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局限性眼眶神经纤维瘤

Localized orbital neurofibromas.

作者信息

Krohel G B, Rosenberg P N, Wright J E, Smith R S

出版信息

Am J Ophthalmol. 1985 Sep 15;100(3):458-64. doi: 10.1016/0002-9394(85)90514-8.

Abstract

Of nine patients (five men and four women, 25 to 55 years old) with localized orbital neurofibromas, only one had other systemic findings consistent with neurofibromatosis. The neurofibromas originated from sensory nerves of the orbit, producing gradual proptosis with expansion of the orbital walls in most cases. Mild orbital discomfort occurred in some patients. Preoperative and postoperative anesthesia in the distribution of the involved sensory nerves was also encountered. Five patients had multiple tumors within the same orbit. Four patients had tumors or a pedicle of the tumor extending into the superior orbital fissure. Two patients were initially thought to have fibrotic pseudotumors. Surgical excision is the treatment of choice for these tumors.

摘要

在9例患有局限性眼眶神经纤维瘤的患者(5名男性和4名女性,年龄在25至55岁之间)中,只有1例有其他与神经纤维瘤病相符的全身表现。这些神经纤维瘤起源于眼眶的感觉神经,多数情况下会随着眼眶壁的扩张而逐渐导致眼球突出。一些患者出现轻度眼眶不适。还遇到了受累感觉神经分布区域的术前和术后麻醉情况。5例患者在同一眼眶内有多个肿瘤。4例患者的肿瘤或肿瘤蒂延伸至眶上裂。2例患者最初被认为患有纤维化假瘤。手术切除是这些肿瘤的首选治疗方法。

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