نتایج جستجو برای: contralateral thyroid hemiagenesis
تعداد نتایج: 102606 فیلتر نتایج به سال:
OBJECTIVES To describe the findings of thyroid ultrasonography (T-US), its contribution to diagnose congenital hypothyroidism (CH) and the best time to perform it. SUBJECTS AND METHODS Forty-four patients with CH were invited to undergo T-US and 41 accepted. Age ranged from 2 months to 45 years; 23 patients were females. All were treated with L-thyroxine; 16 had previously undergone scintigra...
Thyroid hemiagenesis (TH) is characterized by the congenital absence of one thyroid lobe. The aim of this study was to evaluate the calcium-phosphate balance in TH. Twenty patients with TH and 20 controls with a bilobed thyroid were studied. Serum concentrations of total calcium, parathormon and calcitonin were measured. Additionally, the immunohistochemical expression of calcitonin, chromogran...
Teratoma is one of the commonest ovarian tumors. Struma ovarii is a rare cystic teratoma which is predominantly composed of thyroid tissue. Sometimes, this tumor is accompanied by ascites and hydrothorax which suggests Meigs' syndrome. In this paper, a case of struma ovarii and serous cystadenoma in one oval}' and agenesis of contralateral ovary with hypoplasia of Fallopian tube and pseudo-Meig...
INTRODUCTION It is not uncommon for patients with indeterminate thyroid nodules to undergo diagnostic hemithyroidectomy. When the final pathology determines that the nodule is in fact malignant, patients require counseling as to the whether a completion thyroidectomy is necessary. OBJECTIVES 1. Determine the incidence of well differentiated thyroid cancer (WDTC) in the contralateral thyroid l...
Thyroid dysgenesis is the major cause of congenital hypothyroidism in humans. The underlying molecular mechanism is in most cases unknown, but the frequent co-incidence of cardiac anomalies suggests that the thyroid morphogenetic process may depend on proper cardiovascular development. The T-box transcription factor TBX1, which is the most probable gene for the 22q11 deletion syndrome (22q11DS/...
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