Ebrahimzadeh Kaveh, Mirahmadi Eraghi Mohammad, Bidari Zerehpoosh Farahnaz, Tavasol Hesameddin Hoseini, Abbaszdeh Mahkameh, Dmytriw Adam A, Jahanshahi Fatemeh
Skull Base Research Center, Loghman-e Hakim Hospital, Shahid Beheshti University of Medical Sciences, Makhsoos St, South Karegar Ave, Tehran, 1333635445, Iran.
Student Research Committee, School of Medicine, Qeshm International Branch, Islamic Azad University, Qeshm, Iran.
J Med Case Rep. 2024 Dec 18;18(1):600. doi: 10.1186/s13256-024-04947-9.
Ganglioneuroma represents an uncommon benign tumor arising from the sympathetic nerves, and its development from the fifth nerve is an infrequent entity. Few ganglioneuromas arising from the fifth nerve have been discussed in literature. The authors describe the second pediatric ganglioneuroma arising from the fifth nerve.
A 7 year-old Asian male suffering from left-sided facial paresthesia, accompanied by several episodes of complex seizures over the past 2 years, presented to our clinic. The patient also complained of sudden unconsciousness and concurrent upward gaze lasting less than a minute. A brain computed tomography scan and magnetic resonance imaging revealed an isodense lesion containing focal calcifications measuring 31 × 28 mm and a solid mass extending from the pontine surface to Meckel's cave, probably originating from the fifth nerve or its root entry zone. The lesion was mildly hypointense on T1-weighted sequences and hyperintense on T2-weighted and fluid attenuated inversion recovery sequences. Gadolinium injection revealed only minimal heterogeneous enhancement. Histopathologic and immunohistochemical findings were consistent with ganglioneuroma. A lateral approach via retrosigmoid incision and suboccipital lateral craniectomy toward the cerebellopontine angle was performed under neuromonitoring supervision, and the postoperative period was uneventful.
Although ganglioneuroma arising from the fifth nerve is an extremely rare entity, it should be considered when diagnosing lesions in Meckel's cave or the cerebellopontine angle cistern.
神经节细胞瘤是一种罕见的起源于交感神经的良性肿瘤,起源于第五神经的情况更为罕见。文献中很少讨论起源于第五神经的神经节细胞瘤。作者描述了第二例起源于第五神经的儿童神经节细胞瘤。
一名7岁亚洲男性因左侧面部感觉异常就诊,过去2年伴有数次复杂发作。患者还主诉突然意识丧失及同时向上凝视持续不到1分钟。脑部计算机断层扫描和磁共振成像显示一个等密度病变,有局灶性钙化,大小为31×28毫米,还有一个实性肿块从脑桥表面延伸至梅克尔腔,可能起源于第五神经或其神经根入区。该病变在T1加权序列上呈轻度低信号,在T2加权和液体衰减反转恢复序列上呈高信号。钆增强扫描仅显示轻微不均匀强化。组织病理学和免疫组化结果与神经节细胞瘤一致。在神经监测下,通过乙状窦后切口和枕下外侧颅骨切除术向桥小脑角进行外侧入路手术,术后恢复顺利。
尽管起源于第五神经的神经节细胞瘤极为罕见,但在诊断梅克尔腔或桥小脑角池病变时应予以考虑。