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Published on: March 14, 2017
Severe Henoch-Schönlein purpura in a thalassemic patient under deferiprone treatment
Sule Unal1, Safak Gücer, Gülsev Kale
1Division of Pediatric Hematology, Faculty of Medicine, Hacettepe University, Ankara, Turkey. suleunal@hacettepe.edu.tr
Abstract:
Herein we present a 7-year-old beta-thalassemia major patient who developed severe Henoch-Schönlein purpura (HSP) with renal, pulmonary involvement and invagination while under iron chelation with deferiprone. DNA analysis for familial Mediterranean fever revealed M696V mutation. Various cellular and humoral immunological impairments have been described in thalassemia major patients and the severe course of HSP in our case may be related to these underlying immunological defects.
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