Recurrent Henoch Schönlein purpura without renal involvement successfully treated with methotrexate.
Child
Henoch-Schönlein purpura
IgA vasculitis
methotrexate
recurrence
Journal
Scottish medical journal
ISSN: 0036-9330
Titre abrégé: Scott Med J
Pays: Scotland
ID NLM: 2983335R
Informations de publication
Date de publication:
May 2019
May 2019
Historique:
pubmed:
21
11
2018
medline:
24
12
2019
entrez:
21
11
2018
Statut:
ppublish
Résumé
Henoch Schönlein purpura is characterised by palpable purpura, abdominal pain, arthritis/arthralgia, often with a self-limiting course. Herein, we report a patient with recurrent Henoch Schönlein purpura and severe gastrointestinal involvement, successfully treated with methotrexate. A 12-year-old boy was admitted to our department with palpable purpura, abdominal pain and arthralgia. Since gastrointestinal complaints were severe, systemic steroids were administered, with tapering of dosage. Henoch Schönlein purpura recurred several times with severe abdominal pain, maelena and purpura during next two months. Colchicine and hydroxychloroquine were initiated. After four months, we also introduced methotrexate, which enabled discontinuation of previous medications including corticosteroids. Methotrexate was ceased four months later, and remission was sustained without any medications for 24 months. Besides the conflicting data regarding the use of methotrexate in recurrent Henoch Schönlein purpura, our case introduces successful methotrexate experience in a child with Henoch Schönlein purpura and recurrent severe gastrointestinal involvement.
Identifiants
pubmed: 30453828
doi: 10.1177/0036933018809816
doi:
Substances chimiques
Immunosuppressive Agents
0
Methotrexate
YL5FZ2Y5U1
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM