Thyroid Gland Hemiagenesis with Multinodular Graves Disease: A Case Report [Multinoduler Graves Hastaliginin Eslik Ettigi Tiroid Hemiagenezili Olgu]
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چکیده
منابع مشابه
Thyroid Gland Hemiagenesis with Multinodular Graves' Disease: A Case Report [Multinodüler Graves' Hastaliğinin Eşlik Ettiği Tiroid Hemiagenezili Olgu]
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' ...
متن کاملThyroid hemiagenesis with Graves' disease, Graves' ophthalmopathy and multinodular goiter.
Thyroid hemiagenesis is a rare congenital anomaly in which one of the thyroid lobes with or without isthmus fails to develop. Here we present a woman patient with thyroid hemiagenesis, Graves' disease and ophthalmopathy with nodular goiter. Fine needle aspiration biopsy of the dominant nodule was suspicious of malignancy. The patient was referred for surgery for total thyroidectomy. Histopathol...
متن کاملThyroid hemiagenesis, Graves' disease and differentiated thyroid cancer: a very rare association: case report and review of literature.
OBJECTIVE Thyroid hemiagenesis is a rare congenital disorder characterized by the absence of a lobe and/or of isthmus. Studies on the association between thyroid hemiagenesis, Graves' disease and differentiated thyroid cancer are rare. CASE PRESENTATION We describe the medical and surgical history of a patient in whom a molecular evaluation was performed. A 36-year-old man presented with symp...
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The classical triad of McCune-Albright syndrome (MAS) consists of polyostotic fibrous dysplasia (FD), skin hyperpigmentation (café-au-lait spots), and endocrine dysfunction, frequently seen in females as precocious puberty. Etiology is genetically based and is explained by mosaicism of activating somatic mutations of the alpha-subunit of Gs protein. Clinical presentation is varied and is depend...
متن کاملHypercalcemia due to Graves' disease in a patient with thyroid hemiagenesis.
Thyroid hemiagenesis is a rare anomaly due to failure of development of one thyroid lobe during embryological life. A lot of thyroid disorders may accompany thyroid hemiagenesis. In this report, we present a case of thyroid hemiagenesis, who had moderate hypercalcemia due to Graves' disease. A 43-year-old woman presented with weight loss of more than 5 kg within one month, heat intolerance, and...
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ژورنال
عنوان ژورنال: Medicine Science | International Medical Journal
سال: 2015
ISSN: 2147-0634
DOI: 10.5455/medscience.2015.04.8249