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Camptodactyly: An unsolved area of plastic surgery

  • Singh, Veena (Department of Burns & Plastic Surgery, All India Institute of Medical Sciences Patna) ;
  • Haq, Ansarul (Department of Burns & Plastic Surgery, All India Institute of Medical Sciences Patna) ;
  • Priyadarshini, Puja (Department of Burns & Plastic Surgery, All India Institute of Medical Sciences Patna) ;
  • Kumar, Purshottam (Department of General Surgery, All India Institute of Medical Sciences Patna)
  • 투고 : 2017.04.14
  • 심사 : 2018.06.22
  • 발행 : 2018.07.15

초록

Background Camptodactyly refers to permanent flexion contracture at the proximal interphalangeal joint. Most cases are limited to fifth-finger involvement. Although common, the treatment of camptodactyly is controversial. Many published studies have emphasized conservative treatment, while others have described surgical procedures. The problem with this deformity is that it presents in several forms, which means that there is no single model for effective treatment. The aim of this paper is to present the difficulties encountered with this condition and the management thereof on an individual basis. Methods This is a case series of 14 patients (nine males, five females) who underwent surgical treatment. The results were classified using the method from Mayo Clinic as excellent, good, fair, and poor. Results Fourteen patients with 15 fingers underwent surgery, and the results achieved were as follows: excellent, 0; good, 1; fair, 6; poor, 8. The treatment of camptodactyly still remains controversial, and hence proper planning individualized to each patient is needed to achieve the maximal improvement with realistic goals. Conclusions Although we performed individualised surgery, our careful follow-up was not able to identify any method as superior over another with respect to gain in extension and loss of flexion. We therefore propose that the extensor mechanism should not be disturbed during surgery to treat camptodactyly cases.

키워드

참고문헌

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피인용 문헌

  1. Dupuytren's contracture: Concise approach to an enigmatic disease vol.5, pp.3, 2019, https://doi.org/10.4103/ijam.ijam_12_19