Nadkarni Trimurti D, Menon Ram K, Dange Nitin N, Desai Ketan I, Goel Atul
Department of Neurosurgery, King Edward Memorial Hospital, Seth G.S. Medical College, Parel, Mumbai 400 012, India.
J Clin Neurosci. 2007 Jan;14(1):92-4. doi: 10.1016/j.jocn.2005.12.027. Epub 2006 Aug 28.
A 10-month-old male child with severe congenital hydrocephalus due to aqueduct stenosis presented with cranial migration of the entire ventriculo-peritoneal (VP) shunt. The complete shunt assembly, including the shunt chamber, was noted in the dilated ventricles. The migrated shunt was left in situ. A VP shunt was performed on the opposite side. The complete intraventricular migration of a VP shunt is a rare complication. This complication may be avoided by firm anchoring of the connector sites to the periosteum, and avoidance of large burr holes and dural openings. The possible mechanisms of such an event and the relevant literature are discussed.
一名10个月大的男性儿童因中脑导水管狭窄患有严重先天性脑积水,出现整个脑室-腹腔(VP)分流管向颅腔移位。在扩张的脑室内发现了完整的分流装置,包括分流腔。移位的分流管留在原位。在对侧进行了VP分流术。VP分流管完全移入脑室内是一种罕见的并发症。通过将连接部位牢固地固定在骨膜上,避免大的骨孔和硬脑膜开口,可以避免这种并发症。本文讨论了这一事件的可能机制及相关文献。