University of Missouri School of Medicine, Columbia, USA.
Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA, 02115, USA.
Head Neck Pathol. 2022 Mar;16(1):190-199. doi: 10.1007/s12105-022-01417-w. Epub 2022 Mar 21.
DICER1 syndrome is an autosomal dominant tumor predisposition syndrome caused by germline DICER1 mutations. In the thyroid, DICER1 syndrome is associated with early-onset multinodular goiter and thyroid carcinomas. Subsequent studies have shown that somatic DICER1 mutations, though rare, can occur in follicular-patterned thyroid tumors, such as follicular adenomas and follicular thyroid carcinomas, with a higher rate seen in pediatric follicular thyroid carcinomas and in follicular thyroid carcinomas with a macrofollicular architecture. Somatic DICER1 mutations have also been reported in pediatric papillary thyroid carcinomas lacking other alterations typically associated with thyroid tumorigenesis. Although thyroid carcinomas with underlying DICER1 mutations are usually indolent, recent studies have shown that pediatric poorly differentiated thyroid carcinoma and thyroblastoma, both aggressive tumors, also harbor DICER1 mutations. This review will discuss mechanisms of DICER1 tumorigenesis and describe thyroid tumors associated with germline and somatic DICER1 mutations.
DICER1 综合征是一种常染色体显性遗传肿瘤易感性综合征,由种系 DICER1 突变引起。在甲状腺中,DICER1 综合征与早发性多结节性甲状腺肿和甲状腺癌有关。随后的研究表明,体细胞 DICER1 突变虽然罕见,但可发生于滤泡模式的甲状腺肿瘤中,如滤泡性腺瘤和滤泡性甲状腺癌,在儿科滤泡性甲状腺癌和具有大滤泡结构的滤泡性甲状腺癌中更为常见。体细胞 DICER1 突变也已在缺乏与甲状腺肿瘤发生相关的其他改变的儿科乳头状甲状腺癌中报道。尽管具有潜在 DICER1 突变的甲状腺癌通常惰性,但最近的研究表明,两种侵袭性肿瘤,即儿科低分化甲状腺癌和甲状腺胚细胞瘤,也存在 DICER1 突变。这篇综述将讨论 DICER1 肿瘤发生的机制,并描述与种系和体细胞 DICER1 突变相关的甲状腺肿瘤。