Dilip Chand Raja S, Kanna Rishi Mugesh, Shetty Ajoy Prasad, Rajasekaran S
Department of Spine Surgery, 313 Mettupalayam Road, Ganga Hospital, Coimbatore, India.
Case Rep Orthop. 2018 Oct 22;2018:1945149. doi: 10.1155/2018/1945149. eCollection 2018.
Osteolipomas are uncommon variants of lipoma. These lesions have been usually reported to arise from the oral cavity, brain, and neck and scarcely from the knee and thigh. Intraspinal osteolipomas are rare. A single case of intraspinal osteolipoma has been reported in the cervical and thoracic spine in the literature. To our knowledge, there is no report of osteolipomas in the lumbar spine.
We report a very rare case of a solitary lumbar intraspinal osteolipoma, presenting as a cauda equina syndrome. The intraspinal osteolipoma was excised en bloc and fusion was performed as it required partial resection of the facet joint within 24 hours of presentation. He has since then improved neurologically, and there has been no recurrence of the lesion so far. The clinical presentation, radiological characteristics, treatment course, and histopathological features of this lesion along with the clinical outcomes and a pertinent literature review were done and have been discussed.
The heterogeneous signal intensity of the lesion in MRI differentiates it from other dural-based lesions, and this should raise suspicion of an osteolipoma, which warrants a CT. Although intraspinal osteolipomas are benign lesions and generally have good prognosis, they need to be removed en bloc as they may result in rapid neurological deterioration.
骨脂肪瘤是脂肪瘤的罕见变异类型。这些病变通常据报道起源于口腔、脑和颈部,很少起源于膝关节和大腿。椎管内骨脂肪瘤很罕见。文献中曾报道过1例颈椎和胸椎的椎管内骨脂肪瘤。据我们所知,尚无腰椎骨脂肪瘤的报道。
我们报告1例非常罕见的孤立性腰椎椎管内骨脂肪瘤病例,表现为马尾综合征。该椎管内骨脂肪瘤在发病24小时内整块切除,并因需要部分切除小关节而进行了融合手术。此后他的神经功能有所改善,且迄今为止病变未复发。我们对该病变的临床表现、影像学特征、治疗过程、组织病理学特征以及临床结果进行了分析,并结合相关文献进行了讨论。
MRI上病变的异质性信号强度使其与其他硬膜源性病变相鉴别,这应引起对骨脂肪瘤的怀疑,需进行CT检查。尽管椎管内骨脂肪瘤是良性病变且通常预后良好,但因其可能导致神经功能迅速恶化,故需整块切除。