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ชื่อเรื่อง: | Prevalence of thyroid diseases in familial adenomatous polyposis: a systematic review and meta-analysis |
ผู้แต่ง: | Chenbhanich J. Atsawarungruangkit A. Korpaisarn S. Phupitakphol T. Osataphan S. Phowthongkum P. |
Keywords: | Article benign neoplasm confidence interval echography familial adenomatous polyposis human meta analysis priority journal sensitivity analysis systematic review thyroid cancer thyroid disease thyroid tumor adult age colon polyposis female genetics hyperthyroidism hypothyroidism male mutation prevalence sex factor thyroid tumor APC protein APC protein, human Adenomatous Polyposis Coli Adenomatous Polyposis Coli Protein Adult Age Factors Female Humans Hyperthyroidism Hypothyroidism Male Mutation Prevalence Sex Factors Thyroid Neoplasms |
วันที่เผยแพร่: | 2019 |
บทคัดย่อ: | Thyroid cancer (TC) is a known extra-intestinal manifestation and contributes to the mortality and morbidity in patients with familial adenomatous polyposis (FAP). Its exact prevalence is not well established and recent studies have shown an increasing number of TC in this patient population. The prevalence of benign thyroid masses and endocrinologic thyroid disorders are also poorly described. We conducted a systematic review and meta-analysis by using a random-effects model to characterize TC and estimated the prevalence of thyroid diseases in FAP patients. Twelve studies (n = 9821) were included. Pooled prevalence of TC, benign thyroid masses, and endocrinologic thyroid disorders in FAP were 2.6% [95% confidence interval (CI) 1.3–4.8], 48.8% [95% CI 33.8–64.0], and 6.9% [95% CI 4.5–10.3] respectively. Subgroup analyses revealed higher prevalence of TC in studies with fewer participants, studies that used screening ultrasound to diagnose TC, and studies that were published after 2002. TC diagnosis preceded the diagnosis of FAP in 34% of the patients. The means age at diagnosis of FAP and TC were 29 and 31 years, respectively. 95% of the patients were female and the most common pathology was of papillary subtype (83.3%). Most mutations (79.2%) were located at the 5′ end of APC gene. In summary, benign thyroid disorders are common in FAP, yet, TC is an uncommon phenomenon. Certain patient subset, such as young female with APC mutation at the 5′ end, might benefit from routine surveillance ultrasound. © 2018, Springer Science+Business Media B.V., part of Springer Nature. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/12516 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85045426434&doi=10.1007%2fs10689-018-0085-3&partnerID=40&md5=e251e6980924807128cb82d4d45297a3 |
ISSN: | 13899600 |
Appears in Collections: | Scopus 1983-2021 |
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