12
views
0
recommends
+1 Recommend
2 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      COVID–19ワクチン接種後に副腎クリーゼ,たこつぼ心筋症を発症しショックとなり多腺性自己免疫症候群2型の診断に至った1例(A patient with post COVID–19 vaccination presented with convulsions and cardiogenic shock due to adrenal crisis and Takotsubo cardiomyopathy diagnosed with autoimmune polyendocrine syndromes type II and Addison’s disease)

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          A 49–year–old woman with a history of Basedow’s disease and vitiligo during her 30s was presented with 5 days of dizziness, nausea, and fatigue after being administered the third COVID–19 vaccination and transported via emergency medical service to the emergency department with sudden loss of consciousness and convulsions. Head and whole body computed tomography were normal but laboratory examination showed severe hyponatremia, which could be the cause of severe consciousness disturbance. Similar to what is observed in Takotsubo cardiomyopathy, echocardiography revealed a mid–ventricular and apical heart–wall motion, appearing as hypokinesis; in contrast, the basal segment showed preserved features. The left ventricular dysfunction caused the progressive hypotension and cardiogenic shock. Empiric treatment with corticosteroid considering the adrenal insufficiency, mechanical circulatory support with intra–aortic balloon pumping, and proper correction of hyponatremia were effective. The patient was extubated by day 7, leading to full recovery. Additional tests confirmed the diagnosis of autoimmune polyendocrine syndromes type II (Schmidt syndrome) and Addison’s disease. This case shows that adrenal crisis is caused by the vaccine’s stress and autoimmune reaction in specific individuals. Since it is an acute life–threatening emergency, early identification and prompt management is essential.

          要旨

          若年時にバセドウ病,白斑病の既往のある49歳女性。COVID–19ワクチン接種後からめまい,嘔気,体動困難が出現し,5日後に意識障害,心原性ショック状態で救急搬送された。低ナトリウム血症に伴う重症意識障害,たこつぼ心筋症の診断で,挿管人工呼吸管理,電解質補正,大動脈バルーンパンピングを含む心不全治療を開始した。副腎不全を鑑別に直ちにステロイド補充を開始したところ全身状態は改善傾向となり,第7病日に抜管した。状態回復後の内分泌機能精査で,原発性副腎機能不全,多腺性自己免疫症候群2型の診断に至った。副腎クリーゼは初発だと診断がつきづらいが,重症意識障害やたこつぼ心筋症を合併し致命的となりうる重症病態であり,早期ステロイド補充が救命に不可欠である。今回,COVID–19ワクチン接種を契機に初発の副腎クリーゼを発症したが,集学的治療を行い救命しえた多腺性自己免疫症候群2型の1例を経験したため報告する。

          Related collections

          Most cited references10

          • Record: found
          • Abstract: not found
          • Article: not found

          Autoimmune Polyendocrine Syndromes

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Acute autoimmune-like hepatitis with atypical anti-mitochondrial antibody after mRNA COVID-19 vaccination: A novel clinical entity?

            Autoimmune phenomena and clinically apparent autoimmune diseases, including autoimmune hepatitis, are increasingly been reported not only after natural infection with the SARS-CoV-2 virus, but also after vaccination against it. We report the case of a 63-year old man without a history of autoimmunity or SARS-CoV-2 natural infection who experienced acute severe autoimmune-like hepatitis seven days after the first dose of the mRNA-1273 SARS-CoV-2 vaccine. Liver histology showed inflammatory portal infiltrate with interface hepatitis, lobular and centrilobular inflammation with centrilobular necrosis, in absence of fibrosis and steatosis. Serum immunoglobulin G was slightly elevated. Autoimmune liver serology showed an indirect immunofluorescence pattern on triple rodent tissue compatible with anti-mitochondrial antibody (AMA), but, unexpectedly, this pattern was not mirrored by positivity for primary biliary cholangitis (PBC)-specific molecular tests, indicating that this antibody is different from classical AMA. Anti-nuclear antibody (ANA) was also positive with a rim-like indirect immunofluorescence pattern on liver and HEp2 cell substrates, similar to PBC-specific ANA; however, anti-gp210 and a large panel of molecular-based assays for nuclear antigens were negative, suggesting a unique ANA in our patient. He carries the HLA DRB1*11:01 allele, which is protective against PBC. Response to prednisone treatment was satisfactory. The clinical significance of these novel specificities needs to be further evaluated in this emerging condition.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Polyglandular autoimmune syndromes.

              In recent years, scientific knowledge pertaining to the rare ORPHAN polyglandular autoimmune syndrome (registered code ORPHA 282196) has accumulated.
                Bookmark

                Author and article information

                Contributors
                kuge-tmd@umin.org
                Journal
                10.1002/(ISSN)1883-3772
                JJA2
                Nihon Kyukyu Igakkai Zasshi
                John Wiley and Sons Inc. (Hoboken )
                0915-924X
                1883-3772
                30 November 2022
                December 2022
                30 November 2022
                : 33
                : 12 ( doiID: 10.1002/jja2.2022.v33.12 )
                : 1016-1021
                Affiliations
                [ 1 ] 東京医科歯科大学病院救命救急センター(Trauma and Acute Critical Care Center, Tokyo Medical and Dental University Hospital)
                [ 2 ] 東京医科歯科大学病院糖尿病・内分泌・代謝内科(Department of Molecular Endocrinology and Metabolism, Tokyo Medical and Dental University Hospital)
                Author notes
                [*] [* ] 〒113-8519 東京都文京区湯島1-5-45 東京医科歯科大学病院救命救急センター

                Article
                JJA212750
                10.1002/jja2.12750
                9877992
                c92b0b1a-1380-49a5-8a02-52f2352e34c3
                ©2022. Japanese Association for Acute Medicine. All Rights Reserved.

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 19 August 2022
                Page count
                Figures: 3, Tables: 1, Pages: 6, Words: 9127
                Categories
                Case Report
                Case Report
                Custom metadata
                2.0
                December 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.4 mode:remove_FC converted:26.01.2023

                basedow’s disease,adrenal insufficiency,steroid therapy

                Comments

                Comment on this article