Kabi F, Mkinsi O, Janani S, Raissouni N
Service de Rhumatologie, CHU Ibn-Rochd, Casablanca, Maroc.
Rev Med Interne. 2006 Sep;27(9):710-2. doi: 10.1016/j.revmed.2006.04.019. Epub 2006 Jun 5.
The pachydermoperiostosis (PDP) or primitive hypertrophic osteoarthropathy (HOA) is a rare hereditary disease.
We report a 22-year-old man born to consanguineous marriage who presented presented with PDP. This patient disclosed an arthropathy, a clubbing, a diffuse periostosis, and a pachyderma of the hands, the feet and the forehead. All the examinations that were performed to look for an etiology remained negative. Diagnosis of PDP was considered and the patient treated with colchicine.
We discuss the diagnostic issues raised by PDP, especially with the secondary HOA and chronic inflammatory rheumatisms.
厚皮性骨膜病（PDP）或原发性肥厚性骨关节病（HOA）是一种罕见的遗传性疾病。
我们报告一名22岁男性，其父母为近亲结婚，患有PDP。该患者表现出关节病、杵状指、弥漫性骨膜增生以及手部、足部和前额部的厚皮症。为寻找病因所进行的所有检查结果均为阴性。考虑诊断为PDP，并对该患者使用秋水仙碱进行治疗。
我们讨论了PDP引发的诊断问题，尤其是与继发性HOA和慢性炎症性风湿病相关的问题。
