Incidence of medullary thyroid carcinoma and Hirschsprung disease based on the cosmos database

医学 甲状腺癌 多发性内分泌肿瘤 入射(几何) 多发性内分泌肿瘤2型 人口 胃肠病学 内科学 甲状腺髓样癌 嗜铬细胞瘤 疾病 髓腔 甲状腺 种系突变 突变 生物化学 化学 物理 环境卫生 光学 基因
作者
Lea A. Wehrli,Marina L. Reppucci,Julia Ketzer,Alfredo Dominguez-Muñoz,Edward H. Cooper,Alberto Peña,Andrea Bischoff,Luis de la Torre
出处
期刊:Pediatric Surgery International [Springer Science+Business Media]
卷期号:39 (1)
标识
DOI:10.1007/s00383-023-05511-0
摘要

Multiple endocrine neoplasia Type 2A (MEN2A) can occur with Hirschsprung disease (HD) due to mutation in the RET proto-oncogene, with the majority developing medullary thyroid carcinoma (MTC). Given the comorbidity, many parents have contacted us to share concerns and unfortunate experiences about the prevalence rates of MEN2A/MTC in patients with HD. The aim is to determine the prevalence rate of patients with HD and MEN2A or medullary thyroid carcinoma, respectively. This is a cross-sectional study of the COSMOS database from January 01, 2017, to March 08, 2023. The database was searched for patients diagnosed with MEN2A, MTC, and HD. IRB exemption was provided (COMIRB #23-0526). The database contained 183,993,122 patients from 198 contributing organizations. The prevalence of HD and MEN2A was 0.00002%, and for HD and MTC was 0.000009%. One in 66 patients (1.5%) with MEN2A also had HD. One in 319 patients (0.3%) in the HD group had MEN2A. One in 839 patients (0.1%) within the HD population had MTC. The prevalence of MTC and HD or MEN2A and HD in the study population was low. Considering that almost all MEN2A patients have a positive family history, this data does not support the general genetic testing of HD patients.
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