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出血性腰骶部黏液乳头型室管膜瘤的非典型影像学表现及其与组织病理学的相关性:病例报告

Atypical Imaging of Hemorrhagic Lumbosacral Myxopapillary Ependymoma with Histopathological Correlation: A Case Report.

作者信息

Albadr Fahad, Albahkali Salha M, Alahmadi Mohammad S, Alsakkaf Hussein M, Al-Habib Amro, Alkhalidi Hisham, Basalamah Ali A

机构信息

Radiology Unit, King Saud University Medical City (KSUMC), College of Medicine, King Saud University, Riyadh, Saudi Arabia.

Department of Radiology, King Fahad Medical City (KFMC), Riyadh, Saudi Arabia.

出版信息

Am J Case Rep. 2020 Oct 21;21:e925449. doi: 10.12659/AJCR.925449.

Abstract

BACKGROUND Spinal myxopapillary ependymoma (MPE) is a slow-growing tumor arising from ependymal cells of the central nervous system. MPE rarely presents with acute neurological compromise and most commonly occur in the filum terminale or conus medullaris region. To date, only a few cases have been reported of patients presenting acutely because of hemorrhagic MPE. CASE REPORT A 16-year-old boy without previous medical problems presented with a sudden onset of severe pain in the low back radiating to the thighs. He could not walk owing to the severity of the pain. Neurological examination revealed an unsteady gait, but the rest of the motor and sensory examination was normal. Lumbosacral spine magnetic resonance imaging revealed an intradural hemorrhagic mass extending from L5 to S2. The encapsulated hemorrhagic tumor was resected, and the pathology was consistent with MPE grade I. The patient made a significant recovery postoperatively. It is extremely rare for MPE to present with spontaneous hemorrhage in the lumbosacral region. Prompt diagnosis and management led to a favorable outcome. This case report is intended to highlight the atypical presentation and imaging features of hemorrhagic MPE. CONCLUSIONS We described a rare case of MPE in the lumbosacral region of a patient who presented with acute neurological compromise and atypical imaging features.

摘要

背景 脊髓黏液乳头型室管膜瘤(MPE)是一种起源于中枢神经系统室管膜细胞的生长缓慢的肿瘤。MPE很少表现为急性神经功能损害,最常见于终丝或圆锥区域。迄今为止,仅有少数因出血性MPE而急性发病的病例报道。病例报告 一名16岁无前驱病史的男孩突然出现下腰部严重疼痛并放射至大腿。由于疼痛剧烈,他无法行走。神经学检查显示步态不稳,但其余运动和感觉检查正常。腰骶部脊柱磁共振成像显示硬膜内出血性肿块,从L5延伸至S2。切除了包膜完整的出血性肿瘤,病理结果符合I级MPE。患者术后恢复良好。MPE在腰骶部区域出现自发性出血极为罕见。及时的诊断和治疗带来了良好的结果。本病例报告旨在强调出血性MPE的非典型表现和影像学特征。结论 我们描述了一例腰骶部区域的罕见MPE病例,该患者表现为急性神经功能损害和非典型影像学特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a3/7588349/6c67946c66c6/amjcaserep-21-e925449-g001.jpg

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