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Intranodal capillary-cavernous hemangioma: Report of a very rare case

机译:颅内毛细血管海绵状血管瘤:极少数病例报告

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摘要

Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation of capillaries and cavernous vessels filled with erythrocytes and lined by endothelial cells. Magnetic resonance imaging with enhanced and T2 STIR sequences is the most efficient imaging for diagnosing this type of hemangioma. Rarely, malignancy or another vascular lesion can be evoked as a differential diagnosis of mixed hemangioma. Treatment in this localization is often surgical, even if other possibilities exist for other areas. In this article, we describe a very rare case of intranodal capillary-cavernous hemangioma.
机译:混合型毛细血管海绵状血管瘤是一种罕见的血管异常,其节内定位极为罕见。其发现通常是偶然的,但可能是临床症状。诊断依赖于组织病理学,显示毛细血管和海绵状血管的增生,充满了红细胞并被内皮细胞衬里。具有增强的T1和T2 STIR序列的磁共振成像是诊断这种类型血管瘤的最有效成像。很少有恶性肿瘤或其他血管病变可作为混合型血管瘤的鉴别诊断。即使在其他区域存在其他可能性,这种局限性治疗也通常是外科手术。在本文中,我们描述了极少见的结节内毛细血管海绵状血管瘤病例。

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