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伴有瘤内出血的单纯性脊髓硬膜外海绵状血管瘤:胸椎脊髓病的罕见病因。

Pure spinal epidural cavernous hemangioma with intralesional hemorrhage: a rare cause of thoracic myelopathy.

作者信息

Jang Donghwan, Kim Choonghyo, Lee Seung Jin, Ryu Young-Joon, Kim Jiha

机构信息

Department of Neurosurgery, Kangwon National University Hospital, Chuncheon, Gangwon, Korea.

Department of Pathology, Kangwon National University Hospital, Chuncheon, Gangwon, Korea.

出版信息

Korean J Spine. 2014 Jun;11(2):85-8. doi: 10.14245/kjs.2014.11.2.85. Epub 2014 Jun 30.

DOI:10.14245/kjs.2014.11.2.85
PMID:25110490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4124926/
Abstract

Although cavernous hemangiomas occur frequently in the intracranial structures, they are rare in the spine. Most of spinal hemangiomas are vertebral origin and "pure" epidural hemangiomas not originating from the vertebral bone are very rare. Our spinal hemangioma case is extremely rare because of its "pure" epidural involvement and intralesional hemorrhage. A 64-year-old man presented with progressive paraparesis from two months ago. His motor weakness was rated as grade 4/5 in bilateral lower extremities. He also complained of decreased sensation below the T4 sensory dermatome, which continuously progressed to the higher dermatome level. Magnetic resonance imaging demonstrated thoracic spinal tumor at T3-T4 level. The tumor was located epidural space compressing thoracic spinal cord ventrally. The tumor was not involved with the thoracic vertebral bone. We performed T3-5 laminectomy and removed the tumor completely. The tumor was not infiltrating into intradural space or vertebral bone. The histopathologic study confirmed the epidural tumor as cavernous hemangioma. Postoperatively, his weakness improved gradually. Four months later, his paraparesis recovered completely. Here, we present a case of pure spinal epidural cavernous hemangioma, which has intralesional hemorrhage. We believe cavernous hemangioma should be included in the differential diagnosis of the spinal epidural tumors.

摘要

虽然海绵状血管瘤在颅内结构中经常出现,但在脊柱中却很罕见。大多数脊柱血管瘤起源于椎体,而“单纯”的非椎体起源的硬膜外血管瘤非常罕见。我们的脊柱血管瘤病例极为罕见,因为它是“单纯”的硬膜外受累且瘤内出血。一名64岁男性自两个月前开始出现进行性双下肢轻瘫。他双下肢的肌力减弱评定为4/5级。他还主诉T4感觉皮节以下感觉减退,并持续进展至更高的皮节水平。磁共振成像显示T3 - T4水平的胸椎肿瘤。肿瘤位于硬膜外间隙,腹侧压迫胸段脊髓。肿瘤未累及胸椎椎体。我们进行了T3 - 5椎板切除术并完全切除了肿瘤。肿瘤未浸润至硬膜内间隙或椎体。组织病理学研究证实硬膜外肿瘤为海绵状血管瘤。术后,他的无力症状逐渐改善。四个月后,他的双下肢轻瘫完全恢复。在此,我们报告一例伴有瘤内出血的单纯脊柱硬膜外海绵状血管瘤病例。我们认为海绵状血管瘤应纳入脊柱硬膜外肿瘤的鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6d/4124926/9239f81c70d4/kjs-11-85-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6d/4124926/20c856ddb2cc/kjs-11-85-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6d/4124926/9239f81c70d4/kjs-11-85-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6d/4124926/20c856ddb2cc/kjs-11-85-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c6d/4124926/9239f81c70d4/kjs-11-85-g002.jpg

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