Literature DB >> 27617521

Successful treatment of pityriasis lichenoides chronica with narrow-band ultraviolet B therapy in a patient with Keratitis-Ichthyosis-Deafness syndrome: a case report.

Andac Salman1, Dilek Seckin Gencosmanoglu, Ayse Deniz Yucelten, Nursel Elcioglu, Gabriele Richard, Cuyan Demirkesen.   

Abstract

Keratitis-ichthyosis-deafness (KID) syndrome is a rare genodermatosis causing ichthyosis-like skin lesions, keratitis, and deafness. Herein, we report a patient with this rare syndrome in association with pityriasis lichenoides chronica, which was succesfully treated with narrow-band ultraviolet B phototherapy despite our concerns regarding the increased risk of squamous cell carcinoma, hyperpyrexia, and keratitis.

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Year:  2016        PMID: 27617521

Source DB:  PubMed          Journal:  Dermatol Online J        ISSN: 1087-2108


  2 in total

1.  The Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of GJB2 Gene in 3 Members of a Family Is Similar to That of Clouston Syndrome.

Authors:  Yanjiang Xu; Minhua Wang; Ling Huang; Jie Hu
Journal:  Ann Dermatol       Date:  2022-10       Impact factor: 0.722

2.  KID Syndrome and Hidradenitis Suppurativa: A Rare Association Responding to Surgical Treatment.

Authors:  Vincenzo Bettoli; Riccardo Forconi; Ilaria Pezzini; Ruby Martinello; Valeria Scuderi; Piera Zedde; Natale Schettini; Lucrezia Pacetti; Monica Corazza
Journal:  Skin Appendage Disord       Date:  2020-10-26
  2 in total

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