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dc.contributor.authorMitani, Kokien
dc.contributor.authorFunaki, Takeshien
dc.contributor.authorTanji, Masahiroen
dc.contributor.authorOnizawa, Hideoen
dc.contributor.authorYoshifuji, Hajimeen
dc.contributor.authorFushimi, Yasutakaen
dc.contributor.authorTorimaki, Shinyaen
dc.contributor.authorYoshida, Kazumichien
dc.contributor.authorMiyamoto, Susumuen
dc.contributor.alternative三谷, 幸輝ja
dc.contributor.alternative舟木, 健史ja
dc.contributor.alternative丹治, 正大ja
dc.contributor.alternative鬼澤, 秀夫ja
dc.contributor.alternative吉藤, 元ja
dc.contributor.alternative伏見, 育崇ja
dc.contributor.alternative鳥牧, 伸哉ja
dc.contributor.alternative吉田, 和道ja
dc.contributor.alternative宮本, 享ja
dc.date.accessioned2023-07-10T05:53:05Z-
dc.date.available2023-07-10T05:53:05Z-
dc.date.issued2022-
dc.identifier.urihttp://hdl.handle.net/2433/284034-
dc.description.abstract[Background] Detecting immunoglobulin G4 (IgG4)-related intracranial arteriopathy, a rare neurovascular complication of IgG4-related disease, is challenging. While magnetic resonance (MR) vessel wall imaging (VWI) can visualize various neurovascular pathologies, its application to this arteriopathy has not been reported as of this writing. [Case presentation] A 74-year-old male and a 65-year-old female manifested multiple cranial nerve palsy and neck pain, respectively. Both cases exhibited multiorgan masses with markedly elevated serum IgG4 levels and were clinically diagnosed with IgG4-related disease. Three-dimensional T1-weighted black blood VWI with and without contrast agent identified intracranial vascular lesions characterized as nearly-circumferential mural thickening with homogeneous contrast enhancement in the internal carotid and vertebral arteries; some of the lesions had been unrecognized with screening MR angiography due to expansive remodeling. The former patient underwent corticosteroid therapy, and VWI after treatment revealed decreased mural thickening and enhancement. [Conclusion] Further studies to elucidate characteristic findings of VWI might contribute to early detection of this treatable pathology.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.publisherBMCen
dc.rights© The Author(s) 2022en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectCNS vasculitisen
dc.subjectIgG4-related diseaseen
dc.subjectMagnetic resonance imagingen
dc.subjectVessel wall imagingen
dc.subjectDANTEen
dc.subjectCase reporten
dc.titleDetecting immunoglobulin G4-related intracranial arteriopathy with magnetic resonance vessel wall imaging: a preliminary experience in two casesen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleBMC Neurologyen
dc.identifier.volume22-
dc.relation.doi10.1186/s12883-022-03010-8-
dc.textversionpublisher-
dc.identifier.artnum476-
dc.identifier.pmid36510148-
dcterms.accessRightsopen access-
dc.identifier.eissn1471-2377-
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