A Rare Instance of Spinal Cord Cavernous Malformation With Adjacent Intramedullary Microhemorrhage.

Le Yu, Cuiping Mu, Huanting Li, Yugong Feng, Zhenwen Cui
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Abstract

The natural history of spinal cord cavernous malformation (SCM) may be characterized by recurrent episodes of hemorrhage resulting in a range of neurologic deficits, most of which are microhemorrhage and subsequent gliosis that can lead to progressive myelopathy. Macrohemorrhage with acute onset of symptoms is extremely rare and leads to irreversible neurologic deficits. In this article, we present an unusual case of ruptured cavernous malformation (CM) in the cervical spinal cord with large extralesional hemorrhage. The patient underwent an operation of posterior longitudinal myelotomy and had a good neurologic recovery. A histologic examination revealed the typical features of cavernous angioma.
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脊髓空洞畸形并伴有髓内微出血的罕见病例
脊髓空洞畸形(SCM)的自然病史特点可能是反复发作的出血导致一系列神经功能缺损,其中大多数是微出血和随后的胶质细胞病变,可导致进行性脊髓病变。急性发作的大出血极为罕见,会导致不可逆的神经功能缺损。本文介绍了一例不寻常的颈脊髓海绵畸形(CM)破裂伴大腔外出血的病例。患者接受了后纵髓切断术,神经功能恢复良好。组织学检查显示了海绵状血管瘤的典型特征。
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