Kurata H, Tamaki N, Sawa H, Oi S, Katayama K, Mochizuki M, Uetani Y, Yokoyama N, Nakamura H
Department of Neurosurgery, Kobe University School of Medicine, Japan.
Pediatr Neurosurg. 1996;24(1):52-4. doi: 10.1159/000121015.
The first known surviving case of acrania is presented. The patient was the first child of a 29-year-old Japanese woman. Fetal ventriculomegaly was documented in the 35th gestational week. Prenatal sonography and magnetic resonance imaging suggested hydrocephalus with a wide encephalomeningocele. The baby was born at 38 weeks of gestational age by vaginal delivery. The patient had no calvarium, but did have a complete skull base with a partial defect in the occipital scalp and an underlying dural defect. Subsequently, the patient underwent repair of the scalp defect. At 3 months of age, after hydrocephalus developed, a subduro-peritoneal shunt was placed because of cosmetic and nursing problems. His developmental quotient was 10 at 3 years.
首次报告已知存活的无脑儿病例。该患者是一名29岁日本女性的头胎。孕35周时记录到胎儿脑室扩大。产前超声和磁共振成像提示脑积水合并巨大脑膨出。婴儿在孕38周时经阴道分娩。患者无颅骨,但有完整的颅底,枕部头皮有部分缺损,硬脑膜有潜在缺损。随后,患者接受了头皮缺损修复术。3个月大时,出现脑积水后,因美观和护理问题置入了硬膜下-腹腔分流管。其3岁时发育商为10。