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Ozyoruk D.,Ankara Childrens Hematology and Oncology Education and Research Hospital | Kibar A.E.,Ankara Childrens Hematology and Oncology Education and Research Hospital | Surucu M.,Ankara Childrens Hematology and Oncology Education and Research Hospital | Azak E.,Ankara Childrens Hematology and Oncology Education and Research Hospital | And 2 more authors.
Pediatric Transplantation | Year: 2015

PH is a rare condition with high mortality rate after pediatric HSCT. As clinical presentation is non-specific and may mimic other conditions, a high degree of suspicion is required for diagnosis. Here, we present a patient with stage-IV neuroblastoma who developed PAH after autologous HSCT. After exclusion of other causes of PH, we regarded that this condition was secondary to HSCT. © 2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd

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