Iliescu B F, Chiriţă B C, Poeată I
Prof. Dr. N. Oblu Clinical Emergency Hospital, FAculty of Medicine.
Rev Med Chir Soc Med Nat Iasi. 2013 Oct-Dec;117(4):947-53.
Lumbar spinal epidural lesions could belong to a wide spectrum of pathologies. However, some cases present with rare conditions that can cause significant neurological deficit and raise serious diagnostic challenges. We present two such cases where the clinical picture and the imaging findings failed to elucidate the actual diagnosis, which came as an intraoperative and pathological surprise.
The first case is that of a 78-years-old male that presented for low back pain, bilateral S1 radicular sciatica, paraparesis, and difficulty walking. The neurologic exam showed the absence of the rotulian reflexes bilaterally, and a partial sensory loss in the crural dermatomes. The MRI showed an epidural mass, contrast enhancing at the L1-L2 level, suggestive for an extraxial tumor. The second case is that of a 62-year-old woman that presented for a hyperalgic sciatica involving the right S1 root with parestesias in the corresponding dermatome. MRI showed a cystic, contrast enhancing lesion in the L5-S1 recess, mimicking a cystic neuroma. Both patients underwent surgery and histopathological exams were performed from the excised pieces.
In the first case the surgery resulted in complete removal of the pathological process and histopathological result returned chronic organized hematoma, concordant with the intraoperatory aspect. The evolution was good. In the second case the histopathological result came back as pulpous disk. Again the evolution was good with complete neurological recovery.
In the presence of an epidural mass with clear clinical symptomatology, rare entities like chronic epidural hematoma or posterior migrated disk material should be always considered as a differential diagnosis in patients with suspicion of extradural chronic compressions. In these cases, only the intraoperatory and histopathological exams can provide a clear diagnosis.
腰椎硬膜外病变可能属于多种不同的病理情况。然而,有些病例呈现出罕见病症,可导致严重的神经功能缺损并带来严峻的诊断挑战。我们报告两例此类病例,其临床表现和影像学检查结果均未能明确实际诊断,而最终诊断是术中及病理检查时意外发现的。
第一例是一名78岁男性,表现为腰痛、双侧S1神经根性坐骨神经痛、下肢轻瘫及行走困难。神经系统检查显示双侧髌阵挛消失,小腿皮节有部分感觉丧失。MRI显示L1-L2水平有一硬膜外肿块,增强扫描有强化,提示为轴外肿瘤。第二例是一名62岁女性,表现为牵涉右侧S1神经根的疼痛性坐骨神经痛,相应皮节有感觉异常。MRI显示L5-S1隐窝有一囊性、增强扫描有强化的病变,类似囊性神经瘤。两名患者均接受了手术,并对切除组织进行了组织病理学检查。
第一例手术成功完全切除病变组织,组织病理学结果为慢性机化血肿,与术中所见相符。病情进展良好。第二例组织病理学结果为髓核突出。同样,病情进展良好,神经功能完全恢复。
对于有明确临床症状的硬膜外肿块患者,在怀疑硬膜外慢性压迫时,应始终将慢性硬膜外血肿或后移椎间盘组织等罕见情况作为鉴别诊断考虑。在这些病例中,只有术中及组织病理学检查才能提供明确诊断。