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一例罕见的小儿腰椎脊髓室管膜瘤误诊为脑膜炎的病例。

A Rare Case of Pediatric Lumbar Spinal Ependymoma Mimicking Meningitis.

作者信息

Ekuma Ezeali Mike, Ito Kiyoshi, Chiba Akihiro, Hara Yosuke, Kanaya Kohei, Horiuchi Tetsuyoshi, Ohaegbulam Samuel, Hongo Kazuhiro

机构信息

Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan; Memfys Hospital for Neurosurgery, Enugu, Nigeria.

Department of Neurosurgery, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

World Neurosurg. 2017 Apr;100:710.e1-710.e5. doi: 10.1016/j.wneu.2017.02.016. Epub 2017 Feb 13.

DOI:10.1016/j.wneu.2017.02.016
PMID:28216208
Abstract

Spontaneous acute subarachnoid hemorrhage (SAH) from lumbar ependymoma in children is rare. We report a case of a 14-year-old boy who developed sudden radicular low back pain while playing baseball. He was initially managed conservatively in a local hospital for suspected lumbar disc herniation, but he later developed meningeal symptoms and fever before being referred to our hospital. He underwent a diagnostic lumbar puncture in the emergency department; his cerebrospinal fluid suggested an SAH. Physical examination showed meningeal signs and cauda equina features. Cerebrospinal fluid analysis was negative for bacterial meningitis. Lumbar magnetic resonance imaging revealed a mass characterized as a hemorrhagic lesion. The patient had an emergent evacuation of the mass through the posterior approach. Postoperatively, his symptoms resolved completely. The histologic diagnosis was, surprisingly, an ependymoma (World Health Organization grade II). This case is particularly interesting because of its rarity in children, and its pattern of presentation. Although bacterial or viral meningitis is the most frequent cause of meningeal features in children, SAH from a hemorrhagic spinal tumor should be considered. Ultimately, a high index of suspicion is needed for prompt diagnosis.

摘要

儿童腰椎室管膜瘤导致的自发性急性蛛网膜下腔出血(SAH)较为罕见。我们报告一例14岁男孩,他在打棒球时突然出现放射性下腰痛。最初在当地医院因疑似腰椎间盘突出症接受保守治疗,但后来出现脑膜症状和发热,随后被转诊至我院。他在急诊科接受了诊断性腰椎穿刺;脑脊液提示为SAH。体格检查显示有脑膜刺激征和马尾神经症状。脑脊液分析排除了细菌性脑膜炎。腰椎磁共振成像显示一个以出血性病变为特征的肿块。患者通过后路紧急行肿块切除术。术后,他的症状完全缓解。令人惊讶的是,组织学诊断为室管膜瘤(世界卫生组织二级)。该病例因其在儿童中罕见以及其临床表现模式而特别有趣。虽然细菌性或病毒性脑膜炎是儿童脑膜症状最常见的原因,但应考虑出血性脊髓肿瘤导致的SAH。最终,需要高度怀疑指数以实现快速诊断。

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World Neurosurg. 2017 Apr;100:710.e1-710.e5. doi: 10.1016/j.wneu.2017.02.016. Epub 2017 Feb 13.
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