| Literature DB >> 24281860 |
Francesco De Leonardis1, Roberta Koronica, Stefania D Bruno, Nicola Santoro.
Abstract
Hepatic sinusoidal obstructive syndrome (HSOS) is a frequent complication in patients undergoing haematopoietic stem cell transplant (HSCT), and more rarely, in paediatric patients receiving conventional chemotherapy for solid tumours. Its diagnosis relies on a combination of clinical signs and symptoms such as hepatomegaly, jaundice, weight gain and fluid retention. HSOS treatment is primarily based on supportive care and anti-fibrinolytic agents. Here we report two patients affected by Wilms tumour who developed life-threatening HSOS that failed to respond to conventional treatment. Both patients recovered after receiving aggressive supportive treatment that included administration of non-activated protein C (Ceprotin®--Baxter).Entities:
Keywords: Wilms tumour; chemotherapy; support care; veno-occlusive disease
Mesh:
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Year: 2013 PMID: 24281860 DOI: 10.1002/pbc.24859
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167