Searchable abstracts of presentations at key conferences in endocrinology

ea0032p287 | Clinical case reports - Thyroid / Others | ECE2013

Postmenopausal hirsutism and hyperandrogenemia due to granulosa cell tumor of the ovary

Bahadir Cigdem , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Inroduction: Progressive baldness and severe hirsutism associated with granulosa cell tumor of ovaries are rare conditions in women. Reported cases are usually pubertal girls and young women. Here, we report a case of postmenopausal baldness and hirsutism due to granulosa cell tumor of the ovary.Case report: A 62 year-old woman presented with baldness and hirsutism on her face, body and back for 3 years. She had menarche at 14 years and menopause at 52 y...

ea0032p109 | Bone and Osteoporosis | ECE2013

A patient osteogenesis imperfecta with osteoporosis

Ecemis Gulcin Cengiz , Kan Elif Kilic , Bahadir Cigdem Tura , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Introduction: Osteogenesis imperfecta (OI) is a congenital, generalized connective tissue disorder characterized by severe osteoporosis and bone fragility. OI is most commonly caused by mutations in genes encoding the α-1 and α-2 chains of type I collagen or proteins involved in posttranslational modification of type I collagen. Although, no controlled studies are done, bisphosphonates are used for the treatment of OI. I.v. bisphosphonates are reported to be more eff...

ea0032p264 | Clinical case reports – Pituitary/Adrenal | ECE2013

Cases with adrenocortical carcinoma

Ecemis Gulcin Cengiz , Kan Elif Kilic , Bahadir Cigdem Tura , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Introduction: Adrenocortical carcinoma (ACC) is a rare cancer (estimated incidence, 0.7 to 2.0 cases per 1 million population per year) with a poor prognosis. Even after seemingly complete surgical resection, most patients develop recurrence within 5 years. The 5-year survival rate is <15% among patients with metastatic disease.Methods: We present the results of six patients with adrenocortical carcinoma followed in our clinic....

ea0032p952 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

An acromegalic patient with giant tumor

Ecemis Gulcin Cengiz , Kan Elif Kilic , Bahadir Cigdem Tura , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Introduction: Acromegaly is a disease caused by excessive secretion of GH. The cause of acromegaly is GH secreting pituitary adenoam in 99% of the cases. It is estimated that 5% of pituitary adenomas become invasive and may grow to gigantic sizes (>4 cm in diameter). Here, we present a 31 years old acromegalic woman with a delayed diagnosis of a giant invasive pituiatary adenoma.Case report: A 31-year-old woman admitted to our hospital for oligomenor...

ea0037ep19 | Adrenal cortex | ECE2015

Association of psoriasis with Cushing's syndrome

Bahadir Cigdem Tura , Gokosmanoglu Feyzi , Kan Elif Kilic , Ecemis Gulcin Cengiz , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Introduction: Psoriasis is a chronic, inflammatory and T-cell mediated autoimmune disease of skin. Its prevalence is 2–3%. It may improve due to immunesupressive effects of hypercortisolaemia during the active phase of Cushing’s syndrome (CS) and may exacerbate after treatment. The aim of this study was to investigate association of psoriasis with CS.Methods: We prospectively followed 62 patients who had been diagnosed with CS between 2010 and ...

ea0037ep20 | Adrenal cortex | ECE2015

Should Cushing syndrome be only evaluated by endocrinologists and neurosurgeons?

Bahadir Cigdem Tura , Gokosmanoglu Feyzi , Kan Elif Kilic , Ecemis Gulcin Cengiz , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Objective: Physical features such as central obesity, purple stria, thin skin, moon face and buffalo hump may be observed in Cushing’s syndrome (CS). Psychiatric and psychological disturbances may also be present in addition to the physical problems. The most common mental disturbance is major depression. Mania and anxiety disorders may also be seen. It may be detected both in active period or in remission of CS on account of persistent effect of previous period of hyperc...

ea0037ep21 | Adrenal cortex | ECE2015

Necessity of thrombophylaxis in Cushing's syndrome

Bahadir Cigdem Tura , Gokosmanoglu Feyzi , Kan Elif Kilic , Ecemis Gulcin Cengiz , Atmaca Aysegul , Atmaca Hulusi , Colak Ramis

Introduction: Cushing’s syndrome (CS) is accompanied by a ten times increased risk of venous thromboembolism and arterial thrombosis. In this study we aimed to analyze frequency of thromboembolism in CS.Methods: We prospectively followed 62 patients who had been diagnosed with CS between 2010 and 2014 in our clinic. Of the patients, 60% had Cushing’s disease (CD) (29 females and eight males) and 40% had ACTH-independent CS (20 females and five ...

ea0016p13 | Adrenal | ECE2008

The prevalence of non-classic adrenal hyperplasia among Tturkish women with hirsutism

Unluhizarci Kursad , Kula Mustafa , Dundar Munis , Tanriverdi Fatih , Israel Shoshana , Colak Ramis , Dokmetas Hatice S , Atmaca Hulusi , Bahceci Mithat , Balci M Kemal , Comlekci Abdurrahman , Akarsu Ersin , Bilen Habip , Erem Cihangir , Kelestimur Fahrettin

Context: The prevalence of NCAH among Turkish women with hirsutism has not been established so far.Objective: To evaluate the prevalences of 21-hydroxylase (21-OHD) and 11-β hydroxylase deficiencies by ACTH stimulation test among hirsute women.Patients and methods: The study population consisted of 285 premenopousal women, aged 16–46 years (mean: 23.2±0.3). All were hirsute and hyperandrogenic. Androgen secreting tum...