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朗格汉斯细胞组织细胞增多症所致单灶性股骨肉芽肿:一例报告并文献复习

Unifocal Granuloma of Femur due to Langerhans' Cell Histiocytosis: A Case Report and Review of the Literature.

作者信息

Singh Harpreet, Kaur Satnam, Yuvarajan P, Jain Nishant, Maini Lalit

机构信息

Department of Orthopaedics, Maulana Azad Medical College and associated Lok Nayak Hospital, Delhi 110002, India.

出版信息

Case Rep Med. 2010;2010. doi: 10.1155/2010/686031. Epub 2010 Aug 9.

Abstract

The radiological diagnosis of osteolytic lesions of the long bones in pediatric population constitutes a challenge when the case history and clinical data are uncharacteristic. We believe that the description of few clinically and histologically proven cases to verify the existence of radiological signs useful for diagnosis may be of interest. Here, we describe a case of Langerhans' cell histiocytosis (LCH) presenting as unifocal eosinophilic granuloma of femur along with a brief review of the literature.

摘要

当病史和临床数据不典型时,儿科人群长骨溶骨性病变的放射学诊断构成一项挑战。我们认为,描述一些经临床和组织学证实的病例,以验证有助于诊断的放射学征象的存在,可能会有意义。在此,我们描述一例表现为股骨单灶性嗜酸性肉芽肿的朗格汉斯细胞组织细胞增多症(LCH)病例,并对文献进行简要回顾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b4/2929637/bf6a30634d8a/CRM2010-686031.001.jpg

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