Alfieri Alessandra, Schettino Raffaele, Taborelli Angelo, Pontiggia Maurizio, Reganati Paolo, Ballarini Valerio, Monolo Luigi
Department of Neurosurgery, "A. Manzoni" Hospital, Lecco, Italy.
J Neurosurg. 2002 Nov;97(5):1212-6. doi: 10.3171/jns.2002.97.5.1212.
Temporosphenoidal encephaloceles are rare entities that occur when the temporal lobe herniates into the sphenoid sinus through a skull base defect of the temporal bone. Both an iatrogenic and a traumatic pathogenesis have been proposed. The authors describe a spontaneously occurring temporosphenoidal encephalocele in a 63-year-old woman who had a 4-year history of rhinorrhea. Spiral computerized tomography (CT) scanning revealed a bone defect located inside the ophthalmomaxillary triangle. The intrasphenoidal encephalocele had a heterogeneously hypointense signal compared with cerebrospinal fluid (CSF) on T1-weighted magnetic resonance (MR) images and a hyperintense signal compared with CSF on T2-weighted MR images. Two previous endonasal endoscopic procedures, performed by ear, nose, and throat surgeons, had been unsuccessful. The authors performed an endoscopic endonasal right nostril procedure by using 0 degrees and 45 degrees rigid-lens endoscopes that were 4 mm in diameter and 18 cm long. The encephalocele in the sphenoid sinus was partially removed. DuraGen and fat graft were positioned in the bone defect. Two No. 2 French detachable silicone balloons (1.5 cm3 volume) inflated with surgical glue were introduced into the skull defect and into the sphenoid sinus, respectively. The CSF leakage stopped immediately. No nasal packing or postoperative CSF lumbar drainage was necessary. The patient did well. Postoperative CT and MR imaging, obtained at 24 hours and at 3 months, demonstrated that the balloon and the fat graft filled the bone defect and the sphenoid sinus. Eight months postprocedure no CSF leakage was observed. This appears to be the first case reported in the literature of a temporosphenoidal encephalocele successfully treated by an endoscopic endonasal technique involving packing of the defect with inflated detachable balloons.
颞蝶部脑膨出是一种罕见的疾病,当颞叶通过颞骨的颅底缺损疝入蝶窦时发生。已提出医源性和创伤性两种发病机制。作者描述了一名63岁女性自发出现的颞蝶部脑膨出,该患者有4年的鼻漏病史。螺旋计算机断层扫描(CT)显示位于眶上颌三角内的骨缺损。蝶窦内的脑膨出在T1加权磁共振(MR)图像上与脑脊液(CSF)相比呈不均匀低信号,在T2加权MR图像上与CSF相比呈高信号。此前由耳鼻喉科医生进行的两次鼻内镜手术均未成功。作者使用直径4mm、长度18cm的0度和45度硬性透镜内镜进行了鼻内镜右鼻孔手术。蝶窦内的脑膨出被部分切除。将DuraGen和脂肪移植物放置在骨缺损处。分别将两个用手术胶水充气的2号法国可拆卸硅胶球囊(体积为1.5cm³)引入颅骨缺损处和蝶窦内。脑脊液漏立即停止。无需鼻腔填塞或术后脑脊液腰椎引流。患者情况良好。术后24小时和3个月进行的CT和MR成像显示,球囊和脂肪移植物填充了骨缺损和蝶窦。术后8个月未观察到脑脊液漏。这似乎是文献中报道的首例通过内镜鼻内技术成功治疗的颞蝶部脑膨出,该技术包括用充气的可拆卸球囊填充缺损。