Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep846 | Clinical case reports - Pituitary/Adrenal | ECE2017

Breast cancer and newly discovered non-secretor pituitary mass- as risk of metastases?

Valea Ana , Oprisor Iulia , Carsote Mara , Pop Dan Dumitru , Morar Andra , Ghervan Cristina , Georgescu Carmen Emanuela

Introduction: Even if breast cancer is rare cause of pituitary metastases, the diagnosis of a pituitary adenoma, shortly after surgery for breast cancer, raises suspicion of a possible secondary determinations.Material and method: This is a case report revealing the medical history and endocrine profile of a female with breast cancer and pituitary macroadenoma.Case data: A 64-year old non-smoking female (with menopause at age of 52...

ea0041ep49 | Adrenal cortex (to include Cushing's) | ECE2016

Cushing’ s disease, hasimoto’s thyroiditis and severe hyperandrogenemia

Valea Ana , Ciocan Irina , Carsote Mara , Morar Andra , Pop Dan Dumitru , Ghervan Cristina , Georgescu Carmen Emanuela

Introduction: Cushing’s disease (CD) is caused by high adrenocorticotropic hormone (ACTH), usually by a pituitary microadenoma.Material and method: This is a case report investigated in several Romanian centers by performing: morning plasma cortisol, circadian rhythm of plasma cortisol, plasma ACTH, dexamethasone (DXM) suppression tests.Case data: A 57-year female, known with hypertension and osteopenia, was ...

ea0041ep51 | Adrenal cortex (to include Cushing's) | ECE2016

Pediatric Cushing’s disease and paraduodenal tumor

Valea Ana , Breaban Maria , Carsote Mara , Morar Andra , Dumitru Pop Dan , Emanuela Georgescu Carmen , Ghervan Cristina

Introduction: Cushing’s disease (CD) in youth represents a challenge especially related to the therapy and long-term management.Materials and methods: We report the medical history of a child with CD who was followed-up for 7 years. Suggestive endocrine panel and imagery is exposed.Case presentation: A 19-year female was diagnosed at age of 12 with CD. Clinical assessment revealed: weight gain, headache, hyperpigmentation pred...

ea0041ep167 | Calcium and Vitamin D metabolism | ECE2016

Adult iatrogenic hypoparathyroidism therapy: between less and more

Terec Adina , Morar Andra , Carsote Mara , Pop Dan Dumitru , Georgescu Carmen Emanuela , Valea Ana

Introduction: The hypoparathyroidism (HypoPT) represents a rare condition characterized by low calcium (Ca) and parathyroid hormone (PTH) levels, frequently due to thyroid surgery by direct trauma of the parathyroid glands, devascularization, or their accidental removal. Postoperative hypoparathyroidism-related hypocalcemia may be permanent or transient.Case report: We report the case of a 64-year-old man presenting with severe symptoms of hypocalcemia (...

ea0041ep936 | Pituitary - Clinical | ECE2016

Mesocorticotropinoma- associated Nelson’s syndrome: 28 years of follow-up

Marcusan Alexandra , Morar Andra , Carsote Mara , Dumitru Pop Dan , Ghervan Cristina , Emanuela Georgescu Carmen , Valea Ana

Introduction: Nelson’s syndrome (NS) is an exceptionally rare condition diagnosed sometimes after bilateral suprarenalectomy for Cushing’s disease (CS) involving rapid enlargement of a pre-existing ACTH-secreting pituitary tumor. The clinical picture varies from hyperpigmentation, headache and visual disturbance to diabetes insipidus and hypopituitarism if the hypothalamic-pituitary portal system is disrupted or normal pituitary tissue is destroyed by the adenoma. Th...

ea0037ep1283 | Clinical Cases–Thyroid/Other | ECE2015

Petrified ears associated with Schmidt's syndrome

Valea Ana , Morar Andra , Breaban Maria , Tomesc Florica , Terec Adina , Iacob Iulia , Pop Dan Dumitru , Silaghi Alina , Ghervan Cristina

Introduction: Bilateral calcification of auricular cartilage is an uncommonly reported condition. The aetiology of this phenomenon is still unclear. Petrified ears have seldom been described in association with endocrinopathies such as adrenal insufficiency, hypothyroidism, diabetes mellitus, and acromegaly.Case report: We present the case of a 42 year-old male patient, diagnosed with Addison’s disease at the age of 14, currently undergoing treatmen...