Volume 59, Issue 5 pp. 562-564
Original Articles: Gastroenterology

Clinical Patterns and Outcome of Early-Onset Inflammatory Bowel Disease

Oren Ledder

Oren Ledder

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia

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Anthony G. Catto-Smith

Anthony G. Catto-Smith

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia

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Mark R. Oliver

Mark R. Oliver

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia

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George Alex

George Alex

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia

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Donald J.S. Cameron

Donald J.S. Cameron

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia

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Winita Hardikar

Corresponding Author

Winita Hardikar

Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Parkville, Victoria, Australia

Address correspondence and reprint requests to Winita Hardikar, FRACP, PhD, Department of Gastroenterology, Royal Children's Hospital, 50 Flemington Rd, Parkville, Vic 3052, Australia (e-mail [email protected]).Search for more papers by this author
First published: 01 November 2014
Citations: 24

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The authors report no conflicts of interest.

ABSTRACT

We sought to determine whether extremely-early-onset childhood inflammatory bowel disease (age <6 years; 20 ulcerative colitis [UC], 8 Crohn disease [CD], 2 indeterminate, sequentially diagnosed) was clinically more severe than in older children (6–17 years; 19 UC, 39 CD, 2 indeterminate). Early-onset UC was marked by less abdominal pain at presentation, but an aggressive course with a significant reduction in weight-for-age, increased use of immunosuppressants, and more surgery. Children with early-onset CD were more likely to have bloody stools at presentation and an isolated colitis. This study supports the suggestion that inflammatory bowel disease phenotype differs in early-onset disease.

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