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围产期非典型畸胎样/横纹肌样瘤累及耳部深部结构并伴有动脉梗死。

Perinatal atypical teratoid/rhabdoid tumor involving the deep ear structures and complicated by arterial infarction.

作者信息

Alharbi Omar Abdullah, Almushayqih Musab Hamoud, Alqahtani Abdulmalik, Alsuhaibani Mohanned Saleh

机构信息

Department of Radiology, King Faisal Specialist Hospital and Research center, Riyadh, Saudi Arabia.

Department of Pathology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

出版信息

Radiol Case Rep. 2020 Sep 24;15(11):2433-2439. doi: 10.1016/j.radcr.2020.08.060. eCollection 2020 Nov.

Abstract

Atypical teratoid/rhabdoid tumor is a malignant pediatric brain tumor. Unusual invasive behavior of the dura and bony involvement of the deep ear structures and rapid progression in size complicated by arterial infarction have not been described before. A newborn girl presented with increased intracranial pressure. Medical imaging revealed a large mass centered in the left cerebellopontine angle and left middle cranial fossa with large supra-tentorial components associated with destruction of the left petrous bone with involvement of the inner and middle ear structures. Shortly, the tumor rapidly progressed in size and complicated by left middle cerebral artery territory infarction. The patient passed away after a short hospital course. This case report illustrates how rapid and aggressive the natural history of atypical teratoid/thabdoid tumor can be with unusual skull base destruction and deep ear structures involvement.

摘要

非典型畸胎样/横纹肌样瘤是一种小儿恶性脑肿瘤。硬脑膜异常浸润行为以及深部耳部结构的骨质受累,且肿瘤大小迅速进展并伴有动脉梗死,此前尚未见报道。一名新生女婴出现颅内压升高。医学影像显示,一个大肿块位于左小脑脑桥角和左中颅窝中心,幕上有较大部分,伴有左侧岩骨破坏,累及内耳和中耳结构。不久后,肿瘤大小迅速进展,并伴有左大脑中动脉供血区梗死。患者在住院病程较短后死亡。本病例报告说明了非典型畸胎样/横纹肌样瘤的自然病程可能有多迅速和侵袭性,伴有不寻常的颅底破坏和深部耳部结构受累。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e190/7519276/b447e428bb71/gr1.jpg

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