Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep1193 | Clinical Cases–Pituitary/Adrenal | ECE2015

Case report: an acromegalic patient presented with dysphagia

Gokosmanoglu Feyzi , Bahadir Cigdem Tura , Kan Elif Kilic , Atmaca Aysegul

Introduction: Acromegaly is a chronic disease characterized by prognatism, frontal bossing, coarsened facial features, enlarged hands and feet due to overproduction of growth hormone (GH) generally by a pituitary adenoma. Here, we aimed to present an acromegalic patient presented with retropharyngeal hypertrophy first time in the literature.Case report: 65-year-old female patient had been referred to our department from otorhinolaryngology outpatient-cli...

ea0037ep1281 | Clinical Cases–Thyroid/Other | ECE2015

Multiple endocrine organ failure due to amyloidosis

Gokosmanoglu Feyzi , Bahadir Cigdem Tura , Kan Elif Kilic , Atmaca Aysegul

Introduction: Amyloidosis is characterised by accumulation of amorph and proteinous substance in several tissues and organs. Thyroid, adrenal, and pituitary insufficiencies may rarely be observed due to accumulation of these substances. Here, we present a case to point out this rare condition.Case report: A 19-year-old male patient admitted with complaints of swelling in the neck, abnormality in thyroid hormone levels and fatigue. He had been diagnosed w...

ea0035p274 | Clinical case reports Thyroid/Others | ECE2014

A rare variant of papillary carcinoma of thyroid: Warthin-like variant

Bahadir Cigdem Tura , Kan Elif Kilic , Gokosmanoglu Feyzi , Atmaca Aysegul , Kefeli Mehmet

Introduction: Warthin-like papillary thyroid carcinoma (WLPTC) is a rare variant of thyroid papillary carsinoma (TPC). We present these cases to point out this rare variant.Case reports: Case 1: A 38-year-old woman admitted to outpatient clinic with a thyroid nodule. Ultrasonography of thyroid gland revealed bilateral multinodular goiter with microcalcifications. Thyroid autoantibodies were elevated. Thyroid function tests (TFT) were normal. Fine-needle ...

ea0035p275 | Clinical case reports Thyroid/Others | ECE2014

Mixed medullary and papillary carcinoma of thyroid

Bahadir Cigdem Tura , Gokosmanoglu Feyzi , Kan Elif Kilic , Atmaca Aysegul , Kefeli Mehmet , Akpinar Sinan

Introduction: Despite having different embriogenic origins, thyroid medullary carcinoma and follicular carcinoma may be seen together as mixed medullary-follicular thyroid carcinoma. We present a rare case of mixed medullary-follicular cell carcinoma of thyroid which has a progressive and aggressive nature.Case report: A 68-year-old female patient admitted with complaint of a lump in her neck. Ultrasonography of thyroid gland revealed a 37×35 mm sol...

ea0035p1110 | Thyroid Cancer | ECE2014

Metastatic thyroid papillary microcarcinomas

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

Aim: Thyroid papillary carcinomas smaller than 1 cm are called papillary microcarcinomas (PMC). They rarely metastasize to lymph node (LN) and distant areas. The presence of palpable lymphadenopathy at the time of diagnosis shows high risk of recurrence regardless of primary tumor size. We aimed to investigate histopathologic characteristics and recurrence frequency of thyroid PMCs with LN metastasis (LNM).Materials and methods: Thyroid PMC cases with LN...

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...