Mal de Meleda‐like Palmoplantar Keratoderma
- 1 January 1991
- journal article
- case report
- Published by Wiley in The Journal of Dermatology
- Vol. 18 (1) , 43-46
- https://doi.org/10.1111/j.1346-8138.1991.tb03038.x
Abstract
A 38-year-old Japanese man was seen for severe palmoplantar keratoderma, extending to the dorsal aspects with red rims. He had had spontaneous amputations of the toes and surgical amputation of the right lower leg because of squamous cell carcinoma of the right sole. The clinical symptoms suggested those of mal de Meleda, except for the absence of consanguinity and of granular layers in the epidermis. The keratoderma improved with oral etretinate treatment.Keywords
This publication has 3 references indexed in Scilit:
- Olmsted syndrome—congenital palmoplantar and periorificial keratodermaJournal of the American Academy of Dermatology, 1984
- Genetic tylosis with malignancy: a study of a South Indian pedigreeBritish Journal of Dermatology, 1980
- MAL DE MELEDAArchives of Dermatology and Syphilology, 1939