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Pulmonary arterial hypertension in a child with stage‐ IV neuroblastoma after autologous hematopoietic stem cell transplantation and review of the literature
Author(s) -
Özyörük Derya,
Kibar Ayşe Esin,
Sürücü Murat,
Azak Emine,
Emir Suna,
Çetin İbrahim İlker,
Tunç Bahattin,
Özbek Namık Yaşar
Publication year - 2015
Publication title -
pediatric transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 69
eISSN - 1399-3046
pISSN - 1397-3142
DOI - 10.1111/petr.12576
Subject(s) - medicine , neuroblastoma , hematopoietic stem cell transplantation , stage (stratigraphy) , presentation (obstetrics) , pulmonary hypertension , stem cell , transplantation , hematopoietic stem cell , surgery , haematopoiesis , paleontology , genetics , biology , cell culture
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 .

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