| Literature DB >> 25135271 |
Vitorino Modesto dos Santos1, Thiago Pereira Loures2, João Daniel Bringel Rego3, Christiane Aires Teixeira4, Kayursula Dantas de Carvalho5, Afonso Lucas Oliveira Nascimento6.
Abstract
Pachyonychia congenital (PC) is a rare autosomal dominant genodermatosis characterized hyperkeratosis affecting the nails and palmoplantar areas, oral leukokeratosis, and cystic lesions. A 39-year-old woman with PC type 1 (Jadassohn-Lewandowsky syndrome) and B-cell lymphoma is described. No similar disorders or parental consanguinity were found in her family. Typical features of PC developed since her early childhood and the diagnosis of B-cell lymphoma was established seven years ago, without a clear causal relation between these entities. Despite inherent limitations of a single case, this report may contribute to PC understanding.Entities:
Mesh:
Year: 2014 PMID: 25135271
Source DB: PubMed Journal: Acta Med Iran ISSN: 0044-6025