Takase Hajime, Araki Kohta, Seki Shunsuke, Takase Kana, Murata Hidetoshi, Kawahara Nobutaka
Department of Neurosurgery, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Department of Neurosurgery, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
World Neurosurg. 2017 Feb;98:876.e1-876.e8. doi: 10.1016/j.wneu.2016.11.105. Epub 2016 Dec 1.
Intracranial carotid sympathetic plexus schwannoma (CSPS) is extremely rare; thus differential diagnostic criteria, optimal surgical strategies, and even a precise definition are lacking. Here we describe a case of CSPS and propose a definition and classification for previously reported cases.
A 54-year-old man presented with hypacusis and abducens nerve palsy. Radiologic examinations revealed a well-enhanced mass at the right medial temporal base with erosion of the petrous apex and intact perilesional cortical bone. Preoperative findings, such as spontaneous improvement of diplopia, absence of xerophthalmia or facial palsy, and laterally displaced internal carotid artery (ICA), suggested the atypical origins of the petrous apex schwannoma. The tumor was exposed using the subtemporal extradural approach and completely resected. Intact foramen ovale, rostrolateral displacement of the greater superficial petrosal nerve within the outer membrane of the tumor, eroded petrous apex and carotid canal, superolaterally displaced ICA, and lack of an obvious tumor attachment to any of the suspected nerves suggested that the tumor originated from the carotid sympathetic plexus of the petrous ICA. The patient fully recovered without neurological complications.
Preoperative diagnosis of petrous apex schwannoma is difficult: characteristic findings such as diplopia, hypacusis, and laterally displaced ICA may help. In addition, assessment of the relationship between the tumor and cavernous sinus could be useful in the determination of the surgical approach. Complete resection with good clinical outcome could be expected using Dolenc's approach (type A) and by the middle fossa extradural approach (type B) for intracavernous and extracavernous CSPS, respectively.
颅内颈动脉交感神经丛神经鞘瘤(CSPS)极为罕见;因此缺乏鉴别诊断标准、最佳手术策略,甚至缺乏精确的定义。在此,我们描述一例CSPS病例,并对先前报道的病例提出定义和分类。
一名54岁男性出现听力减退和展神经麻痹。影像学检查显示右侧颞叶内侧底部有一强化良好的肿块,岩尖骨质侵蚀,病变周围皮质骨完整。术前发现,如复视自发改善、无干眼症或面瘫,以及颈内动脉(ICA)向外移位,提示岩尖神经鞘瘤的非典型起源。采用颞下硬膜外入路暴露肿瘤并完全切除。卵圆孔完整,肿瘤外膜内岩浅大神经向 rostrolateral 移位,岩尖和颈动脉管侵蚀,ICA 向上外侧移位,且肿瘤与任何可疑神经均无明显附着,提示肿瘤起源于岩部 ICA 的颈动脉交感神经丛。患者完全康复,无神经并发症。
岩尖神经鞘瘤的术前诊断困难:复视、听力减退和 ICA 向外移位等特征性表现可能有所帮助。此外,评估肿瘤与海绵窦之间的关系可能有助于确定手术入路。对于海绵窦内和海绵窦外的 CSPS,分别采用 Dolenc 入路(A型)和中颅窝硬膜外入路(B型)有望实现完全切除并获得良好的临床效果。