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腰椎硬膜外海绵状血管瘤:一例报告并文献复习

Lumbar Epidural Cavernous Hemangioma: A Case Report and Review of the Literature.

作者信息

Kienzler Jenny C, Hidalgo Teresa E, Wichmann Werner, Magagna-Poveda Alejandra, Fandino Javier

机构信息

Neurosurgery, Kantonsspital Aarau, Aarau, CHE.

Pediatric Neurosurgery, New York University Langone Health, New York, USA.

出版信息

Cureus. 2023 Jan 12;15(1):e33677. doi: 10.7759/cureus.33677. eCollection 2023 Jan.

Abstract

Pure epidural cavernous hemangioma (ECH) of the spine are rare and account for only 4% of all epidural spinal lesions. We report a case of epidural cavernoma at L3/4 presenting with L4 radiculopathy. Radiological, intraoperative findings and histopathology are presented. We present the case of a 56-year-old man who was admitted with a right L4 radiculopathy including an M4 paresis of the right leg, hypoesthesia L4, and radicular pain. Magnetic resonance imaging (MRI) confirmed an extradural lesion L3/4 partially expanding into the right intervertebral foramen. The lesion had a heterogeneous signal, isointense on T1-weighted and hyperintense on proton density (PD) and T2-weighted images. At surgery, an epidural, ovoid, gray-red, soft mass, lightly adherent to the dura and extending to the right L4 foramen was observed. Findings in the histological examination indicated a cavernous hemangioma without signs of hemorrhage. Symptoms and paresis improved rapidly after surgery. The follow-up MRI showed complete resection of the lesion with no signs of radicular compression. Spinal ECH should be considered as a cause of chronic lumbar radiculopathy with atypical radiological findings. Early diagnosis and total removal of the spinal ECH might prevent hemorrhage and neurological deficits. Fewer than 50 cases of lumbar epidural spinal hemangioma have been reported until today, and our case report is adding valuable knowledge to the existing literature.

摘要

脊柱单纯性硬膜外海绵状血管瘤(ECH)罕见,仅占所有硬膜外脊柱病变的4%。我们报告一例L3/4节段硬膜外海绵状血管瘤伴L4神经根病的病例。文中展示了影像学、术中发现及组织病理学情况。我们报告的病例为一名56岁男性,因右侧L4神经根病入院,表现为右腿M4级轻瘫、L4感觉减退及神经根性疼痛。磁共振成像(MRI)证实L3/4节段硬膜外病变,部分扩展至右侧椎间孔。该病变信号不均,在T1加权像上呈等信号,在质子密度(PD)加权像和T2加权像上呈高信号。手术中,可见一个硬膜外、椭圆形、灰红色、质地柔软的肿块,与硬脊膜轻度粘连,延伸至右侧L4椎间孔。组织学检查结果显示为海绵状血管瘤,无出血迹象。术后症状和轻瘫迅速改善。随访MRI显示病变完全切除,无神经根受压迹象。脊柱ECH应被视为具有非典型影像学表现的慢性腰椎神经根病的病因之一。早期诊断并完全切除脊柱ECH可能预防出血和神经功能缺损。迄今为止,报道的腰椎硬膜外脊柱血管瘤病例少于50例,我们的病例报告为现有文献增添了有价值的知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f8/9918856/67fbd1b6bdfa/cureus-0015-00000033677-i01.jpg

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