Avula Shivaram, Kumar Ram, Pizer Barry, Pettorini Benedetta, Abernethy Laurence, Garlick Deborah, Mallucci Conor
Department of Radiology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK (S.A., L.A., D.G.); Department of Neurology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK (R.K.); Department of Oncology, Alder Hey Children's NHS Foundation Trust, Liverpool, UK (Barry Pizer); Department of Neurosurgery, Alder Hey Children's N.H.S Foundation Trust, Liverpool, UK (Benedetta Pettorini, C.M.).
Neuro Oncol. 2015 Apr;17(4):614-22. doi: 10.1093/neuonc/nou299. Epub 2014 Oct 15.
Posterior fossa syndrome (PFS) is an important complication of posterior fossa surgery in children. The pathophysiology of this condition remains unclear, but there is evidence implicating surgical injury of the proximal efferent cerebellar pathway (pECP) and the cerebellar vermis to PFS. We aimed to evaluate if diffusion abnormalities involving these structures on the final intraoperative MRI can predict the development of PFS.
Diffusion-weighted imaging from 31 posterior fossa resections were anonymized and evaluated for abnormalities involving the dentate nucleus, superior cerebellar peduncle, and the mesencephalic tegmentum forming the pECP, vermis, and middle cerebellar peduncle. The case notes were independently evaluated for evidence of PFS.
The diffusion imaging in 28 cases was of optimal quality for evaluation. Diffusion abnormalities were identified in 10 cases, 7 of which involved the pECP. Retrospective evaluation revealed evidence of PFS in 6 cases. There was a significant association between abnormalities involving pECP structures (P = .001) and development of PFS. Bilateral involvement of pECP (P = .006) was a highly specific risk factor for predicting the development of PFS. Diffusion abnormality of the inferior vermis was significantly associated with PFS (P = .001) but may not represent a risk factor in isolation.
This study demonstrates the feasibility of identifying children at risk for developing PFS at the earliest stage post tumor resection and thus adds to the growing evidence base on its pathophysiology.
后颅窝综合征(PFS)是儿童后颅窝手术的一种重要并发症。这种病症的病理生理学仍不清楚,但有证据表明,小脑传出近端通路(pECP)和小脑蚓部的手术损伤与PFS有关。我们旨在评估术中最后阶段的磁共振成像(MRI)上涉及这些结构的扩散异常是否能预测PFS的发生。
对31例后颅窝切除术的扩散加权成像进行匿名处理,并评估是否存在涉及齿状核、小脑上脚以及构成pECP、蚓部和小脑中脚的中脑被盖的异常情况。对病例记录进行独立评估,以寻找PFS的证据。
28例病例的扩散成像质量达到最佳评估标准。10例发现有扩散异常,其中7例涉及pECP。回顾性评估发现6例有PFS的证据。涉及pECP结构的异常与PFS的发生之间存在显著关联(P = 0.001)。pECP的双侧受累(P = 0.006)是预测PFS发生的一个高度特异性危险因素。小脑下蚓部的扩散异常与PFS显著相关(P = 0.001),但单独来看可能并不代表危险因素。
本研究证明了在肿瘤切除后的最早阶段识别有发生PFS风险儿童的可行性,从而为其病理生理学的证据基础增添了内容。