Volume 59, Issue 4 pp. 531-536
Original Articles: Gastroenterology

Anastomotic Ulcerations After Intestinal Resection in Infancy

Fabienne Charbit-Henrion

Corresponding Author

Fabienne Charbit-Henrion

Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital Necker-Enfants Malades, Vandoeuvre-les-Nancy, France

Address correspondence and reprint requests to Fabienne Charbit-Henrion, MD, Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital Necker-Enfants Malades, 149 rue de Sèvres, 75743 Paris, Cedex 15, France (e-mail: [email protected]).Search for more papers by this author
Christophe Chardot

Christophe Chardot

Department of Pediatric Surgery and Transplantation, Hôpital Necker-Enfants Malades, Vandoeuvre-les-Nancy, France

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Frank Ruemmele

Frank Ruemmele

Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital Necker-Enfants Malades, Vandoeuvre-les-Nancy, France

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Cécile Talbotec

Cécile Talbotec

Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital Necker-Enfants Malades, Vandoeuvre-les-Nancy, France

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Alain Morali

Alain Morali

Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital d'Enfants de Brabois, Vandoeuvre-les-Nancy, France

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Olivier Goulet

Olivier Goulet

Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital Necker-Enfants Malades, Vandoeuvre-les-Nancy, France

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Virginie Colomb

Virginie Colomb

Department of Pediatric Gastroenterology-Hepatology and Nutrition, Hôpital Necker-Enfants Malades, Vandoeuvre-les-Nancy, France

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First published: 01 October 2014
Citations: 34

The authors report no conflicts of interest.

ABSTRACT

Objective:

Anastomotic ulceration (AU) is a rare complication after intestinal resection and anastomosis, described mostly in children. The main symptom is occult bleeding, leading to iron-deficiency anemia, which is life threatening.

Methods:

The present survey reports a series of patients with AU after intestinal resection in infancy, focusing on predictive factors, medical and surgical treatment options, and long-term outcomes. Eleven patients (7 boys) born between 1983 and 2005 with AU after an intestinal resection and anastomosis in infancy were included in this retrospective review.

Results:

The diagnosis of AU was often delayed for several years. No predictive factor (including the primary disease, the length of the remnant bowel, and the loss of the ileocaecal valve) could be identified. Numerous treatment options, including antibiotics and anti-inflammatory drugs, proved to be ineffective to induce prolonged remission. Even after surgical resection, relapses were observed in 5/7 children.

Conclusions:

The mechanism leading to AU remains unknown. Contrary to previous reports with limited follow-up, no medical or surgical treatment could prevent recurrences. Because relapses may occur several years after treatment, long-term follow-up is needed.

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