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双侧牵牛花综合征合并蝶骨脑膨出。病例报告。

Bilateral morning glory syndrome associated with sphenoid encephalocele. Case report.

作者信息

Itakura T, Miyamoto K, Uematsu Y, Hayashi S, Komai N

机构信息

Department of Neurological Surgery, Wakayama Medical College, Japan.

出版信息

J Neurosurg. 1992 Dec;77(6):949-51. doi: 10.3171/jns.1992.77.6.0949.

Abstract

Morning glory syndrome is a congenital anomaly of the optic disc in which the disc is enlarged and excavated, with white glial tissue in the center. A case is presented of morning glory syndrome associated with sphenoid encephalocele, median cleft lip, and agenesis of the corpus callosum. A 22-day-old boy was referred to the Wakayama Medical College Hospital for management of dyspnea due to a soft-tissue mass in the oral cavity. Magnetic resonance imaging revealed a mass extending through a bone defect in the sphenoid region and into the oral cavity. Surgical repair was attempted through a bifrontal craniotomy. A bone defect was identified in the sphenoid plate, through which the arachnoid membrane was connected to the oral cavity. Both optic nerves were elongated and adhered to the encephalocele. The wall of the meningocele was compressed digitally through the oral cavity and sutured to the dura mater of the bone defect. The operative findings suggest that a basal encephalocele protruding from a bone defect in the sphenoid plate may disturb the normal development of the optic nerve.

摘要

牵牛花综合征是一种视盘的先天性异常,表现为视盘扩大并凹陷,中央有白色神经胶质组织。本文报告一例牵牛花综合征合并蝶骨脑膨出、正中唇裂和胼胝体发育不全的病例。一名22日龄男婴因口腔软组织肿块导致呼吸困难被转诊至和歌山医科大学医院。磁共振成像显示一个肿块穿过蝶骨区域的骨缺损并延伸至口腔。尝试通过双额开颅手术进行修复。在蝶骨板上发现一个骨缺损,蛛网膜通过该缺损与口腔相连。双侧视神经拉长并附着于脑膨出。通过口腔用手指压迫脑膜膨出的壁并缝合至骨缺损的硬脑膜。手术结果表明,从蝶骨板骨缺损处突出的基底脑膨出可能会干扰视神经的正常发育。

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