完全性柏氏畸形:病例报告

IF 1 Q3 MEDICINE, GENERAL & INTERNAL Electronic Journal of General Medicine Pub Date : 2024-01-01 DOI:10.29333/ejgm/13900
Mohd Firdaus Abdul Mubing, Razlina Abdul Rahman, Salziyan Badrin, Hasni Ibrahim
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引用次数: 0

摘要

糙皮病(PDP)又称 Touraine-Solente-Gole 综合征或原发性肥大性骨关节病,是一种非常罕见的疾病,主要特征为糙皮病、手指弯曲、多汗症和骨膜增生。我们报告了一例患者的病例,尽管他接受了多家诊所的治疗,但 25 年来,他的双手和双脚逐渐出现疼痛和肿大。他的面部和头皮也逐渐出现异常变化。下肢的放射影像显示骨膜下骨质增生和骨膜肥厚。由于完全性 PDP 的罕见性和医疗从业人员对这一诊断的不熟悉,该病例很晚才被确诊。该病例突出表明,医务人员需要了解罕见疾病,以便尽早对患者进行诊断和治疗,从而减轻他们的焦虑,提高他们的生活质量。
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Complete pachydermoperiostosis: A case report
Pachydermoperiostosis (PDP), also known as Touraine-Solente-Gole syndrome or primary hypertrophic osteoarthropathy, is a very rare disease mainly characterized by pachyderma, finger clubbing, hyperhidrosis, and periostosis. We reported a case of a patient who suffered from gradual pain and enlargement of both hands and feet for 25 years despite receiving treatment from multiple clinics. He also experienced gradual abnormal changes in his face and scalp. Radiographic images of the lower limbs revealed the presence of subperiosteal bone growth and periosteal hypertrophy. The diagnosis of complete PDP was made late due to its rarity and the unfamiliarity of medical practitioners with the diagnosis. This case highlighted the need for medical practitioners to be aware of rare diseases so that patients may be diagnosed and treated earlier and thereby relieving their anxiety and improve their quality of life.
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来源期刊
Electronic Journal of General Medicine
Electronic Journal of General Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
3.60
自引率
4.80%
发文量
79
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