术中在一名恰里畸形患者体内发现一个放射学上隐匿的阻塞膀胱出口的副膀胱瘤--一个罕见病例

Sophie F. Peeters, Lauren Uhr, Srinivas Chivukula, Richard Everson, Duc Duong, Duncan McBride, Won Kim, Marcia Cornford, Anton Mlikotic, Isaac Yang
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引用次数: 0

摘要

Chiari(I 型)畸形通常是先天性的。然而,扁桃体疝偶尔会继发于脑脊液漏、后窝或脑室内肿块病变或其他病因。我们报告了首例颈髓交界处的髓内椎体下吲哚瘤,伴有椎骨异常和获得性继发性Chiari畸形。术前影像学检查未发现肿块病变,但显示存在Chiari畸形。医生建议她进行后窝减压术,同时进行扁桃体缩小术。手术过程中,意外发现一个髓内肿块,阻塞了颈髓交界处的obex。切除病灶的组织病理学分析显示,诊断结果为脐下瘤。"由于脐下瘤在神经影像学中表现不明显,有时会给诊断带来困难。这种肿块与获得性Chiari畸形有关的情况很少见。此前还没有此类病例的报道。我们对获得性Chiari畸形进行了文献综述,并讨论了其治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intraoperative discovery of a radiographically occult subependymoma obstructing the obex in a patient with a Chiari malformation – A rare case
Chiari (type I) malformations are typically congenital. Occasionally, however, tonsillar herniation can arise secondary to cerebrospinal fluid leakage, posterior fossa or intraventricular mass lesions, or other etiologies. We present the first-ever case of an intramedullary subependymoma at the cervicomedullary junction associated with vertebral bone abnormalities and an acquired secondary Chiari malformation. A 60-year-old woman presented with a 3-year history of occipital, tussive headaches. Preoperative imaging was negative for mass lesions but demonstrated a Chiari malformation. She was recommended posterior fossa decompression with tonsillar shrinkage. During surgery, an intramedullary mass was incidentally observed, obstructing the obex at the cervicomedullary junction. Histopathological analysis of the resected lesion revealed a diagnosis of subependymoma. Subependymomas can sometimes present a diagnostic challenge due to their subtle appearance in neuroimaging. Only rarely are such masses associated with an acquired Chiari malformation. No such case has previously been reported. We present a literature review on acquired Chiari malformations and discuss their management.
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