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Cerebellar infarction as the initial presentation of IgG4‐related disease

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. Steroi...

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Autores principales: Ireifej, Branden, Dhamrah, Umaima, Song, David, Bitar, Joyce, Jaiswal, Vikash, Nepal, Gaurav, Pathak, Nibesh, Freijat, Majd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931459/
https://www.ncbi.nlm.nih.gov/pubmed/35340659
http://dx.doi.org/10.1002/ccr3.5614
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author Ireifej, Branden
Dhamrah, Umaima
Song, David
Bitar, Joyce
Jaiswal, Vikash
Nepal, Gaurav
Pathak, Nibesh
Freijat, Majd
author_facet Ireifej, Branden
Dhamrah, Umaima
Song, David
Bitar, Joyce
Jaiswal, Vikash
Nepal, Gaurav
Pathak, Nibesh
Freijat, Majd
author_sort Ireifej, Branden
collection PubMed
description 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.
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spelling pubmed-89314592022-03-24 Cerebellar infarction as the initial presentation of IgG4‐related disease Ireifej, Branden Dhamrah, Umaima Song, David Bitar, Joyce Jaiswal, Vikash Nepal, Gaurav Pathak, Nibesh Freijat, Majd Clin Case Rep Case Reports 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. John Wiley and Sons Inc. 2022-03-17 /pmc/articles/PMC8931459/ /pubmed/35340659 http://dx.doi.org/10.1002/ccr3.5614 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Ireifej, Branden
Dhamrah, Umaima
Song, David
Bitar, Joyce
Jaiswal, Vikash
Nepal, Gaurav
Pathak, Nibesh
Freijat, Majd
Cerebellar infarction as the initial presentation of IgG4‐related disease
title Cerebellar infarction as the initial presentation of IgG4‐related disease
title_full Cerebellar infarction as the initial presentation of IgG4‐related disease
title_fullStr Cerebellar infarction as the initial presentation of IgG4‐related disease
title_full_unstemmed Cerebellar infarction as the initial presentation of IgG4‐related disease
title_short Cerebellar infarction as the initial presentation of IgG4‐related disease
title_sort cerebellar infarction as the initial presentation of igg4‐related disease
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931459/
https://www.ncbi.nlm.nih.gov/pubmed/35340659
http://dx.doi.org/10.1002/ccr3.5614
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