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What’s the resolutive surgery for pseudo-ainhum in Vohwinkel syndrome? A case report and review of the literature

Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant autosomal keratosis. It typically presents with “starfish” keratoses on the knuckles, palmoplantar keratoderma (PPK), hearing impairment and mutilating digital constriction bands (pseudoainhum) that ca...

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Detalles Bibliográficos
Autores principales: Rovere, Giuseppe, Stramazzo, Leonardo, Cioffi, Alessio, Galvano, Nicolò, Pavan, Davide, Restuccia, Giuseppe, D’Arienzo, Antonio, Capanna, Rodolfo, Maccauro, Giulio, D’Arienzo, Michele, Camarda, Lawrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883105/
https://www.ncbi.nlm.nih.gov/pubmed/33633820
http://dx.doi.org/10.4081/or.2020.8868
Descripción
Sumario:Vohwinkel Syndrome, also known as Keratoderma Hereditarium Mutilans, is an extremely rare dominant autosomal keratosis. It typically presents with “starfish” keratoses on the knuckles, palmoplantar keratoderma (PPK), hearing impairment and mutilating digital constriction bands (pseudoainhum) that cause strangulation, often leading to autoamputation of the affected digit. Both medical and surgical treatment haven’t shown to date consistent results, in the treatment of pseudoainhum. In this study we present the case of a woman with Vohwinkel syndrome who showed constriction bands causing ischemic changes of the 5th digit of the right hand for which she was treated with surgery. We also present a review of the literature for the management of this disease.