Schroeder Henry W S, Oertel Joachim, Gaab Michael R
Department of Neurosurgery, Ernst Moritz Arndt University, Greifswald, Germany.
J Neurosurg. 2004 Aug;101(2):227-32. doi: 10.3171/jns.2004.101.2.0227.
Epidermoid tumors located in the cerebellopontine angle (CPA) are challenging lesions because they grow along the subarachnoid spaces around delicate neurovascular structures and often extend into the middle cranial fossa. The purpose of this study was to determine the value of endoscopic assistance in the microsurgical resection of these lesions, in which total removal is the therapy of choice.
Eight patients harboring an epidermoid tumor of the CPA were treated using an endoscope-assisted microsurgical technique. A retrosigmoid suboccipital approach was used in five patients and a pterional transsylvian approach was chosen in the other three. In four patients the lesion was resected microsurgically and the endoscope was used repeatedly to verify complete tumor removal, whereas most of the tumor mass was removed with the aid of an operating microscope in the other four. Tumor parts extending into other cranial compartments that were not visible through the microscope were removed under endoscopic view by using rigid rod-lens scopes with 30 and 70 degrees angles of view. All epidermoids were completely evacuated and the membranes were widely resected. Large tumors occupying both the middle and posterior cranial fossa were removed through a single small opening without enlarging the craniotomy. Permanent hearing loss and permanent hypacusis were observed in one patient each. One patient with facial and one with abducent nerve palsy recovered within 6 and 4 months, respectively. A transient weakness of the chewing muscles was encountered in one patient. Postoperative magnetic resonance imaging revealed no residual tumor in any patient. To date no recurrences have been-observed (follow up range 12-98 months).
The endoscope-assisted microsurgical technique enables safe removal even when tumor parts are not visible in a straight line. Tumor extensions into adjacent cranial compartments can be removed with the same approach without retracting neurovascular structures or enlarging the craniotomy.
位于桥小脑角(CPA)的表皮样肿瘤是具有挑战性的病变,因为它们沿着精细神经血管结构周围的蛛网膜下腔生长,并且常常延伸至中颅窝。本研究的目的是确定内镜辅助在这些病变显微手术切除中的价值,其中完全切除是首选治疗方法。
8例患有CPA表皮样肿瘤的患者采用内镜辅助显微手术技术进行治疗。5例患者采用乙状窦后枕下入路,另外3例选择翼点经侧裂入路。4例患者通过显微手术切除病变,反复使用内镜以确认肿瘤完全切除,而另外4例患者大部分肿瘤组织借助手术显微镜切除。通过使用30度和70度视角的硬性棒状透镜式内镜,在内镜视野下切除延伸至显微镜无法看到的其他颅腔的肿瘤部分。所有表皮样肿瘤均被完全清除,包膜被广泛切除。占据中颅窝和后颅窝的大型肿瘤通过单一小切口切除,无需扩大颅骨切开术。分别有1例患者出现永久性听力丧失和永久性听力减退。1例面神经麻痹患者和1例展神经麻痹患者分别在6个月和4个月内恢复。1例患者出现咀嚼肌短暂无力。术后磁共振成像显示所有患者均无肿瘤残留。迄今为止未观察到复发(随访范围12 - 98个月)。
内镜辅助显微手术技术即使在肿瘤部分无法直线可视时也能安全切除。肿瘤向相邻颅腔的延伸部分可采用相同方法切除,无需牵拉神经血管结构或扩大颅骨切开术。