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图赖讷-索伦-戈勒综合征:需要识别其完整形式。

Touraine-Solente-Gole syndrome: The complete form needs to be recognized.

作者信息

Karnan Sudha, Krishnamoorthy Vanitha, Ethiraj Prabhu, Sathyanathan Babu Peter

机构信息

Barnard Institute of Radiology, Madras Medical College, Chennai, Tamil Nadu, India.

出版信息

Indian J Nucl Med. 2012 Jul;27(3):201-4. doi: 10.4103/0972-3919.112743.

Abstract

The primary hypertrophic osteoarthropathy (HOA) (pachydermoperiostosis) is a rare hereditary disease characterized by skin manifestations (pachydermia), digital clubbing and proliferation of periosteum (periostitis) with sub-periosteal new bone formation. We describe here a case who presented with seborrheic dermatitis and joint pain of both hands on work up matched satisfactorily with the complete form of primary HOA. The identification of secondary form being relatively common among clinicians and hence the importance of recognizing the primary form, which is a difficult to treat condition is discussed here.

摘要

原发性肥厚性骨关节病(HOA)(厚皮性骨膜病)是一种罕见的遗传性疾病,其特征为皮肤表现(厚皮症)、杵状指和骨膜增生(骨膜炎)伴骨膜下新骨形成。我们在此描述一例患者,该患者表现为脂溢性皮炎和双手关节疼痛,检查结果与原发性HOA的完全型相符。本文讨论了继发性形式在临床医生中相对常见,因此认识原发性形式的重要性,原发性形式是一种难以治疗的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8888/3728748/bbb79abca785/IJNM-27-201-g001.jpg

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