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一名成年患者的椎体朗格汉斯细胞组织细胞增多症:病例报告及文献复习

Vertebral Langerhans cell histiocytosis in an adult patient: case report and review of the literature.

作者信息

Sapkas George, Papadakis Michael

机构信息

University of Athens and the Metropolitan Hospital, Athens, Greece.

出版信息

Acta Orthop Belg. 2011 Apr;77(2):260-4.

Abstract

Vertebral Langerhans cell histiocytosis, formerly called Histiocytosis X, is rarely seen in adults: a systematic non-quantitative review of the literature yielded only 27 cases. Vertebra plana is often associated in children, but this is not a feature in the adult population. The authors report the case of a 29-year-old woman with a two-month history of lumbar pain. Osteolysis of the right pedicle of L2 was noted on CT and MRI. Transpedicular curettage and fusion L1L3 were performed. Histopathological examination revealed Langerhans cell histiocytosis. Although rare, Langerhans cell histiocytosis should be included in the differential diagnosis of the solitary lytic vertebral lesion in the adult. Good results have been reported, in the absence of systemic manifestations, with the most conservative approach possible.

摘要

脊椎朗格汉斯细胞组织细胞增多症,以前称为组织细胞增多症X,在成人中很少见:对文献进行的系统非定量综述仅发现27例。扁平椎在儿童中常与之相关,但在成人中并非如此。作者报告了一名29岁女性的病例,该患者有两个月的腰痛病史。CT和MRI检查发现L2右侧椎弓根骨质溶解。进行了经椎弓根刮除术和L1-L3融合术。组织病理学检查显示为朗格汉斯细胞组织细胞增多症。尽管罕见,但朗格汉斯细胞组织细胞增多症应纳入成人孤立性溶骨性椎体病变的鉴别诊断。在没有全身表现的情况下,采用尽可能保守的方法已报告有良好效果。

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