成熟卵巢畸胎瘤并发STRN::ALK融合的甲状腺乳头状癌。

IF 1.7 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Ambrus Mályi, Erika Tóth, Ildikó Vereczkey, Andrea Kohánka, Zsombor Melegh
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引用次数: 0

摘要

由成熟卵巢畸胎瘤引起的躯体恶性肿瘤是一种罕见的现象,发生率为1%至3.5%。这些躯体肿瘤最常见的是表皮恶性肿瘤,但它们可以从任何躯体部分发展,包括甲状腺组织。越来越多的证据表明,在这种情况下,发病机制是由相同的突变谱驱动的,就像在他们的传统体细胞对偶中看到的那样。在这里,我们报告第一例STRN::ALK融合在乳头状甲状腺癌引起的甲状腺成分成熟卵巢畸胎瘤。患者右侧卵巢出现68毫米肿块,经组织病理学证实为成熟畸胎瘤。在甲状腺部分,发现甲状腺乳头状癌。新一代测序显示STRN::ALK融合,癌组织中ALK免疫组化阳性。这些遗传特征的识别不仅有助于诊断,而且在疾病进展的情况下提供潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Papillary Thyroid Carcinoma With an STRN::ALK Fusion Arising From a Mature Ovarian Teratoma.

Somatic malignancy arising from a mature ovarian teratoma is a rare phenomenon, occurring in 1% to 3.5% of cases. These somatic tumors are most commonly epidermal malignancies, but they can develop from any somatic component, including thyroid tissue. Increasing evidence suggests that in such cases, the pathogenesis is driven by the same mutational profile as seen in their conventional somatic counterparts. Here, we report the first case of an STRN::ALK fusion in a papillary thyroid carcinoma arising from the thyroid component of a mature ovarian teratoma. The patient presented with a 68 mm mass in the right ovary, which was histopathologically confirmed as a mature teratoma. Within the thyroid component, papillary thyroid carcinoma was identified. Next-generation sequencing revealed an STRN::ALK fusion, supported by positive ALK immunohistochemistry in the carcinoma. The identification of these genetic signatures not only aids in diagnosis but also provides potential therapeutic targets in the case of disease progression.

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来源期刊
CiteScore
3.90
自引率
12.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.
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