Akhaddar Ali, El-Mostarchid Brahim, Zrara Ibtissame, Boucetta Mohamed
Department of Neurosurgery, Mohamed V Military Hospital, Rabat, Morocco.
Neurosurgery. 2002 Mar;50(3):633-7; discussion 637-8. doi: 10.1097/00006123-200203000-00039.
Intracranial trigeminal neuroma extending extracranially is not a common finding. We report the case of a patient with a right cystic trigeminal neuroma arising in the middle temporal fossa and infratemporal areas. The clinical, radiological, and intraoperative features of these unusual lesions are discussed, and the relevant literature is reviewed.
A 35-year-old woman presented with a 4-year history of right serous otitis media associated with recent right facial paresthesia. A neurological examination revealed hypesthesia in the mandibular division of the right trigeminal nerve. Computed tomographic and magnetic resonance imaging scans demonstrated a 6 x 6 x 4-cm well-enhancing cystic mass arising from the middle temporal fossa and extending extracranially to the infratemporal fossa through the enlarged foramen ovale.
The tumor was extradural and originated from the right mandibular nerve. It was subtotally removed via a subtemporal-intradural and extradural approach. A pathological examination revealed a cystic neuroma. The patient has remained well during 12 months of follow-up, and no evidence of recurrence has been noted on magnetic resonance imaging studies.
Unilateral serous otitis media by obstruction of the eustachian tube is a rare initial manifestation of trigeminal neuroma. We emphasize the benefit of neuroradiological examinations (both computed tomographic scanning and magnetic resonance imaging), which provided the clearest preoperative localization of this large intra- and extracranial tumor. A combined frontotemporal and infratemporal fossa approach is preferred, considering the difficulty of surgical removal. The prognosis for most patients was good. Twenty-five previously reported cases were also reviewed.
颅内三叉神经瘤向颅外扩展并不常见。我们报告一例右侧囊性三叉神经瘤患者,肿瘤起源于颞中窝和颞下区域。讨论了这些不寻常病变的临床、影像学及术中特征,并复习相关文献。
一名35岁女性,有4年右侧浆液性中耳炎病史,近期出现右侧面部感觉异常。神经系统检查发现右侧三叉神经下颌支感觉减退。计算机断层扫描和磁共振成像扫描显示,一个6×6×4厘米大小、强化良好的囊性肿块,起源于颞中窝,通过扩大的卵圆孔向颅外延伸至颞下窝。
肿瘤位于硬膜外,起源于右侧下颌神经。通过颞下入路硬膜内和硬膜外联合手术,大部分切除肿瘤。病理检查显示为囊性神经瘤。患者在12个月的随访期间情况良好,磁共振成像检查未发现复发迹象。
咽鼓管阻塞导致的单侧浆液性中耳炎是三叉神经瘤罕见的首发表现。我们强调神经放射学检查(计算机断层扫描和磁共振成像)的益处,其能在术前最清晰地定位这个巨大的颅内及颅外肿瘤。考虑到手术切除的难度,首选额颞部和颞下窝联合入路。大多数患者预后良好。还复习了25例既往报道的病例。