Juvenile Gastric Gastrointestinal Stromal Tumor with Lymph Node Metastasis: A Case Report
Author:
Affiliation:
1. Department of Gastroenterological Surgery, Osaka University Graduate School of Medicine
2. Department of Pathology, Osaka University Graduate School of Medicine
Publisher
The Japanese Journal of Gastroenterological Surgery
Subject
Gastroenterology,Surgery
Link
https://www.jstage.jst.go.jp/article/jjgs/55/1/55_2020.0196/_pdf
Reference18 articles.
1. 1) 一般社団法人日本消化器外科学会 消化器外科専門医テキスト制作委員会編.消化器外科専門医の心得 2020年度版 上巻.東京:一般社団法人日本消化器外科学会;2020. p. 389–393.
2. 2) Miettinen M, Lasota J, Sobin HL. Gastrointestinal stromal tumors of the stomach in children and young adults: a clinicopathologic, immunohistochemical, and molecular genetic study of 44 cases with long-term follow-up and review of the literature. Am J Surg Pathol. 2005 Oct;29(10):1373–1381.
3. 4) Wada R, Arai H, Kure S, Peng W, Naito Z. “Wild type” GIST: Clinicopathological features and clinical practice. Pathol Int. 2016 Aug;66(8):431–437.
4. 5) Janeway AK, Kim SY, Lodish M, Nosé V, Rustin P, Gaal J, et al. Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations. Proc Natl Acad Sci U S A. 2011 Jan;108(1):314–318.
5. 6) Settas N, Faucz RF, Stratakis AC. Succinate dehydrogenase (SDH) deficiency, Carney triad and the epigenome. Mol Cell Endocrinol. 2018 Jul;469:107–111.
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