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一例原发性脊髓囊尾蚴病硬膜内髓外型被误诊为蛛网膜囊肿。

A case of intradural-extramedullary form of primary spinal cysticercosis misdiagnosed as an arachnoid cyst.

作者信息

Yoo Minwook, Lee Chang-Hyun, Kim Ki-Jeong, Kim Hyun-Jib

机构信息

Department of Neurosurgery, Spine Center, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

出版信息

J Korean Neurosurg Soc. 2014 Apr;55(4):226-9. doi: 10.3340/jkns.2014.55.4.226. Epub 2014 Apr 30.

Abstract

We describe a rare case of intradural-extramedullary primary spinal cysticercosis. A 42-year-old man visited our institute for lower back pain. He denied having consumed raw meet. Magnetic resonance (MR) images revealed an intradural pure cystic mass at the L3-L4 level. A radiologic diagnosis of spinal arachnoid cyst was established. Three years later, he complained of aggravated back pain, and follow-up MR examination showed a markedly expanded cyst, occupying the subarachnoid space from the T11 to the S1 level. L2 hemilaminectomy was performed, and a yellowish infected cyst bulged out through the dural opening. The cyst was removed en bloc. The histopathological findings of the cyst were consistent with parasitic infection. Serum enzyme-linked immunosorbent assay (ELISA) confirmed the presence of spinal cysticercosis. As there was no intracranial lesion, the final diagnosis was primary spinal cysticercosis, which is very rare. MR imaging is a sensitive diagnostic tool for detecting cystic lesions in the spine; however, it is difficult to distinguish cysticercosis from non-infectious cysts such as an arachnoid cyst without using gadolinium enhancement. Clinicians treating spinal cysts with an unusual clinical course should include cysticercosis as a differential diagnosis. We recommend contrast-enhanced MR imaging and serum ELISA in the diagnostic work-up of such cases.

摘要

我们描述了一例罕见的硬脊膜内髓外原发性脊髓囊尾蚴病。一名42岁男性因下背部疼痛前来我院就诊。他否认食用过生肉。磁共振(MR)图像显示L3 - L4水平有一个硬脊膜内单纯囊性肿块。初步诊断为脊髓蛛网膜囊肿。三年后,他主诉背痛加重,后续MR检查显示囊肿明显扩大,占据了从T11至S1水平的蛛网膜下腔。行L2半椎板切除术,一个淡黄色的感染性囊肿从硬脑膜开口处膨出。将囊肿完整切除。囊肿的组织病理学检查结果与寄生虫感染相符。血清酶联免疫吸附测定(ELISA)证实存在脊髓囊尾蚴病。由于没有颅内病变,最终诊断为原发性脊髓囊尾蚴病,这非常罕见。MR成像对于检测脊柱囊性病变是一种敏感的诊断工具;然而,在不使用钆增强的情况下,很难将囊尾蚴病与非感染性囊肿如蛛网膜囊肿区分开来。对于治疗具有不寻常临床病程的脊柱囊肿的临床医生,应将囊尾蚴病纳入鉴别诊断。我们建议在此类病例的诊断检查中进行对比增强MR成像和血清ELISA检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdf2/4094751/826c770030c6/jkns-55-226-g001.jpg

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