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Spontaneous and idiopathic chronic spinal epidural hematoma: two case reports and review of the literature

机译:自发性和特发性慢性脊髓硬膜外血肿:两个病例报告并文献复习

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摘要

Spinal epidural hematoma (SEH) represents the most frequent entity of acute or chronic spinal bleeding. Based upon pathogenesis, SEH can be classified as idiopathic, spontaneous, and secondary. The idiopathic forms are considered not to be attributed to any specific risk factors. Spontaneous SEH, accounting for 0.3–0.9% of all spinal epidural space occupying lesions, instead is associated with risk factors (such as substantial soft trauma or coagulation abnormalities). The chronic form, as our literature review revealed, is the rarest and its most frequent location is the lumbar spine. The pathophysiology of spontaneous and idiopathic SEH is still under debate: There are only a few reports in literature of chronically evolving SEH with progressively increasing pain and neurological impairment. Magnetic resonance imaging may be inconclusive for differential diagnosis. Here, we present two cases of lumbar chronic SEH with slow, progressive, and persistent lumbar radicular impairment. The first patient reported a minor trauma with slight back contusion and thus was classified as spontaneous SEH. In the second case not even a minor trauma was involved, so we considered it to be idiopathic SEH. In both cases preoperative blood and coagulation tests were normal and we did not find any other or co-factors in the patients’ clinical histories. MR imaging showed uncertain spinal canal obstructing lesions at L3 and L4 level in both cases. Surgical treatment allowed a correct diagnosis and resulted in full clinical and neuroradiological recovery after 1 year follow-up. Our aim is to discuss pathogenesis, clinical and radiological features, differential diagnosis and treatment options, on the background of relevant literature review.
机译:脊髓硬膜外血肿(SEH)代表急性或慢性脊髓出血的最常见实体。根据发病机理,SEH可分为特发性,自发性和继发性。特发性形式被认为不归因于任何特定的危险因素。自发性SEH占所有脊髓硬膜外腔占位病变的0.3-0.9%,而与危险因素(例如严重的软性创伤或凝血异常)相关。正如我们的文献综述所揭示的那样,慢性形式是最罕见的,其最常见的位置是腰椎。自发性和特发性SEH的病理生理学仍在争论中:文献中只有少数关于慢性发展的SEH伴随着疼痛和神经功能障碍逐渐加剧的报道。磁共振成像对于鉴别诊断可能不是决定性的。在这里,我们介绍了两例慢性,慢性,持续性,慢性和持续性腰根神经功能损害的SEH。第一位患者报告有轻微的外伤并伴有轻微的背部挫伤,因此被归为自发性SEH。在第二种情况下,甚至没有轻微的创伤,因此我们认为这是特发性SEH。在这两种情况下,术前血液和凝血检查均正常,我们在患者的临床病史中未发现任何其他因素或辅助因素。 MR成像均显示L3和L4水平的不确定的椎管阻塞性病变。手术治疗允许正确的诊断,并在一年的随访后导致临床和神经放射学的全面恢复。我们的目的是在相关文献综述的背景下讨论发病机理,临床和放射学特征,鉴别诊断和治疗选择。

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