Literature DB >> 20465619

Vohwinkel syndrome: treatment of pseudo-ainhum.

Franco Bassetto1, Cesare Tiengo, Rossella Sferrazza, Anna Belloni-Fortina, Mauro Alaibac.   

Abstract

BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis which manifests in infants and becomes more evident in adulthood. Patients with this mutation present hyperkeratosis of the palms and soles, constricting bands of the digits, usually at the fifth, and starfish-shaped hyperkeratosis on the dorsal aspects of the hands and feet. The disease mostly occurs in white women, where constricting fibrous bands appear on the digits and can lead to progressive strangulation and auto-amputation (pseudo-ainhum). AIM: The treatment of this keratoderma is very difficult and tends to be symptomatic: topical keratolytics and systemic retinoids have been used to treat hyperkeratosis, but without consistent results. Reconstructive surgery is utilized for the treatment of pseudo-ainhum. RESULTS AND
CONCLUSION: In this study, we present an additional case of Vohwinkel syndrome in which constrictive bands of the fifth digit in the left hand were treated with a cross finger flap, with a favorable outcome after 18 months of follow-up.

Entities:  

Mesh:

Year:  2010        PMID: 20465619     DOI: 10.1111/j.1365-4632.2009.04267.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  12 in total

1.  Hanging on by a thread: a rare case of secondary pseudoainhum.

Authors:  Leo Arkush; Bernadette De Silva; David Gordon
Journal:  BMJ Case Rep       Date:  2016-02-02

2.  Vohwinkel syndrome: ichthyosiform variant in a family.

Authors:  Clarissa Prieto Herman Reinehr; Juliano Peruzzo; Tania Cestari
Journal:  An Bras Dermatol       Date:  2018 Sep-Oct       Impact factor: 1.896

3.  Successful surgical management of keratoderma hereditaria mutilans.

Authors:  Jared J Liebman; Yuan Liu
Journal:  Hand (N Y)       Date:  2013-03

4.  Ainhum - A Rare Case Report.

Authors:  Ravi Prabhu; Narayanasamy Subbaraju Kannan; Sundaresan Vinoth; Chinnappan Balasubramanian Praveen
Journal:  J Clin Diagn Res       Date:  2016-04-01

5.  [Vohwinkel syndrome. Hearing loss and keratoderma on the hands and feet].

Authors:  S Dippold; F Butsch; R Schopf; A Keilmann
Journal:  HNO       Date:  2013-07       Impact factor: 1.284

6.  Vohwinkel syndrome, ichthyosiform variant--by Camisa--case report.

Authors:  Liliam Dalla Corte; Mariana Vale Scribel da Silva; Carina Flores de Oliveira; Gerson Vetoratto; Raquel Bissacotti Steglich; Josiane Borges
Journal:  An Bras Dermatol       Date:  2013 Nov-Dec       Impact factor: 1.896

7.  Unique autosomal recessive variant of palmoplantar keratoderma associated with hearing loss not caused by known mutations.

Authors:  Moustafa Abdelaal Hegazi; Sommen Manou; Hazem Sakr; Guy Van Camp
Journal:  An Bras Dermatol       Date:  2017       Impact factor: 1.896

8.  Ainhum, a rare mutilating dermatological disease in a female Cameroonian: a case report.

Authors:  Diego Nitcheu Tchouakam; Joel Noutakdie Tochie; Marc Leroy Guifo; Simeon Pierre Choukem
Journal:  BMC Dermatol       Date:  2019-08-12

9.  Vohwinkel's Syndrome: A Rare Disorder of Keratinization.

Authors:  Nidhi Choudhary; Rahul Ahar; Abhishek De; Projna Biswas
Journal:  Indian J Dermatol       Date:  2014-11       Impact factor: 1.494

10.  Using a Distant Abdominal Skin Flap to Treat Digital Constriction Bands: A Case Report for Vohwinkel Syndrome.

Authors:  Mingzi Zhang; Kexin Song; Ning Ding; Chang Shu; Youbin Wang
Journal:  Medicine (Baltimore)       Date:  2016-02       Impact factor: 1.817

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