Literature DB >> 23343520

Cutaneous manifestations in patients with Wiskott-Aldrich syndrome submitted to haematopoietic stem cell transplantation.

Juliana Gomes Loyola Presa1, Vania Oliveira de Carvalho, Laura Rogers Morrisey, Carmem Maria Bonfim, Kerstin Taniguchi Abagge, Angélica Vasselai, Leide Parolin Marinoni.   

Abstract

INTRODUCTION: Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency caused by a mutation of the WAS protein gene. This protein actively participates in important cellular processes, and its presence is related to diverse clinical manifestations, including cutaneous alterations. The classical triad of WAS consists of recurrent infections, thrombocytopaenia with small platelets and atopic dermatitis (AD)-like lesions.
OBJECTIVE: To evaluate the frequencies of cutaneous manifestations in patients with WAS prior to haematopoietic stem cell transplantation (HSCT).
RESULTS: Twenty-four boys diagnosed with WAS and treated with HSCT between 1992 and 2007 were included. The characteristic triad of WAS occurred in 46% of patients. Before HSCT, the most frequent cutaneous manifestations included eczema similar to AD (71%), followed by petechiae and/or ecchymosis (58%) and cutaneous infections (17%).
CONCLUSIONS: Cutaneous manifestations in patients with WAS are frequent, especially those similar to the eczema found in AD.

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Year:  2013        PMID: 23343520     DOI: 10.1136/archdischild-2011-300812

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  1 in total

Review 1.  Common dermatologic manifestations of primary immune deficiencies.

Authors:  Manisha Relan; Heather K Lehman
Journal:  Curr Allergy Asthma Rep       Date:  2014-12       Impact factor: 4.919

  1 in total

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