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遗传性和散发性甲状腺及甲状旁腺疾病中的分子改变

Molecular alterations in hereditary and sporadic thyroid and parathyroid diseases.

作者信息

Hunt Jennifer L

机构信息

Department of Anatomic Pathology, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.

出版信息

Adv Anat Pathol. 2009 Jan;16(1):23-32. doi: 10.1097/PAP.0b013e3181915f7d.

Abstract

Thyroid and parathyroid diseases are fairly common and can be either hereditary or sporadic in nature. Tumors and tumor-like processes account for the majority of surgical pathology specimens in both of these endocrine organs. Molecular alterations are well known to occur in both the hereditary and the sporadic settings, and include alterations in tumor suppressor genes and oncogenes. The genetic pathways of tumors of parathyroid and thyroid are beginning to be well understood and are proving to be useful diagnostic, prognostic, and potential therapeutic targets. The molecular alterations in parathyroid and thyroid tumors and tumor-like processes are reviewed, with a focus on the potentially clinically useful diagnostic markers.

摘要

甲状腺和甲状旁腺疾病相当常见,其本质上既可以是遗传性的,也可以是散发性的。肿瘤和肿瘤样病变占这两个内分泌器官手术病理标本的大多数。众所周知,遗传性和散发性情况下都会发生分子改变,包括肿瘤抑制基因和癌基因的改变。甲状旁腺和甲状腺肿瘤的遗传途径正开始被深入了解,并被证明是有用的诊断、预后和潜在治疗靶点。本文综述了甲状旁腺和甲状腺肿瘤及肿瘤样病变中的分子改变,重点关注可能具有临床应用价值的诊断标志物。

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