Cerebellar infarction as the initial presentation of IgG4-related disease.
CNS
IgG4‐RD
cerebellum
lymphoplasmacytic
plasma cells
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Mar 2022
Mar 2022
Historique:
received:
05
02
2022
revised:
08
03
2022
accepted:
09
03
2022
entrez:
28
3
2022
pubmed:
29
3
2022
medline:
29
3
2022
Statut:
epublish
Résumé
Although IgG4-RD has CNS manifestations, cerebellar involvement has only been reported in three cases. Our patient presented with cerebellar symptoms, several cerebellar infarcts were evident on the brain MRI, and CT abdomen revealed retroperitoneal tumor. Endoscopic biopsy confirmed IgG4-RD. Steroids are the first-line therapy for IgG4-RD, but our patient was lost to follow-up before treatment.
Identifiants
pubmed: 35340659
doi: 10.1002/ccr3.5614
pii: CCR35614
pmc: PMC8931459
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e05614Informations de copyright
© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
The authors declare that they have no conflicts of interest to declare.
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