دورية أكاديمية
أعرض في EDS

Mirror Foot: Surgical Approach for Esthetic and Functional Improvement.

التفاصيل البيبلوغرافية
العنوان: Mirror Foot: Surgical Approach for Esthetic and Functional Improvement.
المؤلفون: Guerra LA; Departamento de Ortopedia e Traumatologia, Hospital das Clínicas da Universidade Federal de Goiás/Empresa Brasileira de Serviços Hospitalares (EBSERH), Goiânia, GO, Brasil., Martins JS; Unidade do Sistema Músculoesquelético, Hospital das Clínicas da Universidade Federal de Goiás/Empresa Brasileira de Serviços Hospitalares (EBSERH), Goiânia, GO, Brasil.; Grupo de Pé e Tornozelo do Hospital das Clínicas da Universidade Federal de Goiás/Empresa Brasileira de Serviços Hospitalares (EBSERH), Goiânia, GO, Brasil., Lehnen IMP; Departamento de Ortopedia e Traumatologia, Hospital das Clínicas da Universidade Federal de Goiás/Empresa Brasileira de Serviços Hospitalares (EBSERH), Goiânia, GO, Brasil., Rodrigues GF; Departamento de Ortopedia e Traumatologia, Hospital das Clínicas da Universidade Federal de Goiás/Empresa Brasileira de Serviços Hospitalares (EBSERH), Goiânia, GO, Brasil., Santana LFB; Departamento de Ortopedia e Traumatologia, Hospital das Clínicas da Universidade Federal de Goiás/Empresa Brasileira de Serviços Hospitalares (EBSERH), Goiânia, GO, Brasil.
المصدر: Revista brasileira de ortopedia [Rev Bras Ortop (Sao Paulo)] 2022 Feb 15; Vol. 59 (3), pp. e462-e466. Date of Electronic Publication: 2022 Feb 15 (Print Publication: 2024).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Thieme Country of Publication: Germany NLM ID: 0123326 Publication Model: eCollection Cited Medium: Print ISSN: 0102-3616 (Print) Linking ISSN: 01023616 NLM ISO Abbreviation: Rev Bras Ortop (Sao Paulo) Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: 2019- : [Stuttgart] : Thieme
Original Publication: São Paulo : Sociedade Brasileira de Ortopedia e Traumatologia
مستخلص: Mirror foot is a rare congenital anomaly on to the spectrum of complex foot polydactyly. It may occur in isolation or associated with other malformations or genetic syndromes. This is a subject little described in the literature, with few publications on its treatment. We herein report the case of a 4-year-old female patient who presented with a left foot with 8 fingers, without other associated deformities, whose complaints included the impossibility of wearing shoes and social stigma. Radiographically, eight metatarsi with their respective phalanges, five cuneiform bones, and absence of bone deformities in the hindfoot were verified. The surgical approach was chosen in order to promote functional and esthetic improvement, as well as a better adaptation to the use of closed shoes, according to the patient's and family's desire. A dorsal and plantar V incision was performed, with resection of three supranumerary rays, including three central metatarsi with their nine corresponding phalanges, two cuneiform bones, tendons and extra digital nerves, followed by suture of the intermetatarsal ligaments, preserving the fingers with normal appearance, decreasing the width of the foot, and maintaining proper support. The reduction was maintained through transmetatarsal fixation with Kirschner wires. The postoperative period went on with the use of a walking boot and zero load, without complications, with removal o the Kirschner wires and allowing load on the limb after twelve weeks.
Competing Interests: Conflito de Interesses Os autores declaram não haver conflito de interesses.
(The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit ( https://creativecommons.org/licenses/by/4.0/ ).)
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فهرسة مساهمة: Keywords: bone wires; congenital foot deformities; polydactyly
تواريخ الأحداث: Date Created: 20240624 Latest Revision: 20240625
رمز التحديث: 20240625
مُعرف محوري في PubMed: PMC11193576
DOI: 10.1055/s-0042-1742341
PMID: 38911886
قاعدة البيانات: MEDLINE
الوصف
تدمد:0102-3616
DOI:10.1055/s-0042-1742341