Literature DB >> 25135271

A case with pachyonychia congenita and B-cell lymphoma.

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.

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Year:  2014        PMID: 25135271

Source DB:  PubMed          Journal:  Acta Med Iran        ISSN: 0044-6025


  1 in total

1.  Pachyonychia Congenita Type 1: Case Report and Review of the Literature.

Authors:  Praveen Kumar Rathore; Varun Khullar; Anupam Das
Journal:  Indian J Dermatol       Date:  2016 Mar-Apr       Impact factor: 1.494

  1 in total

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