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孤立性三叉神经结节病肉芽肿酷似三叉神经鞘瘤:病例报告

Isolated trigeminal nerve sarcoid granuloma mimicking trigeminal schwannoma: case report.

作者信息

Quinones-Hinojosa Alfredo, Chang Edward F, Khan Saad A, McDermott Michael W

机构信息

Department of Neurosurgery, University of California at San Francisco, San Francisco, California 94143-0112, USA.

出版信息

Neurosurgery. 2003 Mar;52(3):700-5 discussion 704-5. doi: 10.1227/01.neu.0000048481.18726.aa.

Abstract

OBJECTIVE AND IMPORTANCE

Sarcoidosis most commonly presents as a systemic disorder. Infrequently, sarcoidosis can manifest itself in the central nervous system, with granulomas involving the leptomeninges and presenting with facial nerve weakness. Sarcoid of the trigeminal nerve is exceedingly rare and can mimic trigeminal schwannoma. We review the literature on sarcoid granulomas of the trigeminal nerve and compare their radiological features with the more common schwannoma.

CLINICAL PRESENTATION

A 33-year-old woman presented with a history of left-sided facial pain and numbness for 11 months, which was presumed to be trigeminal neuralgia. A trial of carbamazepine had been unsuccessful in relieving the facial pain. Her neurological examination revealed decreased facial sensation in the V(1)-V(2) distribution. Preoperative magnetic resonance imaging demonstrated a contrast-enhancing mass centered in the left cavernous sinus with extension along the cisternal portion of the left trigeminal nerve.

INTERVENTION

The patient underwent a left frontotemporal orbitozygomatic craniotomy with intraoperative neurophysiological monitoring of Cranial Nerves III, V, and VI and image guidance for subtotal microsurgical resection of what appeared, grossly and on frozen section, to be a neurofibroma. The final pathology report, however, revealed a sarcoid granuloma of the trigeminal nerve.

CONCLUSION

The differential diagnosis of contrast-enhancing lesions in the lateral wall of the cavernous sinus should include inflammatory conditions such as sarcoidosis. We recommend that surgery for biopsy or decompression be used only for those patients in whom a diagnosis cannot be confirmed with noninvasive testing. If surgery is performed, intraoperative frozen pathology is very useful in guiding the extent of resection.

摘要

目的及重要性

结节病最常表现为一种全身性疾病。结节病很少累及中枢神经系统,表现为软脑膜肉芽肿并伴有面神经麻痹。三叉神经结节病极为罕见,可类似三叉神经鞘瘤。我们回顾了关于三叉神经结节病肉芽肿的文献,并将其影像学特征与更常见的神经鞘瘤进行比较。

临床表现

一名33岁女性,有11个月左侧面部疼痛和麻木病史,曾被诊断为三叉神经痛。卡马西平试验未能缓解面部疼痛。神经系统检查显示V(1)-V(2)分布区面部感觉减退。术前磁共振成像显示一个强化肿块,位于左侧海绵窦,沿左侧三叉神经脑池段延伸。

干预措施

患者接受了左侧额颞眶颧开颅手术,术中对Ⅲ、Ⅴ、Ⅵ脑神经进行神经生理监测,并在影像引导下对大体及冰冻切片显示为神经纤维瘤的病变进行显微手术次全切除。然而,最终病理报告显示为三叉神经结节病肉芽肿。

结论

海绵窦外侧壁强化病变的鉴别诊断应包括结节病等炎症性疾病。我们建议,仅对那些无法通过无创检查确诊的患者进行活检或减压手术。如果进行手术,术中冰冻病理对指导切除范围非常有用。

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