Licht Anna-K, Schulmeyer Frank, Allert Max, Held Paul, Woenckhaus Matthias, Strutz Jürgen
Department of Otorhinolaryngology, University of Regensburg, Regensburg, Germany.
Otol Neurotol. 2004 Mar;25(2):174-7. doi: 10.1097/00129492-200403000-00016.
To describe vertigo and hearing disturbance as a first sign of glioblastoma.
Case report.
Ear, Nose, and Throat Department of the University of Regensberg, Germany. Primary Care Center.
A patient with a left temporal glioblastoma.
A 67-year-old man presented with a 2-month history of vertigo and hearing disturbance. Radiological imaging revealed a left temporal tumor with dural inflation and erosion of the petrous bone and superior semicircular duct. The surgery involved total resection of the tumor and resurfacing of the gap in the superior canal. The histopathological examination revealed World Health Trade Organization IV glioblastoma. Postoperatively, the debilitating symptoms were relieved and the patient received radiation therapy. Tumor progression indicated a recraniotomy and a mastoidectomy. The tumor was only partially resected, and required chemotherapy. It subsequently developed otoliquorrhea and required a remastoidectomy. Histopathology of a pathological fracture of the X thoracic vertebra revealed a metastasis of the known glioblastoma. The patient died from respiratory distress syndrome.
To the best of our knowledge, we are presenting the first case with transdural infiltration of bony structures by a glioblastoma at the moment of diagnosis. The transdural spread could be via the sinus petrosus and along the nervous petrosus major in the petrosal bone. Superior canal dehiscence syndrome should be considered in the differential diagnosis of vertigo and hearing disturbance. Two different processes for the etiology of the superior canal dehiscence syndrome are discussed previously in the literature; however, we present a new entity with a tumor-cause dehiscence of the bone overlying the superior canal.
描述眩晕和听力障碍作为胶质母细胞瘤的首发症状。
病例报告。
德国雷根斯堡大学耳鼻喉科。初级保健中心。
一名左颞叶胶质母细胞瘤患者。
一名67岁男性出现2个月的眩晕和听力障碍病史。影像学检查显示左颞叶肿瘤,伴有硬脑膜膨隆及岩骨和上半规管侵蚀。手术包括肿瘤全切及对上半规管缺损处进行修复。组织病理学检查显示为世界卫生组织IV级胶质母细胞瘤。术后,致残症状缓解,患者接受了放射治疗。肿瘤进展后进行了再次开颅手术和乳突切除术。肿瘤仅部分切除,需要化疗。随后出现耳漏,需要再次进行乳突切除术。胸椎X线病理性骨折的组织病理学检查显示为已知胶质母细胞瘤转移。患者死于呼吸窘迫综合征。
据我们所知,我们报告的是首例在诊断时胶质母细胞瘤经硬脑膜浸润骨结构的病例。硬脑膜扩散可能通过岩窦并沿岩骨内的岩大神经进行。在眩晕和听力障碍的鉴别诊断中应考虑上半规管裂综合征。文献中先前已讨论过上半规管裂综合征病因的两种不同过程;然而,我们提出了一种新的情况,即上半规管上方骨质因肿瘤导致裂开。