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一名髓母细胞瘤患儿后颅窝手术后出现钆增强的肥厚性橄榄体变性。

Hypertrophic olivary degeneration with gadolinium enhancement after posterior fossa surgery in a child with medulloblastoma.

作者信息

Nowak Johannes, Alkonyi Balint, Rutkowski Stefan, Homola György A, Warmuth-Metz Monika

出版信息

Childs Nerv Syst. 2014 May;30(5):959-62. doi: 10.1007/s00381-013-2296-0.

Abstract

Hypertrophic olivary degeneration (HOD) is a rare transsynaptic form of degeneration occurring secondary to the disruption of the dentato-rubro-olivary pathway ("Guillain-Mollaret triangle"). HOD can be caused by ischemic, hemorrhagic, traumatic, or neoplastic lesions, and it can also occur following posterior fossa surgery. MRI characteristics of HOD include T2 signal increase and hypertrophy. To date, blood–brain barrier disruption has not been reported in HOD. Here, we present the first case of HOD with temporary gadolinium enhancement in a 10-year-old child 7 months after resection of a posterior fossa medulloblastoma. The recognition of gadolinium enhancement as a radiological feature of HOD may help to distinguish between this benign secondary condition and tumor recurrence.

摘要

肥大性橄榄核变性(HOD)是一种罕见的跨突触性变性形式,继发于齿状核-红核-橄榄核通路(“ Guillain-Mollaret三角”)中断。HOD可由缺血性、出血性、创伤性或肿瘤性病变引起,也可在后颅窝手术后发生。HOD的MRI特征包括T2信号增强和肥大。迄今为止,尚未有关于HOD血脑屏障破坏的报道。在此,我们报告首例10岁儿童在后颅窝髓母细胞瘤切除术后7个月出现暂时性钆增强的HOD病例。认识到钆增强作为HOD的影像学特征可能有助于区分这种良性继发性疾病和肿瘤复发。

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