Dupuytren病

Jeremiah D. Johnson, Colin Pavano, Craig M. Rodner
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引用次数: 0

摘要

Dupuytren病是一种影响手部掌筋膜的纤维增殖性疾病,可导致手指屈曲挛缩。它最初是在北欧人群中被描述出来的,它的名字来源于法国外科医生Baron Dupuytren博士,他是最早就这种疾病发表演讲的人之一。Dupuytren病的病因尚不清楚,但可能受遗传和环境因素的影响。老年人和男性患此病的风险最大。Dupuytren病是一种临床诊断,患者通常表现为逐渐恶化的屈曲挛缩。通常观察到轻微的疾病,但对于衰弱性挛缩首选手术治疗。各种手术技术已被描述,包括切开或切除病变筋膜。总的来说,手术在矫正挛缩和改善功能方面是有效的,但尽管治疗成功,一些患者仍然会复发。最近,胶原酶注射和经皮手术已被用于治疗Dupuytren病,并在选定的患者中取得了令人鼓舞的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dupuytren’s Disease
Dupuytren’s disease is a fibroproliferative disease affecting the palmar fascia of the hand and leading to flexion contractures of the digits. It was first described in Northern European populations and derived its namesake from Dr. Baron Dupuytren, a French sur - geon, who was one of the first to lecture on the disease. The etiology of Dupuytren’s dis ease is unclear but is likely influenced by both genetic and environmental factors. Older individuals and men are most at risk of developing the disease. Dupuytren’s disease is a clinical diagnosis and patients often present with gradually worsening flexion contrac - tures. Mild disease is usually observed, but surgical treatment is preferred for debilitat ing contractures. A variety of surgical techniques have been described involving either incising or excising diseased fascia. Overall, surgery is effective in correcting contractures and improving function, but despite successful treatment some patients still experience recurrence. More recently, collagenase injections and percutaneous procedures have been utilized to treat Dupuytren’s disease and have yielded promising results in select patients.
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