Case Reports

Is Reye’s syndrome still a valid diagnosis?

Lorraine du Toit-Prinsloo, Philip Snyman, Gert Saayman

Abstract


Reye’s syndrome is characterised by acute non-inflammatory encephalopathy and fatty degeneration of the liver. The exact aetiology of the syndrome is unknown, but there is an association with viral infections and the use of aspirin. There has been a sharp decline in the incidence of Reye’s syndrome; the reasons for this are unclear, but may be due, in part, to the declining use of aspirin in children and to improvements in the diagnosis of underlying inborn errors of metabolism. The use of the term ‘Reye-like’ has been advocated among experts in the field. 

We report the case of a child with Reye-like syndrome complicated by pancreatitis.


Authors' affiliations

Lorraine du Toit-Prinsloo, Department of Forensic Medicine, University of Pretoria, South Africa

Philip Snyman, Department of Paediatrics, Kalafong Hospital, University of Pretoria, South Africa

Gert Saayman, Department of Forensic Medicine, University of Pretoria, South Africa

Full Text

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Keywords

Reye's syndrome; Reye-like; pancreatitis; fatty changes in the liver

Cite this article

South African Journal of Child Health 2014;8(2):75-77. DOI:10.7196/SAJCH.664

Article History

Date submitted: 2013-09-15
Date published: 2014-04-25

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