de Lima Maria Helena N, Harshbarger Raymond J, George Timothy M
Dell Children's Medical Center of Central Texas, Austin, Tex., USA.
Pediatr Neurosurg. 2013;49(3):187-92. doi: 10.1159/000358924. Epub 2014 Apr 3.
Slit ventricle syndrome (SVS) is a known late complication of shunting procedures. Some patients develop cephalocranial disproportion (CCD) that will require surgical treatment to increase craniocerebral compliance.
We performed cranial vault distraction osteogenesis to treat 2 teenage patients who presented with SVS, increased intracranial pressure and CCD. Bilateral temporo-parieto-occipital craniotomies were performed.
Both patients successfully completed distraction and consolidated without the need for bone grafting. Postoperatively, both patients showed an increase in intracranial and intraventricular volume, as well as decreased shunt revisions. One patient had improvement of her headaches, while the other continues to have chronic headaches.
Distraction osteogenesis is an option to expand the cranial vault in older children with SVS and CCD, in which the traditional cranial vault expansion would be a challenge and may or may not provide adequate expansion.
裂隙脑室综合征(SVS)是分流手术已知的晚期并发症。一些患者会出现头颅比例失调(CCD),这需要手术治疗以增加颅腔顺应性。
我们采用颅骨牵引成骨术治疗2例患有SVS、颅内压升高和CCD的青少年患者。实施了双侧颞顶枕开颅手术。
两名患者均成功完成牵引并愈合,无需植骨。术后,两名患者的颅内和脑室内体积均增加,分流修正次数减少。一名患者的头痛症状有所改善,而另一名患者仍有慢性头痛。
牵引成骨术是扩大患有SVS和CCD的大龄儿童颅腔的一种选择,在这种情况下,传统的颅腔扩大术将是一项挑战,且可能无法提供足够的扩大效果。