橋本病と特発性血小板減少性紫斑病に続いて悪性貧血とヘリコバクタピロリ菌感染を伴う自己免疫性胃炎を発症し， 多腺性自己免疫症候群タイプ3B と考えられた症例
Author:
Affiliation:
1. Tenri Institute of Medical Research, Tenri Hospital
2. Department of Gastroenterology, Tenri Hospital
Publisher
Tenri Foundation, Tenri Institute of Medical Research
Subject
Industrial and Manufacturing Engineering
Link
https://www.jstage.jst.go.jp/article/tenrikiyo/26/2/26_26-017/_pdf
Reference6 articles.
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2. 2. Tian S, Xu B, Liu Z, et al. Autoimmune polyglandular syndrome type III associated with antineutrophil cytoplasmic autoantibody-mediated crescentic glomerulonephritis: A case report and literature review. Medicine (Baltimore) 2020;99:e19179.
3. 3. Betterle C, Furmaniak J, Sabbadin C, et al. Type 3 autoimmune polyglandular syndrome (APS-3) or type 3 multiple autoimmune syndrome (MAS-3): an expanding galaxy. J Endocrinol Invest 2023;46:643-665.
4. 4. Means RT, Fairfield KM. Clinical manifestations and diagnosis of vitamin B12 and folate deficiency. In: Takemoto CM, Tirnauer JS, Givens J, eds. UpToDate (accessed on August 23, 2023).
5. 5. Cellini M, Santaguida MG, Virili C, et al. Hashimoto's thyroiditis and autoimmune gastritis. Front Endocrinol (Lausanne) 2017;8:92.
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