Microscopic characteristics of adult dyshormonogenetic goiter: attempt to histologically estimate subtypes.

IF 2.5 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Mitsuyoshi Hirokawa, Hanna Deguchi-Horiuchi, Shuji Fukata, Miyoko Higuchi, Ayana Suzuki, Eijun Nishihara, Takahiko Kogai, Akira Hishinuma, Akira Miyauchi, Takashi Akamizu
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Abstract

In adults, cases of dyshormonogenetic goiter (DG) that go undiagnosed during childhood may necessitate thyroidectomy due to unexplained thyroid enlargement, often presenting diagnostic challenges. This study aimed to characterize the histopathological features of the thyroid in adult DG cases, and to evaluate the feasibility of predicting subtypes from the findings. Fifty adult patients with DG confirmed by the presence of gene variants were included. All resected thyroids showed diffuse goiter with microscopically altered thyroid follicles throughout the gland. All patients with SLC5A5 abnormality (iodide transport defect) showed lobulation accentuated by interlobular fibrosis. Follicular cells were enlarged, except in patients with SLC26A4 abnormality (Pendred syndrome). A scant colloid was observed in all patients with thyroglobulin (TG) gene abnormality. Thyroid peroxidase (TPO) gene abnormality and SLC26A4 abnormality were characterized by large follicles with Sanderson's polsters. Multiple non-encapsulated nodular lesions were present except in two patients with SLC26A4 abnormality. These were mainly follicular thyroid adenoma-like nodules associated with TG gene abnormality, TPO gene abnormality, and SLC5A5 variant. With SLC26A4 abnormality, the nodules were follicular nodular disease-like. The proposed histological framework may be particularly valuable for adult patients undergoing thyroidectomy for unexplained diffuse enlargement or multinodularity, particularly when no prior diagnosis of DG is documented.

成人甲状腺肿的显微特征:试图从组织学上估计亚型。
在成人中,由于不明原因的甲状腺肿大,儿童时期未确诊的激素单性甲状腺肿(DG)可能需要甲状腺切除术,这通常带来诊断上的挑战。本研究旨在描述成年DG患者甲状腺的组织病理学特征,并评估从结果预测亚型的可行性。纳入了50例经基因变异证实的成年DG患者。所有切除的甲状腺均表现为弥漫性甲状腺肿,镜下可见甲状腺滤泡改变。所有SLC5A5异常(碘离子转运缺陷)的患者均表现为小叶化,小叶间纤维化加重。除SLC26A4异常(Pendred综合征)患者外,滤泡细胞增大。所有甲状腺球蛋白(TG)基因异常患者均可见少量胶质。甲状腺过氧化物酶(TPO)基因异常和SLC26A4基因异常以大卵泡伴Sanderson氏息肉为特征。除2例SLC26A4异常外,均有多发非包封性结节病变。这些主要是滤泡性甲状腺腺瘤样结节,与TG基因异常、TPO基因异常和SLC5A5变异相关。SLC26A4异常,结节呈滤泡性结节样病变。所提出的组织学框架对于因不明原因的弥漫性增大或多结节性甲状腺切除的成年患者尤其有价值,特别是在没有DG诊断记录的情况下。
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来源期刊
Endocrine journal
Endocrine journal 医学-内分泌学与代谢
CiteScore
4.30
自引率
5.00%
发文量
224
审稿时长
1.5 months
期刊介绍: Endocrine Journal is an open access, peer-reviewed online journal with a long history. This journal publishes peer-reviewed research articles in multifaceted fields of basic, translational and clinical endocrinology. Endocrine Journal provides a chance to exchange your ideas, concepts and scientific observations in any area of recent endocrinology. Manuscripts may be submitted as Original Articles, Notes, Rapid Communications or Review Articles. We have a rapid reviewing and editorial decision system and pay a special attention to our quick, truly scientific and frequently-citable publication. Please go through the link for author guideline.
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