Endocrine Abstracts

Cushing’s syndrome is rare in males. Hypercortisolic consequences on male gonadal function are unknown. The aim of our study is to research gonadal and sexual abnormalities in 17 male subjects with endogenous cortisol excess: 10 Cushing’s diseases, 5 paraneoplastic Cushing syndrome, 1 malignant corticosurrenaloma, 1 micronodular dysplasia. Their mean age is 30.2 years (18 – 50). Our work is based on anamnestic, clinical and hormonal results. Our population is co...

Cushing’s syndrome is rare in males. Hypercortisolic consequences on male gonadal function are unknown. The aim of our study is to research gonadal and sexual abnormalities in 17 male subjects with endogenous cortisol excess: 10 Cushing’s diseases, 5 paraneoplastic Cushing syndrome, 1 malignant corticosurrenaloma, 1 micronodular dysplasia. Their mean age=30.2 years (18–50). Our work is based an anamnestic, clinical and hormonal results. Our population is compare...

Aim: Brown tumors are a very rare and serious complication of sustained undiagnosed secondary hyperparathyroidism. Diagnosis and differential diagnosis are made by combining clinical, biochemical, radiological and pathological findings. We present the case of a male with chronic renal disease and multiple bone damage.A 58-year-old male was referred to the endocrine clinic because of lower back and pleural pain. He was an obese smoker with a heavy medical...

Introduction: Medullary thyroid carcinoma (MTC) originated from parafollicular C cells of the thyroid gland is a rare histological type of malignancy. Common sites of metastases are liver, lungs and bones, while metastases in other sites are extremely rare. Breast metastases from MTC are reported in 20 cases, and only in women.Case report: A 67-year-old man was presented after thyroidectomy for further evaluation and treatment. Histology was positive for...

Introduction: Tyrosine kinase inhibitors (sorafenib and sunitinib) have been used in treating refractory cases of thyroid cancer. The aim of our present study was to assess the efficacy of these agents in patients with refractory and progressive thyroid cancer, regarding patients’ quality of life, adverse events and response ratesPatients and methods: We retrospectively analyzed data of adult patients with differentiated and medullary thyroid cancer...

Thyroid cancer in patients with hyperthyroidism is considered to be a rare event and its course seems to be more aggressive in patients with Graves’ disease. The coexistence of medullary thyroid cancer and hyperthyroidism is very rare and there are only 14 cases reported in the literature.The aim of this retrospective study is to assess the clinical and histological characteristics and the evolution of thyroid cancer in patients with different types...

Aim: The aim of this retrospective study was to evaluate the diagnostic significance of presurgical thyroid ultrasound in comparison with FNAC of thyroid nodules and their contribution in detecting thyroid cancer.Patients and methods: We retrospectively studied the files of 118 thyroid cancer patients, 18 men (15.2%) and 100 women (84.8%), who underwent thyroidectomy from January 2013 until December 2016, in the Department of Surgical Oncology of Theagen...

Introduction: Women with non-metastatic breast cancer form a distinct subpopulation in which calcium homeostasis in response to treatment with denosumab has not been extensively investigated.Methods: Female patients with osteoporosis, who were eligible for treatment with denosumab, were prospectively enrolled (2011–2012) and divided into two groups; Group A consisting of patients with either no history or benign diseases non affecting bone metabolis...

Introduction Thyroid cancer (TC) is rare in childhood. The aim of the present study was to describe the tumoral characteristics of children and adolescents with TC and to investigate the frequency of microcarcinomas in that population.Methods We studied the medical records of 101 children and adolescents (≤ 21 years-old) who were diagnosed with TC between January 1977 and December 2011 in Theagenio Cancer Hospital. The following characteristics wer...

BackgroundCystic parathyroid adenoma is a rare entity (<0.01% of all cervical masses) that leads to primary hyperparathyroidism in 9% of cases. Parathyroid scintigraphy is essential for the diagnosis although there are pitfalls with false negative results. Parathyroidectomy is the treatment of choice but its success depends on the exact preoperative localization of the parathyroid lesions. 4D-CT is a very helpful diagnostic tool in such cases.<p ...