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小儿脊柱多灶性朗格汉斯细胞组织细胞增多症:一例报告及文献复习

Multifocal Langerhans cell histiocytosis of the pediatric spine: a case report and literature review.

作者信息

Vadivelu S, Mangano F T, Miller C R, Leonard J R

机构信息

Department of Neurosurgery, St. Louis Children's Hospital, Washington University in St. Louis, One Children Place,St. Louis, MO 63110, USA.

出版信息

Childs Nerv Syst. 2007 Jan;23(1):127-31. doi: 10.1007/s00381-006-0172-x. Epub 2006 Sep 20.

Abstract

CASE REPORT

An 11-month-old boy presented with a 3-month history of lower extremity weakness. CT and MRI of the spine revealed an enhancing epidural mass, extending from T1 through T5 and exiting through multiple foramina. The largest extraspinal extent was located at the T3 vertebral level and was accompanied by complete T3 vertebral collapse. A second lytic lesion at the L2 vertebral body without an obvious enhancing mass was also noted. Open biopsy and decompression of the spinal cord were performed, and histopathological analysis revealed a mixed inflammatory lesion with abundant S-100 and CD1a immunoreactive Langerhans cells consistent with the diagnosis of Langerhans cell histiocytosis (LCH).

DISCUSSION

The authors present a very rare pediatric case of spinal LCH causing spinal cord compression. Possible clues to early detection, consideration of differential diagnoses, and a brief literature review are presented.

摘要

病例报告

一名11个月大的男童出现下肢无力3个月。脊柱CT和MRI显示硬膜外肿块强化,从T1延伸至T5,并通过多个椎间孔穿出。最大的椎管外范围位于T3椎体水平,并伴有T3椎体完全塌陷。还发现L2椎体有第二个溶骨性病变,无明显强化肿块。进行了开放性活检和脊髓减压,组织病理学分析显示为混合性炎症病变,有丰富的S-100和CD1a免疫反应性朗格汉斯细胞,符合朗格汉斯细胞组织细胞增多症(LCH)的诊断。

讨论

作者报告了一例非常罕见的小儿脊柱LCH导致脊髓受压的病例。文中给出了早期检测的可能线索、鉴别诊断的考虑因素,并进行了简要的文献综述。

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