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脑室腹腔分流术后儿童因巨大腹部脑脊液假性囊肿导致低钠血症性癫痫发作:一例报告

Hyponatremic seizure due to huge abdominal cerebrospinal fluid pseudocsyt in a child with ventriculoperitoneal shunt: a case report.

作者信息

Buyukyavuz Behcet Ilker, Duman Levent, Karaaslan Tamer, Turedi Aysen

机构信息

Suleyman Demirel University, Faculty of Medicine, Department of Pediatric Surgery, Isparta, Turkey.

出版信息

Turk Neurosurg. 2012;22(5):656-8. doi: 10.5137/1019-5149.JTN.3978-10.1.

Abstract

Placement of ventriculoperitoneal(VP) shunt is a worldwide accepted procedure for treatment of hydrocephalus. This procedure have various intra-abdominal complications, of which pseudocyst formation is a rare one. Common presentations of this complication are abdominal mass, abdominal pain, intestinal obstruction, and shunt dysfunction. In this paper, we report a case of 3 year-old boy with cerebrospinal fluid (CSF) pseudocyst of the VP shunt presenting with hyponatremic seizure. To the best of our knowledge, hyponatremic seizure has not been previously reported as a presentation of abdominal CSF pseudocyst in the literature. Our case has also the largest CSF pseudocyst with respect to body surface area of the child in the literature.

摘要

脑室腹腔(VP)分流术是治疗脑积水的一种全球公认的手术。该手术有多种腹腔内并发症,其中假性囊肿形成是一种罕见的并发症。这种并发症的常见表现为腹部肿块、腹痛、肠梗阻和分流功能障碍。在本文中,我们报告了一例3岁男孩,其VP分流术导致脑脊液(CSF)假性囊肿,并伴有低钠血症性癫痫发作。据我们所知,低钠血症性癫痫发作此前在文献中尚未被报道为腹部CSF假性囊肿的一种表现。就患儿体表面积而言,我们的病例也是文献中最大的CSF假性囊肿。

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