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Case Report

Thyroid Gland Hemiagenesis with Multinodular Graves' Disease: A Case Report [Multinodüler Graves' Hastaliğinin Eşlik Ettiği Tiroid Hemiagenezili Olgu]

Ayse Arduc, Mazhar Muslum Tuna, Bercem Aycicek Dogan, Gulhan Akbaba, Dilek Berker, Serdar Guler

   

Abstract
Thyroid hemiagenesis (THA) is a rare congenital anomaly. It occurs more frequently in the left lobe and predominantly in women. Most of the cases are asymptomatic. The most frequent associated thyroid disorders with THA are nontoxic nodular goiter and Hashimoto’s thyroiditis whereas association of Graves’ disease with THA is very rare. We present a man patient with THA and multinodular Graves’ disease. A 47-year-old male was admitted with palpitation, hand tremor, and weight loss, and was found to have overt thyrotoxicosis and high TSH receptor antibody (TRAB) levels in laboratory analysis (TSH=0.04 µIU/ml sT4=1.3 ng/dl sT3=4.5 pg/ml TRAB=35 IU/l ). Thyroid ultrasonography revealed multiple thyroid nodules (largest one 6x11x17 mm in diameter) in the right lobe; the left lobe was not visualized. Tc-99m thyroid scan showed increased uptake of radioisotope in the right lobe, and there was no uptake in the left lobe. Based on these findings, the patient was diagnosed with THA and multinodular Graves’ disease, and started on metimazole treatment. Although very rare, Graves’ disease may occur in patients with THA, and it should be considered in the differential diagnosis of patients presenting with hyperthyroidism.

Key words: Thyroid hemiagenesis , Graves’ disease, multinodular goiter

Med-Science. 2015; 4(3): 2575-83

 
Medicine Science Vol:4 Issue:3 Year:2015 PP:2356-2699
Posted in Vol: 4 Issue: 3 Year: 2015 September pp: 2356-2699

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