Department of Orthopaedic Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan.
Department of Pathology, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan.
BMC Musculoskelet Disord. 2022 May 30;23(1):508. doi: 10.1186/s12891-022-05463-x.
Chronic spinal epidural hematomas (SEHs) are rare clinical entities. SEH with vertebral scalloping is extremely rare, with only a few cases having been reported to date. We report a unique case of spontaneous chronic SEH in the lumbar spine with severe vertebral scalloping mimicking an epidural tumor.
A 71-year-old man presented with a 2-month history of lumbar pain and a 3-week history of paresthesia and pain in the right lower extremity, hypesthesia in the perineal and perianal regions, and bladder dysfunction. Computed tomography following myelography revealed an epidural mass lesion on the right side that compressed the dural sac and was associated with severe bony scalloping on the posterior wall of the L4 vertebral body. Magnetic resonance imaging (MRI) on T1- and T2-weighted images revealed a space-occupying lesion with heterogeneous intensity, and T1-gadolinium images showed an intralesional heterogeneous enhancement effect. A tumoral lesion in the spinal canal was suspected, based on preoperative imaging; therefore, a total spinal tumor resection was planned. Intraoperative findings revealed that the brownish lesion adhered to the dura and epidural tissues in the spinal canal, and the space-occupying mass in the scalloped cavity of the posterior wall of the L4 vertebra was encapsulated in red-brownish soft tissues. The lesion was totally resected in a piecemeal fashion, and pathological examination revealed a mixture of tissues that contained a relatively new hematoma with hemoglobin, as well as an obsolete hematoma with hemosiderin and amyloid deposits. The mass was diagnosed as a chronic epidural hematoma with recurrent hemorrhage. The postoperative course was uneventful, and the preoperative neurological symptoms immediately improved.
The preoperative diagnosis of chronic SEHs is challenging, as MRI results may not be conclusive, particularly in patients with scalloping of bony structures. Thus, chronic SEHs should be considered as a differential diagnosis in cases of suspected tumoral lesions in the spinal canal. To the best of our knowledge, this is the first reported case of acute exacerbation of chronic SEH with cauda equina syndrome and severe vertebral scalloping.
慢性脊柱硬膜外血肿(SEH)是一种罕见的临床病症。伴有椎体切迹的 SEH 极为罕见,迄今为止仅报道了少数病例。我们报告了一例独特的自发性慢性腰椎 SEH 病例,其表现为严重的硬膜外肿瘤样椎体切迹。
一名 71 岁男性,因腰痛 2 个月,右下肢麻木和疼痛 3 周,会阴部和肛周感觉减退,膀胱功能障碍而就诊。脊髓造影后的计算机断层扫描显示右侧硬膜外肿块压迫硬脊膜,并伴有 L4 椎体后壁严重骨切迹。T1 和 T2 加权磁共振成像(MRI)显示占位性病变呈不均匀强度,T1 钆造影图像显示腔内不均匀强化效应。根据术前影像学检查,怀疑为椎管内肿瘤病变,因此计划进行全脊柱肿瘤切除术。术中发现,棕色病变与椎管内硬脊膜和硬膜外组织粘连,L4 椎体后壁切迹腔的占位性肿块被包裹在棕红色软组织中。病变被整块切除,病理检查显示组织混合物,其中含有相对较新的含血红蛋白血肿,以及陈旧性含铁血黄素和淀粉样沉积的血肿。该肿块被诊断为慢性硬膜外血肿伴复发性出血。术后过程顺利,术前神经症状立即改善。
慢性 SEH 的术前诊断具有挑战性,因为 MRI 结果可能不具结论性,尤其是在存在骨结构切迹的患者中。因此,对于疑似椎管内肿瘤病变的病例,应将慢性 SEH 作为鉴别诊断。据我们所知,这是首例伴有马尾综合征和严重椎体切迹的慢性 SEH 急性加重的报道。