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[室管膜囊肿——病例报告]

[Ependymal cyst--case report].

作者信息

Morimoto T, Kaneko M, Nishikawa R, Ono T, Basugi N

出版信息

No Shinkei Geka. 1986 Mar;14(3 Suppl):351-6.

PMID:3703134
Abstract

An eleven-month-old male infant with an ependymal cyst is reported. He was born after full-term pregnancy and vacuum extraction. His growth and development was somewhat retarded and he could control his head at the age of five months. He was admitted to our hospital because of the enlargement of his head and the paretic right upper limb. On admission he was found to be a well-nourished infant with the head circumference of 54.5 cm and the height of 75.5 cm. Physical examination disclosed slight weakness in the right upper extremity but no signs of increased intracranial pressure. Computed tomography (CT) revealed a huge low density area in the left frontoparietooccipital region which extended to the right across the midline. Another low density area was seen in the quadrigeminal cistern. CT findings also suggested an association with agenesis of the corpus callosum. The huge supratentorial cyst was isolated from the ventricles and subarachnoid space, which was shown by administration of metrizamide into the cyst. Carotid angiograms showed displacement of both anterior cerebral arteries to the right, which were dissociated from each other. This fact and an association with agenesis of the corpus callosum supported the idea that the cyst originiated in the interhemispheric fissure and expanded into both hemispheres. Cyst fluid was watery clear and protein and sugar contents were 13 mg/dl and 56 mg/dl respectively. The patient underwent a left frontal craniotomy and partial removal of the cyst wall was performed to make a communication with the ventricle. His postoperative course was uneventful and the weakness of the right upper extremity gradually improved.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

报告了一名患有室管膜囊肿的11个月大男婴。他足月妊娠后经真空吸引分娩。其生长发育有所迟缓,5个月时能控制头部。因头部增大和右上肢麻痹入住我院。入院时发现他是一名营养良好的婴儿,头围54.5厘米,身高75.5厘米。体格检查发现右上肢轻度无力,但无颅内压升高迹象。计算机断层扫描(CT)显示左额顶枕区有一个巨大的低密度区,跨越中线延伸至右侧。在四叠体池可见另一个低密度区。CT结果还提示与胼胝体发育不全有关。通过向囊肿内注入甲泛葡胺显示,巨大的幕上囊肿与脑室和蛛网膜下腔隔离。颈动脉血管造影显示双侧大脑前动脉向右移位,且相互分离。这一事实以及与胼胝体发育不全的关联支持了囊肿起源于大脑半球间裂并扩展至双侧半球的观点。囊液清澈如水,蛋白质和糖含量分别为13毫克/分升和56毫克/分升。患者接受了左额开颅手术,部分切除囊肿壁以使其与脑室相通。术后过程顺利,右上肢无力逐渐改善。(摘要截短至250字)

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[Ependymal cyst--case report].[室管膜囊肿——病例报告]
No Shinkei Geka. 1986 Mar;14(3 Suppl):351-6.

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