Background and aims: Anastomotic ulceration (AU) is a rare potential life-threatening complication that may occur after intestinal resection. The diagnosis is often delayed after a long-lasting history of refractory anemia. The pathogenesis remains unknown and there are no established therapies. The aim of the study was to analyze the medical history of children with short bowel syndrome (SBS) who were experiencing AU.Methods: Records of SBS children were retrospectively reviewed. Demographics, baseline characteristics, presentation, diagnosis and treatment of AU cases were analyzed.Results: Eight out of 114 children with SBS were identified as having AU. Mean gestational age was 32.5 weeks. Underlying diseases were: 5 necrotising enterocolitis, 2 gastroschisis and 1 multiple intestinal atresia. The mean age at AU diagnosis was 6.5 years (diagnosis delay of 35 months). All but 2 patients had AU persistency after medical treatment. Endoscopic treatment (2 argon plasma coagulation; 1 platelet-rich fibrin instillation; 2 endoscopic hydrostatic dilations) was effective in 3 out of 5 children. Surgery was required in 3 patients.Conclusions: Severe bowel ischemic injury, especially in preterm infant, could predispose to AU development. Medical treatment showed discouraging results. We firstly described that different endoscopic treatment could be attempted before resorting to further surgery. (c) 2017 Elsevier Inc. All rights reserved.

Fusaro, F., Tambucci, R., Romeo, E., Bagolan, P., Dall'Oglio, L., Ceccarelli, S., et al. (2018). Anastomotic ulcers in short bowel syndrome: New suggestions from a multidisciplinary approach. JOURNAL OF PEDIATRIC SURGERY, 53(3), 483-488 [10.1016/j.jpedsurg.2017.05.030].

Anastomotic ulcers in short bowel syndrome: New suggestions from a multidisciplinary approach

Bagolan P.;De Angelis P.
2018-01-01

Abstract

Background and aims: Anastomotic ulceration (AU) is a rare potential life-threatening complication that may occur after intestinal resection. The diagnosis is often delayed after a long-lasting history of refractory anemia. The pathogenesis remains unknown and there are no established therapies. The aim of the study was to analyze the medical history of children with short bowel syndrome (SBS) who were experiencing AU.Methods: Records of SBS children were retrospectively reviewed. Demographics, baseline characteristics, presentation, diagnosis and treatment of AU cases were analyzed.Results: Eight out of 114 children with SBS were identified as having AU. Mean gestational age was 32.5 weeks. Underlying diseases were: 5 necrotising enterocolitis, 2 gastroschisis and 1 multiple intestinal atresia. The mean age at AU diagnosis was 6.5 years (diagnosis delay of 35 months). All but 2 patients had AU persistency after medical treatment. Endoscopic treatment (2 argon plasma coagulation; 1 platelet-rich fibrin instillation; 2 endoscopic hydrostatic dilations) was effective in 3 out of 5 children. Surgery was required in 3 patients.Conclusions: Severe bowel ischemic injury, especially in preterm infant, could predispose to AU development. Medical treatment showed discouraging results. We firstly described that different endoscopic treatment could be attempted before resorting to further surgery. (c) 2017 Elsevier Inc. All rights reserved.
2018
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/20 - CHIRURGIA PEDIATRICA E INFANTILE
English
Short bowel syndrome
Anastomotic ulceration
Prematurity
Bowel ischemic injury
Endoscopic treatment
Fusaro, F., Tambucci, R., Romeo, E., Bagolan, P., Dall'Oglio, L., Ceccarelli, S., et al. (2018). Anastomotic ulcers in short bowel syndrome: New suggestions from a multidisciplinary approach. JOURNAL OF PEDIATRIC SURGERY, 53(3), 483-488 [10.1016/j.jpedsurg.2017.05.030].
Fusaro, F; Tambucci, R; Romeo, E; Bagolan, P; Dall'Oglio, L; Ceccarelli, S; Francalanci, P; Hermans, D; Pietrobattista, A; Diamanti, A; Torroni, F; De Angelis, P
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/274513
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