指浅屈肌腱起源异常致强直1例并文献复习

IF 0.8 Q4 SURGERY Surgery Journal Pub Date : 2019-10-01 DOI:10.1055/s-0039-1697631
S. Duci
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引用次数: 1

摘要

摘要Camptodactyly是一种近端指间关节屈曲挛缩症,是一种孤立的畸形,在人群中影响1/300,可以作为一种常染色体显性遗传,具有可变表达。一名17岁女性因右手小指弯曲首次被转诊至普里什蒂纳科索沃大学临床中心整形外科诊所。她表现为右小指近端指间关节进行性屈曲挛缩大于110度。根据我们在门诊会诊中的观察结果,我们得出结论,小手指弯曲灵活(>110度)的病例接受了手术治疗,取得了良好的效果。因此,我们认为在我们的病例报告中使用的手术技术将有助于治疗这种复杂的畸形。
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Camptodactyly Caused by an Anomalous Origin of the Flexor Digitorum Superficialis Tendon: A Case Report and Review of the Literature
Abstract Camptodactyly is a flexion contracture of the proximal interphalangeal joints and is known as an isolated malformation that affects 1 in 300 in the population and can be inherited as an autosomal dominant trait with variable expression. A 17-year-old female was referred to the Clinic of Plastic Surgery, University Clinical Center of Kosovo, Prishtina, for the first time with camptodactyly of the little finger in the right hand. She was presented with a progressive flexion contracture of the proximal interphalangeal joint greater than 110 degrees of her right little finger. According to our observations from outpatient consultations, we concluded that the case of camptodactyly in the little finger in the flexible form (>110 degrees), which underwent surgical treatment, presented excellent result. Therefore, we think that the surgical technique used in our case report will contribute to treating this complicated deformity.
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来源期刊
Surgery Journal
Surgery Journal SURGERY-
自引率
0.00%
发文量
64
审稿时长
12 weeks
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