FAMILIAL NON-MEDULLARY THYROID CARCINOMA.

Q3 Medicine
B B Guda, I I Komisarenko, M V Ostafiichuk, M D Tronko
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引用次数: 0

Abstract

Background: Familial non-medullary thyroid carcinoma (FNMTC) is defined as cancer developing in two or more first-degree relatives if predisposing factors, for example, radiation, are absent. The disease can be either syndromic, when it is a component of complex genetic syndromes, or non-syndromic (95% cases). The genetic basis of non-syndromic FNMTC is unknown; the clinical behavior of tumorsis unclear and, at times, contradictory.

Aim: To analyze clinical manifestations of FNMTC and compare them with the data for sporadic papillary thyroid carcinomas in patients of the same age groups.

Materials and methods: We examined 22 patients (a "parents" group and a "children" group) suffering from the non-syndromic FNMTC. For comparison, two groups of sporadic papillary carcinomas patients of the same age were drawn up("adult" and "young"). We analyzed tumor size and frequency of the distributionby the categoryof TNM system, invasiveness, multifocality, metastases to lymph nodes, type and extent of surgical and radioiodine treatment, and prognosis according to the MACIS criterion.

Results: Whether sporadic or familial, the tumor size, metastatic potential, and invasive potential are higher in young people, asalready known. There was no significant difference between the "parents" and "adult" groups of patients in terms of tumor parameters. One exception was the higher frequency of multifocal tumors in the FNMTC patients. Meanwhile, compared to the "young" sporadic papillary carcinomas patients, the FNMTC "children" had a higher frequency of T2 tumors, metastasizing (N1a-N1ab), and multifocal tumors, but a lower frequency of carcinomas with intrathyroidal invasions.In the FNMTC "children" compared to FNMTC "parents" was a higher frequency of T2 tumors, metastasizing carcinomas, and tumors with capsular invasion.

Conclusion: FNMTC carcinomas are more aggressive than sporadic ones, especially in patients who are first-degree relatives in a family with parents already diagnosed with the disease.

家族性非髓样甲状腺癌。
背景:家族性非髓样甲状腺癌(FNMTC)被定义为在两个或两个以上一级亲属中发生的癌症,如果没有易感因素,例如放疗。该病既可以是综合征,当它是复杂遗传综合征的一个组成部分时,也可以是非综合征(95%病例)。非综合征性FNMTC的遗传基础尚不清楚;肿瘤的临床表现尚不清楚,有时甚至相互矛盾。目的:分析FNMTC的临床表现,并与同年龄组散发性甲状腺乳头状癌的资料进行比较。材料和方法:我们检查了22例患有非综合征性FNMTC的患者(“父母”组和“儿童”组)。为了进行比较,我们选取了两组年龄相同的散发性乳头状癌患者(“成人”和“年轻”)。我们根据TNM系统的分类、侵袭性、多灶性、淋巴结转移、手术和放射性碘治疗的类型和程度以及根据MACIS标准的预后来分析肿瘤的大小和分布频率。结果:无论是散发性还是家族性,肿瘤的大小、转移潜力和侵袭潜力在年轻人中都更高,这是已知的。“父母”组与“成人”组患者在肿瘤参数方面无显著差异。一个例外是FNMTC患者多灶性肿瘤的频率更高。同时,与“年轻”散发性乳头状癌患者相比,FNMTC“儿童”T2肿瘤、转移(N1a-N1ab)和多灶性肿瘤的发生率更高,但甲状腺内浸润癌的发生率较低。与FNMTC“父母”相比,FNMTC“孩子”发生T2肿瘤、转移性癌和囊膜浸润肿瘤的频率更高。结论:FNMTC癌的侵袭性较散发性强,尤其在父母已确诊的家庭一级亲属中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Experimental oncology
Experimental oncology Medicine-Oncology
CiteScore
1.40
自引率
0.00%
发文量
49
期刊介绍: The Experimental Oncology is an English-language journal that publishes review articles, original contributions, short communications, case reports and technical advances presenting new data in the field of experimental and fundamental oncology. Manuscripts should be written in English, contain original work, which has not been published or submitted for publication elsewhere. It also implies the transfer of the Copyright from the author to “Experimental Oncology”. No part of journal publications may be reproduced, stored in a retrieval system or transmitted in any form or by any means without the prior permission of the publisher.
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