皮埃尔-玛丽-班贝格综合征:一个独特的病例报告

S. Abbas
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引用次数: 0

摘要

收稿日期:2019年3月25日修稿日期:2019年5月14日接受发表2019年6月6日通讯:Syed Ahsan Abbas FMH医学和牙科学院卡苏尔。摘要肥厚性骨关节病(HOA)由friedrich于1868年提出。这是一种罕见的疾病,表现多样,包括脚趾和手指的棒状,伴有水肿的关节痛,双侧上睑下垂,皮肤增厚和狮子相。骨和关节周围组织增生导致四肢扩张。它是多种肿瘤(副肿瘤综合征)中的一种远端病变;O常与肺肿瘤有关。我们报告一例36岁的巴基斯坦男性吸烟者,在一般检查中表现为双侧关节疼痛,呼吸急促和4级数字棒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pierre Marie-Bamberger Syndrome: A unique case report
Received: 25 March 2019 Revised: 14 May 2019 Accepted for publication 6 June 2019 Correspondence: Syed Ahsan Abbas FMH College of Medicine and Dentistry Kasur. E-mail:ahsanzileali@gmail.com Abstract Hypertrophic osteoarthropathy (HOA) was described by Friedreich in 1868. It is a rare condition with variable presentations including clubbing of the toes and ngers, arthralgia with edema, bilateral ptosis, thickening of the skin and leonine facies. Bone and periarticular tissue proliferation leads to expansive extremities. It is a distant e ect disorder in various neoplasms (paraneoplastic syndrome); o en associated with lung neoplasm. We report a case of a 36 year old Pakistani male smoker, presenting with bilateral joint pains, shortness of breath and grade 4 digital clubbing on general examination.
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