A Case of Mal De Meleda: The Rare Presentation of Palmoplantar Keratoderma Disease.

clinical dermatology mal de meleda palmoplantar keratoderma rare diseases scleroatrophic erythema

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Sep 2021
Historique:
accepted: 17 09 2021
entrez: 25 10 2021
pubmed: 26 10 2021
medline: 26 10 2021
Statut: epublish

Résumé

Mal de Meleda (MDM) is a rare sub-type of palmoplantar keratoderma (PPK) disease. The primary symptoms of PPK are scleroatrophy, transient keratoderma, scleroatrophic erythema, pseudoainhum around the digits, and perioral erythema. MDM is a pathology with a difficult clinical course. This case study presents two cases of MDM in siblings born out of second-degree consanguinity. The presenting complaint was the peeling of the palmar skin since birth. Both patients were treated with acitretin orally (dose: 10 mg) for three months and tretinoin (topical) for two months. The prognosis was good after three months of treatment.

Identifiants

pubmed: 34692287
doi: 10.7759/cureus.18061
pmc: PMC8523366
doi:

Types de publication

Case Reports

Langues

eng

Pagination

e18061

Informations de copyright

Copyright © 2021, Kalyan et al.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Vamsi Kalyan (V)

Medicine and Surgery, Rangaraya Medical College, Kakinada, IND.

Tarun K Suvvari (TK)

Medicine and Surgery, Dr. N.T.R University of Health Sciences, Vijayawada, IND.

Venkata Dinesh Kumar Kandula (VDK)

Medicine, GSL Medical College, Rajahmundry, IND.

Aparajeya Shanker (A)

Faculty of Medicine, Medical University of Pleven, Pleven, BGR.

Lolita Matiashova (L)

Department of Comprehensive Risk Reduction for Chronic Non-Communicable Diseases, L.T. Malaya Therapy National Institute of the National Academy of Medical Sciences of Ukraine, Kharkiv, UKR.

Classifications MeSH