PDF(Pubmed)
Abstract：
UNASSIGNED: Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy showed a good initial response in our patient.
UNASSIGNED: Pachydermoperiostosis (PDP) is a rare genetic disorder with unclear etiopathogenesis. We report a case of a 38-year-old male who presented with classic features of PDP. Our patient showed a good initial response to etoricoxib therapy but the safety and efficacy over long-term use are yet to be determined in further studies.
UNASSIGNED: Pachydermoperiostosis (PDP) is a rare genetic disorder with unclear etiopathogenesis. We report a case of a 38-year-old male who presented with classic features of PDP. Our patient showed a good initial response to etoricoxib therapy but the safety and efficacy over long-term use are yet to be determined in further studies.
摘要：
■厚皮骨肥大症是一种罕见的遗传性疾病，与肢端肥大症非常相似。诊断通常基于不同的临床和放射学特征。口服依托考昔治疗在我们的患者中显示出良好的初始反应。
■厚皮骨膜病（PDP）是一种罕见的遗传性疾病，病因不明。我们报告了一例38岁男性，具有PDP的经典特征。我们的患者对依托考昔治疗有良好的初始反应，但长期使用的安全性和有效性尚待进一步研究确定。
■厚皮骨膜病（PDP）是一种罕见的遗传性疾病，病因不明。我们报告了一例38岁男性，具有PDP的经典特征。我们的患者对依托考昔治疗有良好的初始反应，但长期使用的安全性和有效性尚待进一步研究确定。
