多发性内分泌肿瘤2型早期精准诊治策略  被引量:3

The trends in early precision diagnosis and treatment strategies of multiple endocrine neoplasia type 2

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作  者:戚晓平 金百冶[2] Qi Xiaoping;Jin Baiye(Department of Oncologic and Urologic Surgery,the 903rd Hospital of People′s Liberation Army,Hangzhou Medical College,Hangzhou 310004,China;Department of Urology,the First Affiliated Hospital,School of Medicine,Zhejiang University School of Medicine,Hangzhou 311200,China)

机构地区:[1]杭州医学院联勤保障部队第九〇三医院肿瘤泌尿外科,杭州310004 [2]浙江大学医学院附属第一医院泌尿外科,杭州311200

出  处:《中华外科杂志》2022年第11期973-980,共8页Chinese Journal of Surgery

基  金:国家自然科学基金(81472861);浙江省重大科技专项(2014C03048-1);杭州市卫生科技计划(B20210355,OO20190253)。

摘  要:多发性内分泌肿瘤2型(MEN2)是一种常染色体显性遗传的神经内分泌癌症综合征,临床特征性表现为甲状腺髓样癌,伴或不伴嗜铬细胞瘤、甲状旁腺功能亢进和内分泌腺外表型;有2种亚型MEN2A和MEN2B。基于RET突变与MEN2表型的相关性,通过产前诊断和植入前基因检测,可预防(preventive)MEN2发生;整合RET突变和血清降钙素等检测,可准确预测(predictive)MEN2进展,进而实施MEN2的个性化(personalized)精准治疗。此外,着力提高对MEN2的认识,需医务人员、患者和家属,以及相关组织机构的共同参与(participation),并辅以心理支持(psychological support),可促进MEN2的综合诊治水平的全面提高。MEN2的"5P诊治策略"是精确医学的范例代表,可有效避免或减少MEN2的临床危害,改善MEN2患者预后及其生活质量。Multiple endocrine neoplasia type 2(MEN2)is an autosomal dominant hereditary neuroendocrine cancer syndrome characterized by medullary thyroid carcinoma,in combination or not with pheochromocytoma,hyperparathyroidism and extra-endocrine features,and two forms subtyped as MEN2A and MEN2B.Based on the correlation between RET proto-oncogene mutation and MEN2 phenotype,MEN2 could be prevented through prenatal diagnosis and preimplantation genetic testing.Integrating the detection of RET mutation with measurement of serum calcitonin,plasma or urinary metanephrine/normetanephrine,and serum parathyroid hormone levels could accurately predict the progression of MEN2,and then facilitating implementation of personalized precision treatment.In addition,increased awareness of MEN2 is needed,which requires participation of physicians,patients/family members,and relevant organizations,supplemented by psychological support,which could promote the comprehensive management of MEN2.The"5P"strategies for MEN2 represents a paradigm of precision medicine,which could effectively avoid or reduce the clinical adverse outcomes,improve the prognosis and quality of life of MEN2 patients.

关 键 词:多发性内分泌瘤病 早期诊断 甲状腺髓样癌 嗜铬细胞瘤 RET原癌基因 遗传学诊断 精准医学 

分 类 号:R736[医药卫生—肿瘤]

 

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