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罕见的甲状腺非肿瘤性疾病。

Rare thyroid non-neoplastic diseases.

作者信息

Lacka Katarzyna, Maciejewski Adam

机构信息

Department of Endocrinology, Metabolism and Internal Medicine, University of Medical Sciences, Poznan, Poland.

出版信息

Thyroid Res. 2015 Apr 11;8:5. doi: 10.1186/s13044-015-0017-3. eCollection 2015.

Abstract

Rare diseases are usually defined as entities affecting less than 1 person per 2,000. About 7,000 different rare entities are distinguished and, among them, rare diseases of the thyroid gland. Although not frequent, they can be found in the everyday practice of endocrinologists and should be considered in differential diagnosis. Rare non-neoplastic thyroid diseases will be discussed. Congenital hypothyroidism's frequency is relatively high and its early treatment is of vital importance for neonatal psychomotor development; CH is caused primarily by thyroid dysgenesis (85%) or dyshormonogenesis (10-15%), although secondary defects - hypothalamic and pituitary - can also be found; up to 40% of cases diagnosed on neonatal screening are transient. Inherited abnormalities of thyroid hormone binding proteins (TBG, TBP and albumin) include alterations in their concentration or affinity for iodothyronines, this leads to laboratory test abnormalities, although usually with normal free hormones and clinical euthyroidism. Thyroid hormone resistance is most commonly found in THRB gene mutations and more rarely in THRA mutations; in some cases both genes are unchanged (non-TR RTH). Recently the term 'reduced sensitivity to thyroid hormones' was introduced, which encompass not only iodothyronine receptor defects but also their defective transmembrane transport or metabolism. Rare causes of hyperthyroidism are: activating mutations in TSHR or GNAS genes, pituitary adenomas, differentiated thyroid cancer or gestational trophoblastic disease; congenital hyperthyroidism cases are also seen, although less frequently than CH. Like other organs and tissues, the thyroid can be affected by different inflammatory and infectious processes, including tuberculosis and sarcoidosis. In most of the rare thyroid diseases genetic factors play a key role, many of them can be classified as monogenic disorders. Although there are still some limitations, progress has been made in our understanding of rare thyroid diseases etiopathogenesis, and, thanks to these studies, also in our understanding of how normal thyroid gland functions.

摘要

罕见病通常定义为每2000人中患病人数少于1人的疾病。已识别出约7000种不同的罕见病,其中包括甲状腺罕见病。虽然并不常见,但内分泌科医生在日常诊疗中会遇到这些疾病,在鉴别诊断时应予以考虑。本文将讨论罕见的非肿瘤性甲状腺疾病。先天性甲状腺功能减退症的发病率相对较高,其早期治疗对新生儿的精神运动发育至关重要;先天性甲状腺功能减退症主要由甲状腺发育不全(85%)或甲状腺激素合成障碍(10 - 15%)引起,不过也可发现继发性缺陷——下丘脑和垂体方面的缺陷;新生儿筛查确诊的病例中,高达40%为暂时性的。甲状腺激素结合蛋白(甲状腺球蛋白、甲状腺素结合前白蛋白和白蛋白)的遗传性异常包括其浓度改变或对碘甲状腺原氨酸的亲和力改变,这会导致实验室检查异常,不过通常游离激素正常且临床甲状腺功能正常。甲状腺激素抵抗最常见于甲状腺激素受体β基因突变,较少见于甲状腺激素受体α基因突变;在某些情况下,两个基因均无变化(非TR RTH)。最近引入了“对甲状腺激素敏感性降低”这一术语,它不仅包括碘甲状腺原氨酸受体缺陷,还包括其跨膜转运或代谢缺陷。甲状腺功能亢进症的罕见病因有:促甲状腺激素受体或GNAS基因的激活突变、垂体腺瘤、分化型甲状腺癌或妊娠滋养细胞疾病;也可见先天性甲状腺功能亢进症病例,不过比先天性甲状腺功能减退症少见。与其他器官和组织一样,甲状腺可受到不同炎症和感染性疾病的影响,包括结核病和结节病。在大多数罕见甲状腺疾病中,遗传因素起关键作用,其中许多可归类为单基因疾病。尽管仍存在一些局限性,但我们对罕见甲状腺疾病发病机制的理解已取得进展,并且由于这些研究,我们对正常甲状腺功能的理解也有所进步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d591/4407423/69446b77c434/13044_2015_17_Fig1_HTML.jpg

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