病例报告

黑斑息肉综合征伴恶变2例

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  • 长治医学院附属和平医院消化内科,山西 长治 046000

收稿日期: 2022-11-15

  网络出版日期: 2024-01-09

基金资助

国家自然科学基金项目(81600422);山西省基础研究计划项目(202303021211108)

Peutz-Jeghers syndrome with malignant transformation: 2 cases report

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Received date: 2022-11-15

  Online published: 2024-01-09

本文引用格式

霍丽丽, 王玉玮, 杨长青 . 黑斑息肉综合征伴恶变2例[J]. 内科理论与实践, 2023 , 18(04) : 287 -289 . DOI: 10.16138/j.1673-6087.2023.04.015

参考文献

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[2] van Lier MG, Wagner A, Mathus-Vliegen EM, et al. High cancer risk in Peutz-Jeghers syndrome: a systematic review and surveillance recommendations[J]. Am J Gastroenterol, 2010, 105(6): 1258-1264.
[3] Vangala DB, Cauchin E, Balma?a J, et al. Screening and surveillance in hereditary gastrointestinal cancers: recommendations from the European Society of Digestive Oncology (ESDO) expert discussion at the 20th European Society for Medical Oncology (ESMO)/World Congress on Gastrointestinal Cancer, Barcelona, June 2018[J]. Eur J Cancer, 2018, 104: 91-103.
[4] Giardiello FM, Brensinger JD, Tersmette AC, et al. Very high risk of cancer in familial Peutz-Jeghers syndrome[J]. Gastroenterology, 2000, 119(6): 1447-1453.
[5] Hearle N, Schumacher V, Menko FH, et al. Frequency and spectrum of cancers in the Peutz-Jeghers syndrome[J]. Clin Cancer Res, 2006, 12(10): 3209-3215.
[6] Resta N, Pierannunzio D, Lenato GM, et al. Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients[J]. Dig Liver Dis, 2013, 45(7): 606-611.
[7] Chen HY, Jin XW, Li BR, et al. Cancer risk in patients with Peutz-Jeghers syndrome: a retrospective cohort study of 336 cases[J]. Tumour Biol, 2017, 39(6): 1010428317705131.
[8] van Lier MG, Westerman AM, Wagner A, et al. High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome[J]. Gut, 2011, 60(2): 141-147.
[9] 中国抗癌协会家族遗传性肿瘤专业委员会. 中国家族遗传性肿瘤临床诊疗专家共识(2021年版)(4)—家族遗传性结直肠癌[J]. 中国肿瘤临床, 2022, 49(1): 1-5.
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