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Congenital thyroid hemiagenesis with multinodular goiter

机译:先天性甲状腺造血合并多结节性甲状腺肿

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Thyroid hemiagenesis is a rare form of thyroid dysgenesis characterized by an absence of half of the thyroid gland. Developmental hemi-thyroid anomalies can result from either an abnormal descent or an agenesis of one lobe of the thyroid gland. We report a case of a 40-year-old woman with history of a longstanding gradually progressive thyroid swelling without any complication. An ultrasonographic examination diagnosed the absence of the left thyroid lobe and enlargement of the right lobe, which was confirmed on a computed tomography (CT) angiogram and a radionuclide scan of the neck. A cytological examination showed nodular goiter with cystic degeneration. Right subtotal thyroidectomy was performed and histopathological examination confirmed adenomatous goiter with degenerative changes. We report the rarity of the condition and emphasize the role of a comprehensive radiological, cytological, and radionuclide algorithm for an accurate preoperative diagnosis and subsequent management.
机译:甲状腺造血是甲状腺发育不良的一种罕见形式,其特征是缺乏一半的甲状腺。甲状腺半球异常下降或发育异常可导致发育性半甲状腺异常。我们报道一例40岁女性,有长期逐渐进行性甲状腺肿大而无任何并发症的病史。超声检查诊断为左甲状腺叶不存在,右叶肿大,这是通过计算机断层扫描(CT)血管造影和颈部放射性核素扫描证实的。细胞学检查显示结节性甲状腺肿伴囊性变性。右半全甲状腺切除术,组织病理学检查证实腺瘤性甲状腺肿有退行性改变。我们报告这种情况的稀有性,并强调了全面的放射学,细胞学和放射性核素算法对于准确的术前诊断和后续治疗的作用。

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