Al Fauzi Asra, Djatisoesanto Wahjoe, Wahyuhadi Joni, Parenrengi Muhammad Arifin, Turchan Agus
Department of Neurosurgery, Universitas Airlangga, Dr. Soetomo General Hospital, Surabaya Neuroscience Institute, Surabaya, Indonesia.
Department of Urology, Universitas Airlangga, Dr. Soetomo General Hospital, Surabaya Neuroscience Institute, Surabaya, Indonesia.
J Pediatr Neurosci. 2017 Jan-Mar;12(1):96-98. doi: 10.4103/jpn.JPN_189_16.
Bladder migration and transurethral extrusion is an extremely rare complication of ventriculoperitoneal (VP) shunt. Only eight cases have been reported in the English literature since 1995. We report a case of a 4-year-old boy with cerebral palsy, hydrocephalus, and VP shunted on both sides who presented with a protruded distal VP shunt from his urethral orifice. The patient was reported for having previous shunt extrusion through the anus. The patient was treated on by a multidisciplinary approach, involving a neurosurgeon and urologist. Shunt removal with simple procedure was smoothly achieved without morbidities. He was discharged home in satisfactory condition.
膀胱迁移和经尿道挤出是脑室腹腔(VP)分流术极为罕见的并发症。自1995年以来,英文文献中仅报道过8例。我们报告一例4岁脑瘫、脑积水男孩,双侧均行VP分流术,其尿道外口有突出的VP分流管远端。据报道该患者既往曾有分流管经肛门挤出。患者接受了多学科联合治疗,涉及神经外科医生和泌尿外科医生。通过简单手术顺利移除分流管,未出现并发症。他出院时情况良好。