Searchable abstracts of presentations at key conferences in endocrinology

ea0070aep582 | Pituitary and Neuroendocrinology | ECE2020

An asynchronous double growth hormone secreting pituitary adenoma ofa different proliferative potential – a case report

Trofimiuk-Muldner Malgorzata , Domagała Bartosz , Kluczynski Lukasz , Sokolowski Grzegorz , Zielinski Grzegorz , Maksymowicz Maria , Pekul Monika , Hubalewska-Dydejczyk Alicja

Background: Double pituitary adenomas are a rare entity, which requires clinical attention and a careful follow-up.Case report: A 37-year-old man presented with left-sided painful gynecomastia. He denied typical symptoms of excessive growth hormone (GH) secretion and did not show any acromegalic features. Due to low testosterone and LH levels with mild hyperprolactinaemia, the patient was referred to pituitary MR, which revealed an 11 × 13 mm right-...

ea0032p895 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Cushing's disease in children – the effectiveness and complications of transsphenoidal surgery

Witek Przemyslaw , Zielinski Grzegorz

Introduction: Generously supported by IPSEN)-->ACTH-secreting pituitary adenomas are the most common cause of endogenous hypercortisolemia in children after 10 years of age. In spite of this pediatric Cushing’s disease (pCD) is a rare medical condition. Transsphenoidal surgery (TSS) remains the treatment of choice but – according to literature date – results of such a procedure could be worse comparatively to adult pop...

ea0032p924 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

Endoscopic transsphenoidal surgery for acromegaly: assessing the surgical outcome based on current criteria of remission

Zielinski Grzegorz , Witek Przemyslaw , Podgorski Jan

Introduction: Generously supported by IPSEN)-->Acromegaly is associated with increased morbidity and mortality, mainly due to cardiovascular and metabolic complications and higher risk of malignancy. The treatment of choice is selective transsphenoidal surgery (TSS). Successful removal of somatotroph adenoma normalizes GH and IGF1 levels, which improves the patients prognosis. The efficacy of TSS depends on the tumor volume, parasell...

ea0037ep829 | Pituitary: clinical | ECE2015

Glucose homeostasis alterations in Cushing's disease: epidemiology, anthropometric assessment and the role of family history of type 2 diabetes

Witek Przemyslaw , Witek Joanna , Zielinski Grzegorz , Blazik Marlena , Kaminski Grzegorz

Introduction: Cushing’s disease (CD) leads to glucose homeostasis alterations, obesity, unfavorable changes in body composition and cardiovascular complications.Aim of study: i) Prospective evaluation of the frequency of pre-diabetes and diabetes. ii) Assessment of insulin resistance (IR) indices in CD. iii) Analysis of the influence of family history of type 2 diabetes (T2D) on the anthropometry in CD.Methods: The study group...

ea0037ep830 | Pituitary: clinical | ECE2015

Cushing's disease: reversibility of glucose homeostasis alterations and improvement in insulin resistance indices following a successful, transsphenoidal surgery

Witek Joanna , Witek Przemyslaw , Zielinski Grzegorz , Blazik Marlena , Kaminski Grzegorz

Introduction: Cortisol excess in Cushing’s disease (CD) leads to glucose homeostasis alterations and increased cardiovascular risk.Aim of the study: i) To assess the reversibility of glucose homeostasis alterations and dynamics of inflammatory and coagulation parameters after the successful transsphenoidal surgery (TSS) for CD. ii) Analysis of the early improvement in insulin resistance (IR) indices following TSS.Methods: The ...

ea0035p222 | Clinical case reports Pituitary/Adrenal | ECE2014

Hyponatremia as a first symptom of hypopituitarism in an adult patient with natural history of craniopharyngioma undiagnosed since childhood

Witek Przemyslaw , Kaminski Grzegorz , Witek Joanna , Zielinski Grzegorz

Background: Craniopharyngiomas may lead to pituitary insufficiency and neurological symptoms. However the rate of the tumor growth and the time of developing hypopituitarism are difficult to predict.Case report: A 68-year-old male of short stature (height 148 cm) was admitted to the area hospital due to loss of consciousness. The acute coronary syndrome and stroke had been excluded but laboratory tests showed hyponatremia of 106 mmol/l. Hormone measureme...

ea0035p229 | Clinical case reports Pituitary/Adrenal | ECE2014

A case of hypopituitarism caused by lung cancer metastasis to the pituitary

Kaluzny Marcin , Bolanowski Marek , Zielinski Grzegorz , Piesiak Pawel , Maksymowicz Maria

Pituitary tumor is a rare endocrine disorder. In the majority of cases, they are secreting prolactin and/or GH. Pituitary metastatic tumors are localized more often in the nervous than adenomatous hypophysis. Lung, breast and large intestine cancers metastases are found in the pituitary in the most cases. They cause hypopituitarism and local complications. The most often complications found are an optic nerve chiasm pressure or infiltration with a visual field loss, cavernous ...

ea0035p903 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Cushing's disease: the dynamics of serum cortisol concentrations after successful transsphenoidal surgery and the restoration of the adrenal cortex function

Witek Przemyslaw , Zielinski Grzegorz , Witek Joanna , Kaminski Grzegorz

Introduction: Effective surgical treatment of Cushing’s disease (CD) is associated with a rapid decrease in the serum cortisol concentration, which requires the introduction of the hydrocortisone replacement treatment. However, the time of restoration of adrenal function is difficult to predict. The aim of the study was to evaluate the dynamics of serum cortisol concentrations after successful transsphenoidal surgery and to determine the time to restore the function of th...

ea0035p925 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Conservative management of pituitary apoplexy – own experience

Styk Andrzej , Zielinski Grzegorz , Witek Przemyslaw , Koziarski Andrzej

Introduction: Pituitary apoplexy is a life-threatening entity developing as a result of ischemia or hemorrhage into pre-existing pituitary tumor. Clinical course is characteristic and commonly consists of severe headache accompanied by nausea, emesis, impaired consciousness, visual field impairment as well as eyeballs movement restriction. Symptoms are typically accompanied by secondary adrenal insufficiency. Corticosteroids are drugs of choice regarding coexisting adrenal ins...

ea0035p940 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Assessment of glucose homeostasis alterations, inflammatory markers, and coagulation parameters following a successful transsphenoidal surgery for Cushing's disease: preliminary report.

Witek Joanna , Witek Przemyslaw , Zielinski Grzegorz , Blazik Marlena , Kaminski Grzegorz

Background: Cortisol excess in Cushing’s disease (CD) leads to metabolic complications, thromboembolic events, and increased cardiovascular risk. The aim of this study was to assess the reversibility of glucose homeostasis alterations and dynamics of inflammatory and coagulation parameters following the successful transsphenoidal surgery.Methods: The group consisted of 14 patients with CD (11 females; age: 41.5±14.5) operated on according to th...