甲状腺碰撞瘤。一种特殊的临床和病理实体

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Archive of clinical cases Pub Date : 2021-12-29 eCollection Date: 2021-01-01 DOI:10.22551/2021.33.0804.10191
Andreea Bojoga, Laura Stănescu, Corin Badiu
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引用次数: 8

摘要

甲状腺碰撞瘤是指两个组织学和形态学上不同的肿瘤同时发生或从甲状腺内其他器官转移而来的罕见肿瘤。髓样癌与乳头状癌共发最为常见。几种理论试图解释碰撞肿瘤的致病机制,包括假设一种肿瘤易致另一种肿瘤的理论、干细胞理论和随机效应理论,但它们的结合更好地解释了这些肿瘤的起源。对其发病机制的共同遗传行为也提出了假说,如RET (rearrange during Transfection)原癌基因的种系突变参与了甲状腺髓样癌和甲状腺乳头状癌的共存,但这一话题存在争议。由于两种不同的肿瘤具有不同的生物侵袭性、治疗选择和预后,需要个体化治疗,甲状腺碰撞瘤的治疗具有挑战性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Collision tumors of the thyroid. A special clinical and pathological entity.

Thyroid collision tumors are rare entities that designate two histologically and morphologically distinct tumors that occur simultaneously or as metastases from other organs within the thyroid. Medullary and papillary carcinoma co-occurrence is the most frequent. Several theories tried to explain the pathogenic mechanisms underlining collision tumors, including the theory which assumes that one tumor predisposes the other, stem cell theory, and random effect theory, but their combination better explains the origin of these tumors. Hypotheses about common genetic behavior responsible for the pathogenesis have also been suggested, such as the involvement of germline mutation of RET (Rearranged during Transfection) proto-oncogene in medullary thyroid carcinoma and papillary thyroid carcinoma coexistence, but there is controversy on this topic. Management of thyroid collision tumors is challenging owing to the presence of two distinct tumors with different biological aggressiveness, treatments options, and prognosis, and needs to be individualized.

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