| Literature DB >> 33177052 |
Eirini Kyrana1, David Rees2, Florence Lacaille3, Emer Fitzpatrick4, Mark Davenport5, Nigel Heaton6, Sue Height7, Marianne Samyn8, Fulvio Mavilio9, Valentine Brousse10, Abid Suddle11, Subarna Chakravorty7,12, Anita Verma11, Girish Gupte13, Marki Velangi14, Baba Inusa15, Emma Drasar16, Nedim Hadzic8, Tassos Grammatikopoulos4,17, Jonathan Hind4, Maesha Deheragoda17, Maria Sellars18, Anil Dhawan19.
Abstract
Liver involvement in sickle cell disease (SCD) is often referred to as sickle cell hepatopathy (SCH) and is a complication of SCD which may be associated with significant mortality. This review is based on a round-table workshop between paediatric and adult hepatologists and haematologists and review of the literature. The discussion was prompted by the lack of substantial data and guidance in managing these sometimes very challenging cases. This review provides a structured approach for the diagnosis and management of SCH in children and young adults. The term SCH describes any hepatobiliary dysfunction in the context of SCD. Diagnosis and management of biliary complications, acute hepatic crisis, acute hepatic sequestration and other manifestations of SCH are discussed, as well as the role of liver transplantation and haemopoietic stem cell transplantation in the management of SCH. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: adolescent health; gastroenterology; jaundice
Mesh:
Year: 2020 PMID: 33177052 PMCID: PMC7610372 DOI: 10.1136/archdischild-2020-319778
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791