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甲状腺髓样癌家族性病例及相关嗜铬细胞瘤中性别分布模式的变化

Changing patterns of sex distribution in familial medullary carcinoma of the thyroid and associated phaeochromocytoma.

作者信息

Minopoli M, Bordi C

出版信息

Clin Endocrinol (Oxf). 1983 Jun;18(6):645-8. doi: 10.1111/j.1365-2265.1983.tb00603.x.

Abstract

Analysis of 49 kindreds with the familial form of medullary thyroid carcinoma (MTC) reported up to 1973 revealed a non-random sex distribution of 220 affected members, with a predominance of females among patients presenting with MTC and of males among patients presenting only with phaeochromocytoma. This pattern of sex distribution has completely disappeared among 201 patients from 47 kindreds reported in more recent years, MTC now being equally distributed between the two sexes. It is suggested that this change is related to the different diagnostic approach predominant in each period of time and that MTCs discovered at a preclinical stage by calcitonin screening are equally distributed between the sexes, while females predominate when tumours have progressed until they are clinically evident.

摘要

对截至1973年报告的49个家族性甲状腺髓样癌(MTC)家系的分析显示,220名受累成员的性别分布并非随机,MTC患者中女性占多数,仅患有嗜铬细胞瘤的患者中男性占多数。近年来报告的47个家系的201名患者中,这种性别分布模式已完全消失,现在MTC在两性之间平均分布。有人认为,这种变化与每个时期占主导地位的不同诊断方法有关,通过降钙素筛查在临床前阶段发现的MTC在两性之间平均分布,而当肿瘤进展到临床明显时女性占多数。

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