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Cranial migration of complete ventriculo-peritoneal shunt assembly.

机译:完整的脑室-腹膜分流器组件的颅骨迁移。

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摘要

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.
机译:一名10个月大的男童由于输水管狭窄而患有严重的先天性脑积水,并出现了整个脑室-腹膜(VP)分流器的颅骨迁移。完整的分流器组件,包括分流腔,已在扩张的心室中标出。迁移的分流器留在原地。在另一侧执行VP分流。 VP分流器的完全脑室内迁移是一种罕见的并发症。可以通过将连接器部位牢固地固定在骨膜上,以及避免较大的毛刺孔和硬脑膜开口来避免这种并发症。讨论了此类事件的可能机制以及相关文献。

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