Title of article :
Pericardial Graft vs. Host Disease in a Patient with β-Thalassemia Major
Author/Authors :
Saravi, Mehrdad Department of Cardiology - Babol University of Medical Sciences , Vakili Sadeghi, Mohsen Department of Hematology - Babol University of Medical Sciences , Mahmoodi Nesheli, Hassan Non-Communicable Pediatrics Diseases Research Center - Babol University of Medical Sciences
Pages :
3
From page :
674
To page :
676
Abstract :
Bone marrow transplantation (BMT) in young children improves results in β-thalassemia major. Graft versus host disease (GVHD) is an important complication of peripheral blood stem cell transplantation. GVHD affects heart with a behavior resembling an autoimmune disease, including pericardial effusion. We describe a 22-year-old β-thalassemia major patient who underwent bone marrow transplantation with an HLA-identical sibling donor. The patient didn’t have any serious problem until 15 months after transplantation. He presented with chest discomfort and progressive dyspnea. Early echocardiogram showed mild pericardial effusion. Four days later, the effusion had increased, impending to cardiac temponade requiring pericardectomy. Immunospressive drugs and pericardectomy resulted in significant improvement in ventricular filling. Cardiac cGVHD, an un-common complication of HSCT may be presented as pericardial effusion. Although early initiation of steroids is very important, heart monitoring is necessary to diagnose cardiac temponade. Keywords:
Keywords :
BMT , β thalassemia major , GVHD , HSCT , pericarditis
Journal title :
Archives of Iranian Medicine
Serial Year :
2016
Record number :
2515793
Link To Document :
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