Literature DB >> 24347288

Total colonic aganglionosis: a 15-year single center experience.

Simon Blackburn1, Phillip Corbett1, D Mervyn Griffiths1, David Burge1, R Mark Beattie2, Michael Stanton1.   

Abstract

PURPOSE: Total colonic aganglionosis (TCA) is a rare condition, which is challenging to manage. Outcome data are sparse. We aimed to review the demographics, treatment, and outcomes of TCA in our center. PATIENTS AND METHODS: A retrospective case note review of 15 years from a single center was undertaken.
RESULTS: A total of nine patients (five male) were managed. Gestational age at birth was 39 weeks (range, 32.5-41 weeks). All patients were referred with distal intestinal obstruction at a median of day 2 (range, 1-6 days) of life. Two patients were managed with a long-term stoma. One died with persistent functional obstruction (despite a ganglionic stoma). Of the nine patients, seven patients underwent staged pull-through: three Soave, three Duhamel, and one Martin procedure with no short-term complications. All patients had at least one readmission with enterocolitis, diarrhea, or high stoma output. Further procedures were required in four of the seven patients. Only one child (older than 3 years) has achieved continence. Two children (both aged 8 years) requested reformation of a stoma to manage incontinence.
CONCLUSION: In this series, we observed high morbidity and poor functional outcome, which should be anticipated in TCA. Patients with TCA have a high probability of requiring a long-term stoma and this should be considered as a management option. Georg Thieme Verlag KG Stuttgart · New York.

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Mesh:

Year:  2013        PMID: 24347288     DOI: 10.1055/s-0033-1363159

Source DB:  PubMed          Journal:  Eur J Pediatr Surg        ISSN: 0939-7248            Impact factor:   2.191


  5 in total

1.  Long-term results of total colonic agangliosis patients treated by preservation of the aganglionic right hemicolon and the ileo-cecal valve.

Authors:  Eva E Amerstorfer; Günter Fasching; Holger Till; Andrea Huber-Zeyringer; Michael E Höllwarth
Journal:  Pediatr Surg Int       Date:  2015-07-10       Impact factor: 1.827

2.  Hirschsprung's disease - Postsurgical intestinal dysmotility.

Authors:  Mariana Tresoldi das Neves Romaneli; Antonio Fernando Ribeiro; Joaquim Murray Bustorff-Silva; Rita Barbosa de Carvalho; Elizete Aparecida Lomazi
Journal:  Rev Paul Pediatr       Date:  2016-02-18

Review 3.  Hirschsprung Disease beyond Infancy.

Authors:  Casey M Calkins
Journal:  Clin Colon Rectal Surg       Date:  2018-02-25

4.  Atypical onset of total colonic Hirschsprung disease in a small female infant: A case report.

Authors:  Cristina Oana Mărginean; Lorena Elena Meliţ; Horea Gozar; Emoke Horvath; Cristian Dan Mărginean
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

5.  Minimizing Enterostomy Complication in Neonates, Lessons Learnt from Three European Tertiary Centres.

Authors:  Riccardo Coletta; Andrea Zulli; Kathryn O'Shea; Elisa Mussi; Adrian Bianchi; Antonino Morabito
Journal:  Children (Basel)       Date:  2022-01-27
  5 in total

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