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Rare presentation of juvenile xanthogranuloma in the thoracic spine of an adult patient: case report and literature review

机译:成年患者胸椎中少见的黄色肉芽肿瘤的病例报告和文献复习

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摘要

Isolated spinal involvement of juvenile xanthogranuloma (JXG) is extremely rare. There are only seven prior published cases of spinal JXG, of which only one has been reported in an adult. We report here the eighth case of spinal JXG and the second in an adult. The patient, a 22-year-old female, presented with progressive upper backache. Radiological examination revealed a well-defined osteolytic hypointense mass in the T7 vertebral body, with a large soft tissue paraspinal extension causing cord compression. Complete resection of the mass was performed, with resolution of symptoms. Histology showed a histiocytic tumour with numerous Touton, foreign body and osteoclastic giant cells, immunopositive for CD68 and vimentin and negative for S100 and CD1a, corresponding to a diagnosis of JXG. Literature regarding spinal JXG is reviewed and discussed.
机译:少年性黄原肉芽肿(JXG)的单独脊柱受累极为罕见。以前只有7例脊柱JXG病例,成人中只有1例。我们在此报告第八例脊柱JXG病例,第二例成人。该患者为22岁女性,表现为进行性上背痛。放射学检查发现T7椎体中有明确的溶骨性低眼质,并伴有较大的软组织椎旁延伸,导致脊髓受压。完全切除肿块,症状缓解。组织学显示组织细胞性肿瘤具有大量Touton,异物和破骨细胞巨细胞,对CD68和波形蛋白免疫阳性,对S100和CD1a免疫阴性,对应于JXG的诊断。脊柱JXG的文献进行了审查和讨论。

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