Severe Abdominal Manifestations in Juvenile Dermatomyositis.


Journal

Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
Titre abrégé: J Pediatr Gastroenterol Nutr
Pays: United States
ID NLM: 8211545

Informations de publication

Date de publication:
02 2020
Historique:
entrez: 25 1 2020
pubmed: 25 1 2020
medline: 22 6 2021
Statut: ppublish

Résumé

Juvenile dermatomyositis (JDM) is a rare and heterogeneous pediatric-onset idiopathic inflammatory myopathy. Gastrointestinal (GI) involvement occurs in 22% to 37% of JDM patients but has only been described in case reports. In this retrospective, single-center, observational study, we aimed to assess the causes and management of severe GI manifestations in JDM patients. We studied a cohort of 9 patients among 110 JDM patients followed during the study period (8.3%). The GI complications were related to JDM in most cases (17/19), with digestive tract involvement (n = 10), acute pancreatitis (n = 4), and hepatitis (n = 3). Three patients died from refractory JDM 2.9 years (2-3.6) after the JDM diagnosis. We highlight the need to consider pancreatitis as a main diagnostic factor in JDM patients with severe GI manifestations and the requirement of early aggressive treatment for these patients.

Identifiants

pubmed: 31978027
doi: 10.1097/MPG.0000000000002575
pii: 00005176-202002000-00023
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

247-251

Références

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Auteurs

Caroline Besnard (C)

Laboratoire d'Immunogénétique des maladies auto-immunes de l'enfant, Institut Imagine, INSERM U 1163.

Cyril Gitiaux (C)

Université de Paris.
Service de Neurophysiologie clinique, Centre de Référence des Maladies Neuromusculaires.

Muriel Girard (M)

Université de Paris.
Service de Gastroentérologie et d'Hépatologie pédiatrique.
UF d'Hépatologie pédiatrique, Centre National de Référence Maladies Rares AVB-Cholestases génétiques, Hôpital Necker, APHP.
Equipe Contrôle de la croissance cellulaire par les nutriments, Institut Necker Enfants-Malades, INSERM U1151.

Louise Galmiche-Rolland (L)

Service d'anatomo-pathologie.

Cécile Talbotec (C)

Service de Gastroentérologie et d'Hépatologie pédiatrique.

Pierre Quartier (P)

Laboratoire d'Immunogénétique des maladies auto-immunes de l'enfant, Institut Imagine, INSERM U 1163.
Université de Paris.
Service d'Immunologie, Hématologie et Rhumatologie pédiatrique, centre de référence national des maladies rhumatologiques et systémiques auto-immunes rares pédiatriques (RAISE).

Christine Bodemer (C)

Université de Paris.
Service de Dermatologie et Dermatologie Pédiatrique.

Laureline Berteloot (L)

Service d'Imagerie Pédiatrique, Hôpital Necker, APHP, Paris, France.

Brigitte Bader-Meunier (B)

Laboratoire d'Immunogénétique des maladies auto-immunes de l'enfant, Institut Imagine, INSERM U 1163.
Service d'Immunologie, Hématologie et Rhumatologie pédiatrique, centre de référence national des maladies rhumatologiques et systémiques auto-immunes rares pédiatriques (RAISE).

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Classifications MeSH