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Successful Treatment of Idiopathic Thrombocytopenic Purpura After Liver Transplant: A Case Report
Idiopathic thrombocytopenic purpura, a common acquired bleeding disorder in pediatric patients, is an autoimmune disorder characterized by a low platelet count. Organ transplant can transfer such diseases, but the occurrence of idiopathic thrombocytopenic purpura after liver transplant is rare. Here...
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Published in: | Experimental and clinical transplantation 2020-10, Vol.18 (5), p.649-652 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Idiopathic thrombocytopenic purpura, a common
acquired bleeding disorder in pediatric patients, is an
autoimmune disorder characterized by a low platelet
count. Organ transplant can transfer such diseases,
but the occurrence of idiopathic thrombocytopenic
purpura after liver transplant is rare. Here, we report a
17-month-old girl who was diagnosed with idiopathic
thrombocytopenic purpura and who had a history
of liver transplant 11 months earlier. Treatment of
cytomegalovirus and Epstein-Barr virus infection led
to a successful outcome. |
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ISSN: | 1304-0855 2146-8427 |
DOI: | 10.6002/ect.2018.0083 |