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Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies

We herein report a case of granulomatosis with polyangiitis in a 73-year-old man. He had experienced bilateral ptosis, redness of both eyes, right facial weakness, and hearing loss in the right ear for two months. Myeloperoxidase anti-neutrophil cytoplasmic antibody was positive. Corticosteroids and...

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Autores principales: Horiuchi, Kazuhiro, Oshima, Yuki, Kudo, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079918/
https://www.ncbi.nlm.nih.gov/pubmed/33132328
http://dx.doi.org/10.2169/internalmedicine.4881-20
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author Horiuchi, Kazuhiro
Oshima, Yuki
Kudo, Akihiko
author_facet Horiuchi, Kazuhiro
Oshima, Yuki
Kudo, Akihiko
author_sort Horiuchi, Kazuhiro
collection PubMed
description We herein report a case of granulomatosis with polyangiitis in a 73-year-old man. He had experienced bilateral ptosis, redness of both eyes, right facial weakness, and hearing loss in the right ear for two months. Myeloperoxidase anti-neutrophil cytoplasmic antibody was positive. Corticosteroids and intravenous cyclophosphamide pulse therapy yielded a response. After the fourth pulse of cyclophosphamide, he developed headache, diplopia, restricted left eye movement, right facial palsy, and hearing loss in the right ear. A one-year remission period was achieved by increasing the steroid and rituximab doses. Rituximab was effective against the relapse of granulomatosis with polyangiitis and cranial neuropathy.
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spelling pubmed-80799182021-05-11 Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies Horiuchi, Kazuhiro Oshima, Yuki Kudo, Akihiko Intern Med Case Report We herein report a case of granulomatosis with polyangiitis in a 73-year-old man. He had experienced bilateral ptosis, redness of both eyes, right facial weakness, and hearing loss in the right ear for two months. Myeloperoxidase anti-neutrophil cytoplasmic antibody was positive. Corticosteroids and intravenous cyclophosphamide pulse therapy yielded a response. After the fourth pulse of cyclophosphamide, he developed headache, diplopia, restricted left eye movement, right facial palsy, and hearing loss in the right ear. A one-year remission period was achieved by increasing the steroid and rituximab doses. Rituximab was effective against the relapse of granulomatosis with polyangiitis and cranial neuropathy. The Japanese Society of Internal Medicine 2020-11-02 2021-04-01 /pmc/articles/PMC8079918/ /pubmed/33132328 http://dx.doi.org/10.2169/internalmedicine.4881-20 Text en Copyright © 2021 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Horiuchi, Kazuhiro
Oshima, Yuki
Kudo, Akihiko
Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies
title Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies
title_full Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies
title_fullStr Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies
title_full_unstemmed Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies
title_short Successful Treatment with Rituximab for Granulomatosis with Polyangiitis and Multiple Cranial Neuropathies
title_sort successful treatment with rituximab for granulomatosis with polyangiitis and multiple cranial neuropathies
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079918/
https://www.ncbi.nlm.nih.gov/pubmed/33132328
http://dx.doi.org/10.2169/internalmedicine.4881-20
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