Epidural angiolipoma and Andersson lesion: A rare co-occurence—A case report and literature review

Q4 Medicine
S. Vijayan, Christopher Gerber, Anindya Basu, Garga Basu, Radhika Mhatre
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引用次数: 0

Abstract

Spinal angiolipomas (SALs) are very rare benign extradural neoplasms, representing 0.14%–1.2% of all spinal tumors. Andersson lesion is a localized vertebral or disco-vertebral lesion in ankylosing spondylitis. Co-occurrence of these lesions is very rare and has never been reported. We are reporting one such case of a 61-year-old man presented with features of dorsal compressive myelopathy. On magnetic resonance imaging (MRI), he was diagnosed to have a SAL at D6–D9 and Andersson lesion at D7–D8 and L1–L2. He was managed surgically with a long-segment fixation and decompression and gross total excision of the tumor. Diagnosis of a SAL was confirmed in a biopsy, and postoperatively, he showed good clinical improvement. In conclusion, given the rarity of co-occurrence of these pathologies, a strong clinical suspicion is required. MRI and CT scan help in diagnosis. Both these pathologies warrant surgical management. When diagnosed early and managed appropriately, they have a good prognosis.
硬膜外血管脂肪瘤合并Andersson病变:罕见的合并症1例报告并文献复习
脊髓血管脂肪瘤(SALs)是一种非常罕见的良性硬膜外肿瘤,约占脊髓肿瘤的0.14%-1.2%。Andersson病变是强直性脊柱炎的局部椎体或椎间盘病变。这些病变的同时发生是非常罕见的,从未报道过。我们报告一例61岁男性表现为脊背压迫性脊髓病。在磁共振成像(MRI)上,他被诊断为D6-D9有SAL, D7-D8和L1-L2有Andersson病变。他接受手术治疗,采用长节段固定减压和肿瘤全切除。活检证实了SAL的诊断,术后,他表现出良好的临床改善。总之,鉴于罕见的这些病理同时发生,强烈的临床怀疑是必要的。MRI和CT扫描有助于诊断。这两种病理都需要手术治疗。如果早期诊断和适当处理,他们有良好的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Indian Spine Journal
Indian Spine Journal Medicine-Surgery
CiteScore
0.40
自引率
0.00%
发文量
18
审稿时长
25 weeks
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