Thoracic Intra and Extramedullary Capillary Hemangioma with Subacute Clinical Course: A Case Report and Literature Review

Yumeki Yamamoto, Hiroya Shimauchi-Ohtaki, Fumiaki Honda, Takahiro Shirakura, Keigo Aramaki, Ryosuke Shintoku, T. Miyagishima, Masanori Aihara, Hideaki Yokoo, Y. Yoshimoto
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Abstract

Capillary hemangiomas are benign tumors comprising a lobulated proliferation of capillary vessels frequently located in the soft tissues of the neck and head. Spinal intradural capillary hemangiomas are rare, particularly intramedullary lesions. To our knowledge, only 31 cases of spinal intramedullary capillary hemangiomas have been reported. Here, we describe a rare case of a thoracic capillary hemangioma comprising extramedullary and intramedullary components. A 51-year-old male patient presented with bilateral lower extremity numbness and subsequent paraparesis, sensory disturbance, and bladder-bowel dysfunction with a subacute clinical course. Magnetic resonance imaging revealed a mass lesion with intramedullary and intradural extramedullary components at the Th9-10 vertebrae level and widespread spinal cord edema. Contrast-enhanced computed tomography revealed abnormal vessels on the dorsal spinal cord surface. Spinal angiography revealed a light-stained mass lesion fed by the radiculopial artery from the right Th11 intercostal artery. The tumor was resected en bloc, and the histological diagnosis was a capillary hemangioma. Postoperatively, the spinal cord edema diminished, and the patient was discharged from the convalescent rehabilitation ward. Although intramedullary capillary hemangioma is a rare spinal tumor and its preoperative diagnosis is difficult, it should be considered in the differential diagnosis of spinal intramedullary tumors.
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胸腔髓内和髓外毛细血管瘤,临床过程呈亚急性:病例报告和文献综述
毛细血管瘤是一种良性肿瘤,由经常位于颈部和头部软组织的毛细血管分叶状增生组成。脊髓硬膜内毛细血管瘤非常罕见,尤其是髓内病变。据我们所知,目前仅有31例脊髓髓内毛细血管瘤的报道。在此,我们描述了一例罕见的胸腔毛细血管瘤病例,该病例包含髓外和髓内成分。一名 51 岁的男性患者出现双下肢麻木,随后出现截瘫、感觉障碍和膀胱-肠道功能障碍,临床过程呈亚急性。磁共振成像显示,Th9-10椎体水平存在髓内和髓外肿块病变,脊髓广泛水肿。对比增强计算机断层扫描显示脊髓背侧表面血管异常。脊髓血管造影显示,右侧Th11肋间动脉的桡动脉供应了一个光染肿块病灶。肿瘤被整体切除,组织学诊断为毛细血管瘤。术后,脊髓水肿减轻,患者从康复疗养病房出院。虽然髓内毛细血管瘤是一种罕见的脊柱肿瘤,术前诊断也很困难,但在脊柱髓内肿瘤的鉴别诊断中应将其考虑在内。
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