Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep856 | Pituitary and Neuroendocrinology | ECE2023

Carcinoid Syndrome With Mesenteric Ischemia

Alkan Ozlem , Koksalan Damla , Selek Alev , Canturk Zeynep , Cetinarslan Berrin

Introduction: Carcinoid tumors are included in the neuroendocrine tumor family. They are usually seen in the gastrointestinal tract and are asymptomatic unless liver metastases are present.Case Report: A 44-year-old male patient was admitted with chronic crampy abdominal pain, diarrhea, and redness of the face and neck. He was admitted to the emergency department for abdominal pain many times before and was hospitalized in the general surgery department ...

ea0056p695 | Clinical case reports - Pituitary/Adrenal | ECE2018

An acromegaly case; presented from pituitary apoplexia to overt acromegaly before diagnosis

Gonul Burcin , Selek Alev , Cetinarslan Berrin , Canturk Zeynep , Tarkun Ilhan

Pituitary adenomas are the most common lesions of sellar cavity. The usual symptoms are associated with endocrine dysfunctions and mass effects. In this case, a 39 year old female presented with headache for one year and progressive blurred vision, nausea, vomiting for two days. Brain magnetic resonance imaging showed a 16×9 mm hemorrhagic macroadenoma in sellar cavity concordant with apoplexia and anterior pituitary hormone deficiency. The patient underwent transshphenoi...

ea0090p669 | Endocrine-related Cancer | ECE2023

Clinical findings, treatment modality and outcomes of adrenocortical carcinoma: a retrospective review of single tertiary center experience

Selek Alev , Koksalan Damla , Sozen Mehmet , Gezer Emre , Alkan Ozlem , Canturk Zeynep , Cetinarslan Berrin

Background & Aim: Adrenocortical carcinoma (ACC) is an extremely rare malignancy usually with poor outcomes, although the prognosis varies greatly depending on the initial tumor stage. Here we present clinical and outcome diversity of the patients in a single center.Methods: We retrospectively analyzed 16 patients with ACC diagnosed between 2000 and 2022. Demographical findings, hormonal status, radiological findings, ENSAT stage, weiss score and Ki6...

ea0041ep105 | Bone & Osteoporosis | ECE2016

A rare differential diagnosis of Paget’s disease

Cetinarslan Berrin , Selek Alev , Canturk Zeynep , Tarkun Ilhan , Akyay Ozlem Zeynep , Akkas Nagihan

Hypertrophic osteoarthropathy (HOA) is a syndrome characterized with proliferation of bones at the distal parts of extremities. Clubbing, periostitis of tubular bones and non-inflammatory arthritis of lower extremities are commonly seen as a part of this syndrome.66 years old male patient was admitted to our hospital with painful swelling of his left lower extremity for 2 months. He denies any other systemic symptoms such as fever and weight loss. He had...

ea0041ep1030 | Thyroid (non-cancer) | ECE2016

Acute suppurative thyroiditis caused by burkholderia cepacia

Tarkun Ilhan , Akyay Ozlem Zeynep , Canturk Zeynep , Cetinarslan Berrin , Selek Alev , Catan Fatma Tugba

Introduction: The thyroid is generally resistant to infections due to its encapsulated location, high iodine concentration, hydrogen peroxide production, and high levels of blood and lymphoid circulation therefore acute suppurative thyroiditis is rarely seen. The most common agents are Staphilococcus and Streptococcus. In this case we present acute suppurative thyroiditis caused by Burkholdeira cepacia, that is a rare infectious agent in adults.Case: 34 ...

ea0041ep1101 | Thyroid cancer | ECE2016

Papillary thyroid carcinoma in a thyroglossal duct Cyst (TDC) without a thyroid primary

Canturk Zeynep , Catan Fatma Tugba , Cetinarslan Berrin , Tarkun Ilhan , Selek Alev , Akyay Ozlem Zeynep

Introduction: Thyroglossal duct cyst (TDC) is a developmental abnormality of the thyroid gland. Malignancy arising from this duct is very rare. Due to embryological remnants of thyroid tissue located in the TDC, all malignant tumors which develop in the thyroid gland may also develop in the TDC. In case of malignancy, the most probable diagnosis is papillary thyroid carcinoma.Case report: We present a 27-year-old female patient complaining of a midline n...

ea0037ep7 | Adrenal cortex | ECE2015

New onset sarcoidosis after remission of Cushing's syndrome

Canturk Zeynep , Selek Alev , Baris Serap , Cetinarslan Berrin , Tarkun Ilhan , Akyay Zeynep

Introduction: Glucocorticoids, even endogenous or exogenous, suppress the inflammatory response therefore they are the most preferred treatment options in inflammatory diseases. Persistent hypercortisolism induces lymphopenia and lymphoid tissue atrophy. Excessive endogenous hypercortisolism might mask the active inflammatory disease. Rebound immune modulation may occur after Cushing’s syndrome (CS) remission, leading to the new onset of autoimmune diseases.<p class="...

ea0037ep722 | Pituitary: clinical | ECE2015

A rare adventure of a lymphocytic hypophysitis

Canturk Zeynep , Selek Alev , Cetinarslan Berrin , Tarkun Ilhan , Akyay Zeynep , Cabuk Burak , Ceylan Savas

Introduction: Lymphocytic hypophysitis is a rare endocrine disease involving lymphocytic infiltration and chronic pituitary inflammation. It may result in significant morbidity by loss of pituitary functions and neurological deficits. Pituitary abscess is another rare disease which may be associated with underlying parasellar pathology. Here, we report a case of lymphocytic hypophysitis diagnosed with a pituitary abscess and recurrent suprasellar involvement after surgery....

ea0037ep760 | Pituitary: clinical | ECE2015

Assessment of mean platelet volume in acromegaly and its relation with disease outcome

Cetinarslan Berrin , Akyay Ozlem Zeynep , Selek Alev , Batman Adnan , Canturk Zeynep , Tarkun Ilhan

Background: Acromegaly is associated with increased risk of coronary atherosclerosis and cardiovascular mortality. Changes in coagulation and fibrinolysis markers in acromegalic patients have been shown to indicate increase in the risk of developing cardiovascular disease. Mean platelet volume (MPV) is a marker of platelet functions and activity, and increased MPV is an independent risk factor of myocardial infarction and thrombotic events. In this study, we examined the level...

ea0037ep761 | Pituitary: clinical | ECE2015

A rare case of papillary thyroid cancer: pituitary metastasis

Akyay Ozlem Zeynep , Cetinarslan Berrin , Tarkun Ilhan , Canturk Zeynep , Selek Alev , Batman Adnan

Introduction: Differentiated thyroid carcinoma (DTC) rarely represents with distant organ metastasis. Cerebral metastasis is seen in 0.4–1.2% of patients with distant organ metastasis. There are only 14 patients of DTC with pituitary metastasis reported in the literature. Here, we report a papillary thyroid carcinoma (PTC) patient represented with pituitary metastasis.Case: A 68-year-old male patient has admitted to our hospital with a growing tumou...