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Camptodactyly: From Embryological Basis to Surgical Treatment

Camptodactyly is a relatively rare hand deformity presenting as the proximal interphalangeal joint’s nontraumatic and progressive flexion contracture. Most cases are limited to the fifth finger. The severity and type of camptodactyly should be considered to optimize treatment. Since many structures...

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Detalles Bibliográficos
Autores principales: Kloc, Jan, Dzula, Boris, Varga, Ivan, Klein, Martin, Steno, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221293/
https://www.ncbi.nlm.nih.gov/pubmed/37241199
http://dx.doi.org/10.3390/medicina59050966
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author Kloc, Jan
Dzula, Boris
Varga, Ivan
Klein, Martin
Steno, Boris
author_facet Kloc, Jan
Dzula, Boris
Varga, Ivan
Klein, Martin
Steno, Boris
author_sort Kloc, Jan
collection PubMed
description Camptodactyly is a relatively rare hand deformity presenting as the proximal interphalangeal joint’s nontraumatic and progressive flexion contracture. Most cases are limited to the fifth finger. The severity and type of camptodactyly should be considered to optimize treatment. Since many structures at the finger base can be involved in the pathogenesis of the deformity, surgical treatment for this particular type of deformity is challenging. This paper aims to bring insight into camptodactyly’s pathogenesis and treatment options. We discuss the indication and pitfalls of surgical treatment options for particular camptodactyly types and present a case of a fourteen-year-old boy who was admitted to our department with proximal interphalangeal joint flexion contracture of the left fifth digit.
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spelling pubmed-102212932023-05-28 Camptodactyly: From Embryological Basis to Surgical Treatment Kloc, Jan Dzula, Boris Varga, Ivan Klein, Martin Steno, Boris Medicina (Kaunas) Case Report Camptodactyly is a relatively rare hand deformity presenting as the proximal interphalangeal joint’s nontraumatic and progressive flexion contracture. Most cases are limited to the fifth finger. The severity and type of camptodactyly should be considered to optimize treatment. Since many structures at the finger base can be involved in the pathogenesis of the deformity, surgical treatment for this particular type of deformity is challenging. This paper aims to bring insight into camptodactyly’s pathogenesis and treatment options. We discuss the indication and pitfalls of surgical treatment options for particular camptodactyly types and present a case of a fourteen-year-old boy who was admitted to our department with proximal interphalangeal joint flexion contracture of the left fifth digit. MDPI 2023-05-17 /pmc/articles/PMC10221293/ /pubmed/37241199 http://dx.doi.org/10.3390/medicina59050966 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Kloc, Jan
Dzula, Boris
Varga, Ivan
Klein, Martin
Steno, Boris
Camptodactyly: From Embryological Basis to Surgical Treatment
title Camptodactyly: From Embryological Basis to Surgical Treatment
title_full Camptodactyly: From Embryological Basis to Surgical Treatment
title_fullStr Camptodactyly: From Embryological Basis to Surgical Treatment
title_full_unstemmed Camptodactyly: From Embryological Basis to Surgical Treatment
title_short Camptodactyly: From Embryological Basis to Surgical Treatment
title_sort camptodactyly: from embryological basis to surgical treatment
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221293/
https://www.ncbi.nlm.nih.gov/pubmed/37241199
http://dx.doi.org/10.3390/medicina59050966
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