Kawajiri K, Matsuoka Y, Hayazaki K
Department of Neurosurgery, Saiseikai Ibaraki Hospital, Osaka.
Neurol Med Chir (Tokyo). 1994 Jan;34(1):10-4. doi: 10.2176/nmc.34.10.
A 16-year-old male with cerebellar astrocytoma and a 29-year-old male with convexity meningioma, both complicated by hydrocephalus, developed pneumocephalus following tumor removal and shunt emplacement. Both patients underwent ventriculoperitoneal shunt emplacement and total tumor removal, and were discharged from hospital in good condition. After 1 year or 10 months, respectively, pneumocephalus and porencephalic cysts in the temporal lobes developed. Since neuroradiological examination could not locate the bone defects in the skull base, the dura mater covering the anterior cranial fossa was repaired. Fistulae were observed in the cribriform plate in both patients. Postoperatively, one patient showed persistent cerebrospinal fluid rhinorrhea. Intratympanic cerebrospinal fluid retention was demonstrated by tympanic puncture ipsilateral to a porencephalic cyst. The other patient again developed pneumocephalus. Magnetic resonance imaging indicated that the base of the porencephalic cyst was in contact with the tegmen tympani. The dura mater covering the floor of the middle cranial fossa was repaired in both patients, and the symptoms ameliorated. The bone defects in the skull base were apparently deeply involved in the development of the porencephalic cysts, indicating that such cysts provide useful information for locating cranial bone defects.
一名患有小脑星形细胞瘤的16岁男性和一名患有凸面脑膜瘤的29岁男性,均合并脑积水,在肿瘤切除和分流置入后发生了气颅。两名患者均接受了脑室腹腔分流置入和肿瘤全切术,并康复出院。分别在1年或10个月后,两名患者出现了气颅和颞叶脑穿通畸形囊肿。由于神经放射学检查无法定位颅底的骨缺损,故对覆盖前颅窝的硬脑膜进行了修复。两名患者的筛板均发现有瘘管。术后,一名患者出现持续性脑脊液鼻漏。通过对脑穿通畸形囊肿同侧进行鼓膜穿刺,证实存在鼓室内脑脊液潴留。另一名患者再次出现气颅。磁共振成像显示脑穿通畸形囊肿底部与鼓室盖接触。两名患者均对覆盖中颅窝底部的硬脑膜进行了修复,症状得到改善。颅底的骨缺损显然与脑穿通畸形囊肿的发生密切相关,表明此类囊肿为定位颅骨缺损提供了有用信息。