X-Linked Agammaglobulinemia Presenting with Secondary Hemophagocytic Syndrome: A Case Report

Bibliographic Details
Title: X-Linked Agammaglobulinemia Presenting with Secondary Hemophagocytic Syndrome: A Case Report
Authors: Can Ozturk, Sumer Sutcuoglu, Berna Atabay, Afig Berdeli
Source: Case Reports in Medicine, Vol 2013 (2013)
Publisher Information: Hindawi Limited, 2013.
Publication Year: 2013
Collection: LCC:Medicine
Subject Terms: Medicine
More Details: Introduction. Coincidence of X-linked agammaglobulinemia (XLA) and secondary hemophagocytic syndrome (sHS) is atypical. Both diseases are rare and pathogenesis of the latter one is not clearly known. Case Presentation. A 5-year-old boy was diagnosed both with XLA and sHS. However, in his history, he did not have severe and recurrent infections. Bruton tyrosine kinase (BTK) gene mutation was present (c.1581_1584delTTTG). To the best of the authors’ knowledge, coincidence of XLA and sHS had not been reported in the literature before. Conclusion. Patients with XLA are extremely vulnerable to recurrent bacterial infections. The diagnosis of XLA with sHS at any time of life is both an interesting and challenging situation without history of recurrent bacterial infections.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1687-9627
1687-9635
Relation: https://doaj.org/toc/1687-9627; https://doaj.org/toc/1687-9635
DOI: 10.1155/2013/742795
Access URL: https://doaj.org/article/a027426bacdd4c8b9b0c6a65d28ab978
Accession Number: edsdoj.027426bacdd4c8b9b0c6a65d28ab978
Database: Directory of Open Access Journals
More Details
ISSN:16879627
16879635
DOI:10.1155/2013/742795
Published in:Case Reports in Medicine
Language:English