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Spinal dumbbell-shaped epidural cavernous hemangioma (CM): report of nine surgical cases and literature review

机译:脊柱哑铃型硬膜外海绵状血管瘤(CM):9例手术报告并文献复习

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BackgroundSpinal dumbbell-shaped epidural cavernous malformation (CM) is a rare, hypervascular entity frequently misdiagnosed for other lesions, leading to unexpected intraoperative bleeding and suboptimal resection. Our study aims to elucidate the demographics, management strategy, and outcome of this vascular disease. MethodsRetrospective review of patients seen in Beijing Tiantan Hospital with symptomatic dumbbell-shaped epidural CM from 2008 to 2013. All lesions were pathologically confirmed after resection. The clinical manifestations, radiographic features, and treatment modalities of these cases were analyzed. ResultsWe included 9 consecutive patients. Average age was 58?±?12?years (range: 34–79?years), with 66.7% male. Locations of the CMs were: thoracic ( n =?7, 77.8%), cervical ( n =?1, 11.1%), and cervicothoracic junction ( n =?1, 11.1%). Only one case presented with acute manifestations while others experienced chronic progressive spinal cord symptoms. The initial clinical diagnoses were: schwannoma ( n =?6, 66.7%), cavernous hemangioma (CM) ( n =?1, 11.1%), meningioma ( n =?1, 11.1%), and angioma ( n =?1, 11.1%). Total resection was achieved in six patients (66.7%), and partial resection in the other three patients (33.3%). Average intraoperative blood loss was 400?±?300?ml (range: 100–1000?ml). During an average follow-up of 71?±?21?months (range: 29–94?months), excellent outcome was achieved in seven cases (77.8%), one partially improved (11.1%), and one deteriorated (11.1%). No patients experienced recurrence of symptoms. ConclusionsSpinal dumbbell-shaped epidural CM is a benign vascular malformation that should be differentiated from other dumbbell-shaped lesions. Accurate preoperative diagnose is challenging as no specific radiographic marker has been established. Total surgical resection should be recommended.
机译:背景脊柱哑铃形硬膜外海绵状畸形(CM)是一种罕见的血管过多实体,经常被误诊为其他病变,导致术中意外出血和切除效果欠佳。我们的研究旨在阐明这种血管疾病的人口统计学,治疗策略和结果。方法回顾性分析2008年至2013年在北京天坛医院有症状的哑铃型硬膜外CM患者的病情,所有病灶均在手术切除后经病理证实。分析了这些病例的临床表现,影像学特征和治疗方式。结果我们纳入了9名连续患者。平均年龄为58±12岁(范围:34-79岁),男性为66.7%。 CM的位置为:胸廓(n =?7,77.8%),颈椎(n =?1,11.1%)和颈胸腔交界处(n =?1,11.1%)。仅一例表现出急性表现,而其他则经历慢性进行性脊髓症状。最初的临床诊断为:神经鞘瘤(n =?6,66.7%),海绵状血管瘤(CM)(n =?1,11.1%),脑膜瘤(n =?1,11.1%)和血管瘤(n =?1)。 ,11.1%)。 6例(66.7%)实现了全切除,其他3例(33.3%)实现了部分切除。术中平均失血量为400?±?300?ml(范围:100–1000?ml)。在平均随访71±21个月(范围:29-94个月)期间,有7例(77.8%)获得了优异的结果,其中1例得到部分改善(11.1%),而1例恶化了(11.1%)。 )。没有患者出现症状复发。结论脊柱哑铃状硬膜外CM是一种良性血管畸形,应与其他哑铃状病变区别开来。由于尚未建立具体的放射学标记,因此准确的术前诊断具有挑战性。应建议进行全手术切除。

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