Komiyama M, Yasui T, Sakamoto H, Fujita K, Sato T, Ota M, Sugita M
Departments of Neurosurgery, Pediatric Neurosurgery, Pediatrics, Internal Medicine, Ophthalmology and Otorhinolaryngology, Osaka City General Hospital, Osaka, Japan.
Pediatr Neurosurg. 2000 Aug;33(2):100-4. doi: 10.1159/000028984.
Basal meningoencephalocele is frequently associated with midfacial anomaly, optic disc anomaly, brain anomaly, cerebrospinal fluid rhinorrhea, chiasma syndrome, and endocrinologic disturbance. The combination of basal meningoencephalocele and moyamoya disease is extremely rare. A 29-year-old man had basal meningoencephalocele (transsphenoidal type), anomaly of the optic disc (morning glory syndrome), panhypopituitarism and moyamoya disease. The patient was treated by hormone replacement, but surgical intervention was not required. Basal meningoencephalocele and moyamoya disease are a possible combination of the diseases.
基底型脑膨出常与面中部畸形、视盘异常、脑畸形、脑脊液鼻漏、视交叉综合征及内分泌紊乱相关。基底型脑膨出与烟雾病的组合极为罕见。一名29岁男性患有基底型脑膨出(经蝶型)、视盘异常(牵牛花综合征)、全垂体功能减退及烟雾病。该患者接受了激素替代治疗,但无需手术干预。基底型脑膨出和烟雾病是可能并存的疾病组合。