先天性甲状腺偏侧缺如合并Graves病及单侧甲状腺结节：附1例报告并文献复习

doi:10.3969/j.issn.2095-378X.2024.01.011

Abstract

Abstract: Objective To investigate the clinical characteristics, pathogenesis, diagnosis, and treatment of patients with congenital thyroid hemiagenesis （TH） complicated with Graves’ disease and thyroid nodule. Methods A retrospective analysis was conducted on a patient with right TH associated with Graves’ disease and left thyroid nodule, and relevant literature was reviewed. Results A patient presented to the clinic with hyperthyroidism. Thyroid function examination and thyroid ¹³¹I uptake test suggested Graves’ disease. Thyroid ultrasound scan demonstrated absence of the right lobe with left thyroid nodule （TI-RADs Ⅳb）. Methimazole was used to control hyperthyroidism and thyroid nodule were followed. Conclusion The combination of TH, Graves’ disease, and thyroid nodule is extremely rare. A better comprehension of such patients through case report and literature review is essential for clinical intervention.

Key words: Thyroid hemiagenesis, Graves' disease, Thyroid nodule

CLC Number:

R736.1

SUN Jinyu, MA Qiang. Graves’ disease and unilateral thyroid nodule in congenital thyroid hemiagenesis： One case report and literature review[J]. Surgical Research and New Technique, 2024, 13(1): 48-50.

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Graves’ disease and unilateral thyroid nodule in congenital thyroid hemiagenesis： One case report and literature review

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