Solitary rectal ulcer syndrome in 102 patients: Do different phenotypes make sense?


Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
ISSN: 1878-3562
Titre abrégé: Dig Liver Dis
Pays: Netherlands
ID NLM: 100958385

Informations de publication

Date de publication:
02 2021
Historique:
received: 06 09 2020
revised: 30 10 2020
accepted: 31 10 2020
pubmed: 18 11 2020
medline: 15 12 2021
entrez: 17 11 2020
Statut: ppublish

Résumé

Little is known about the pathophysiological mechanisms of solitary rectal ulcer syndrome (SRUS). We aim to identify the different phenotypes, taking into account complaints, anatomy and anorectal physiology. Complaints, endoscopy results, and physiology data of patients with histologically proven SRUS were collected and analysed. The associated anorectal diseases were faecal incontinence and obstructed defecation. The clinical aspects of SRUS were compared, and factors associated with anorectal diseases were identified. Overall, 102 consecutive patients were included. The predominant lesion was a rectal ulcer (66%), and inflammation of the rectal wall was present in 42% of patients. Abnormal rectal capacities and/or rectal perception was observed in more than half. Nearly half (52%) of the patients met the criteria for obstructed defecation and they tended to more frequently have psychiatric disease (66.7% vs 33.3%; p=0.07). Patients with faecal incontinence (17%) reported more self-perception of anal procidentia (p=0.01) and were more likely to have inflammation of the rectal wall (p=0.02), high-grade internal rectal procidentia (p=0.06) and anal hypotonia (p=0.004); their maximum tolerable volume was lower (p=0.004). The characteristics of patients with SRUS suggest different phenotypes. This may be a way to develop a comprehensive treatment strategy.

Sections du résumé

BACKGROUND
Little is known about the pathophysiological mechanisms of solitary rectal ulcer syndrome (SRUS).
AIMS
We aim to identify the different phenotypes, taking into account complaints, anatomy and anorectal physiology.
METHODS
Complaints, endoscopy results, and physiology data of patients with histologically proven SRUS were collected and analysed. The associated anorectal diseases were faecal incontinence and obstructed defecation. The clinical aspects of SRUS were compared, and factors associated with anorectal diseases were identified.
RESULTS
Overall, 102 consecutive patients were included. The predominant lesion was a rectal ulcer (66%), and inflammation of the rectal wall was present in 42% of patients. Abnormal rectal capacities and/or rectal perception was observed in more than half. Nearly half (52%) of the patients met the criteria for obstructed defecation and they tended to more frequently have psychiatric disease (66.7% vs 33.3%; p=0.07). Patients with faecal incontinence (17%) reported more self-perception of anal procidentia (p=0.01) and were more likely to have inflammation of the rectal wall (p=0.02), high-grade internal rectal procidentia (p=0.06) and anal hypotonia (p=0.004); their maximum tolerable volume was lower (p=0.004).
CONCLUSION
The characteristics of patients with SRUS suggest different phenotypes. This may be a way to develop a comprehensive treatment strategy.

Identifiants

pubmed: 33199231
pii: S1590-8658(20)30995-6
doi: 10.1016/j.dld.2020.10.041
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

190-195

Informations de copyright

Copyright © 2020 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Claire Gouriou (C)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France.

Laurent Siproudhis (L)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France; CIC 1414, INPHY, Université de Rennes 1, Rennes, France; INSERM U1241, Université de Rennes 1, Rennes, France.

Marion Chambaz (M)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France; Service d'Explorations Fonctionnelles Digestives, CHU Pontchaillou, Université de Rennes 1, Rennes, France.

Alain Ropert (A)

CIC 1414, INPHY, Université de Rennes 1, Rennes, France; Service d'Explorations Fonctionnelles Digestives, CHU Pontchaillou, Université de Rennes 1, Rennes, France.

Timothée Wallenhorst (T)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France.

Alexandre Merlini-l'Héritier (A)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France.

Aurore Carlo (A)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France.

Guillaume Bouguen (G)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France; CIC 1414, INPHY, Université de Rennes 1, Rennes, France; INSERM U1241, Université de Rennes 1, Rennes, France.

Charlène Brochard (C)

Service des Maladies de l'Appareil Digestif, CHU Pontchaillou, Université de Rennes 1, 2 rue Henri le Guillou, 35033 Rennes Cedex, France; CIC 1414, INPHY, Université de Rennes 1, Rennes, France; Service d'Explorations Fonctionnelles Digestives, CHU Pontchaillou, Université de Rennes 1, Rennes, France. Electronic address: charlene.brochard@chu-rennes.fr.

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