00009.

Abstract

Bilateral acoustic neuromas are common in von Recklinghausen's disease. Their surgical removal likely will produce total hearing loss unless the lesions are small and intracanalicular. Therefore, a posterior fossa myelogram is indicated in all patients when a diagnosis of neurofibromatosis is made. To preserve hearing in resection of small tumors, a middle fossa approach is appropriate. In lesions slightly larger than intracanalicular size, hearing may be preserved with a two-stage middle fossa and transsigmoid approach. The prospect of total hearing loss and even facial diplegia predisposes to surgical procrastination. However, the morbidity and mortality associated with removal of medium and large tumors may be greater for neurofibromatosis than for patients with singular acoustic neuromas. Therefore, we believe it is not advisable to postpone operation when tumors extend into the cerebral pontine angle, even though it means loss of hearing.

摘要

双侧听神经瘤在冯·雷克林霍增氏病中很常见。除非肿瘤较小且位于内听道内,否则手术切除很可能导致全聋。因此,一旦诊断为神经纤维瘤病,所有患者均需进行后颅窝脊髓造影。为了在切除小肿瘤时保留听力,中颅窝入路是合适的。对于略大于内听道大小的肿瘤,采用中颅窝和乙状窦后联合两阶段入路可能保留听力。全聋甚至双侧面瘫的可能性会导致手术拖延。然而,与单发听神经瘤患者相比,神经纤维瘤病患者切除中大型肿瘤的发病率和死亡率可能更高。因此,我们认为当肿瘤延伸至脑桥小脑角时,即使这意味着听力丧失,也不宜推迟手术。

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