Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep708 | Pituitary and Neuroendocrinology | ECE2022

A Rare Case of Isolated ACTH deficiency, Possible cause: long-term use of opioid analgesics for severe Migraine management/Opioid-induced adrenal insufficiency (OIAI) (?)

Zavrashvili Nino , Chanturishvili Ketevan , Gvazava Ketevan , Margvelashvili Natia , Shonia Natia

Context: Hypothalamic-pituitary-adrenal axis (HPA) may be disrupted by drugs, including opioids. Opioids are widely used for treatment of acute and chronic pain, but they also carry a wide range of adverse effects. Opioid receptors are present in the pituitary gland and hypothalamus and chronic use of opioids may lead to adrenal insufficiency because of central suppression of the hypothalamic-pituitary-adrenal axis (HPA).Case Presentation: We report a 26...

ea0090p49 | Calcium and Bone | ECE2023

Pregnancy and Lactation Associated Osteoporosis -A Rare Case Report

Chanturishvili Ketevan , Zavrashvili Nino , Gvazava Qetevan , Margvelashvili Natia , Shonia Natia

Context: Pregnancy and lactation -associated osteoporosis (PLO) is an uncommon condition affecting women during late pregnancy and the early postpartum period. PLO is manifested with fractures usually in spine or occasionally in the hip with severe and prolonged pain and height loss. Pathogenesis of this rare condition is still not completely understood.Case Presentation: We report a 28 y/o female patient presenting with severe back pain during postpartu...

ea0090ep98 | Adrenal and Cardiovascular Endocrinology | ECE2023

Adrenal insufficiency secondary to steroid withdrawal: A Case Report

Gvazava Qetevan , Zavrashvili Nino , Chanturishvili Ketevan , Margvelashvili Natia , Shonia Natia

Introduction: Glucocorticoids are widely used for their anti-inflammatory and immunosuppressive properties. Prolonged administration of synthetic glucocorticoids is one of the most common cause of ACTH deficiency and consequent adrenal insufficiency. Exogenous glucocorticoids interfere with and suppress HPA axis and abrupt steroid withdrawal leaves body susceptible to adrenal insufficiency. Symptoms can range from adrenal crisis to nonspecific complains of fatigue, nausea and ...

ea0081ep801 | Pituitary and Neuroendocrinology | ECE2022

PE in Surgically Treated Cushing’s Disease: A Case Report

Gvazava Ketevan , Zavrashvili Nino , Chanturishvili Ketevan Shonia Natia , Margvelashvili Natia , Gvazava Qetevan , Zavrashvili Nino , Margvelashvili Natia , Shonia Natia , Chanturishvili Ketevan

Title: Pulmonary Embolism in Surgically Treated Cushing’s Disease: A Case ReportAuthors: Qetevan Gvazava1, Nino Zavrashvili1, Natia Margvelashvili2, Natia Shonia2, Ketevan Chanturishvili2 Endocrinology Department, Tbilisi Institute of MedicineBackground: Cushing’s disease is the most common cause of Cushing’s syndrome but can be very difficult to diagnose and to treat. as we know it has numerous health effects on pat...

ea0090ep897 | Pituitary and Neuroendocrinology | ECE2023

Different etiologies of the endocrine hyponatremia

Margvelashvili Natia , Shonia Natia , Zavrashvili Nino , Chanturishvili Ketevan , Gvazava Qetevan , Arjevanidze George

Hyponatremia is the most common disorder of electrolytes encountered in clinical practice, occurring in 15-30% of acutely or chronically hospitalized patients. Although many cases are mild and relatively asymptomatic, hyponatremia is nonetheless important clinically because: acute severe hyponatremia can cause substantial morbidity and mortality; overly rapid correction of chronic hyponatremia can cause severe neurological deficits and death. We present Clinical cases of endoc...

ea0081ep212 | Calcium and Bone | ECE2022

A rare case of Pseudohypoparathyroidism

Shonia Natia , Zavrashvili Nino

Background: Pseudohypoparathyroidism includes a genotypically diverse group of syndromes of primary resistance to hormones whose actions are mediated by cyclic adenosine 3’: 5’-monophosphate, in most cases caused by mutations and/or epigenetic changes at the complex GNAS locus on chromosome 20q13.3.Renal resistance to PTH leads to impaired formation of 1,25(OH)2D, the fully active form of vitamin D, and reduces expression of sodium-dependent phosphate transporters in...

ea0092ps3-25-09 | Case Reports 2 | ETA2023

Autoimmune hypothyroidism associated with pseudohypoparathyroidism

Shonia Natia , Zavrashvili Nino

Introduction: Hashimoto thyroiditis is an autoimmune disorder affecting the thyroid gland leading to chronic inflammation and gradual decline of the thyroid gland function eventually requiring hormone replacement. Patients present with classic symptoms and signs of hypothyroidism. The term pseudohypoparathryoidism (PHP) refers to a group of rare genetic and epigenetic disorders characterized by resistance to the action of parathyroid hormone (PTH) that activates cAMP signaling...

ea0081ep119 | Adrenal and Cardiovascular Endocrinology | ECE2022

A case of autoimmune polyglandular syndrome type 2

Zavrashvili Nino , Chanturishvili Ketevan , Margvelashvili Natia , Gvazava Ketevan , Shonia Natia

Autoimmune polyglandular syndromes (APS) are a group of immune-endocrine syndromes that cause autoimmune destruction of multiple endocrine organs. The most common in this group is APS type 2, which frequently presents with primary adrenal insufficiency with autoimmune thyroid disease and/or type 1 diabetes mellitus. We present a case of 46 year old male, with no significant medical history who presented in our clinic with: weakness, fatigue and weight loss for the preceding la...

ea0090ep120 | Adrenal and Cardiovascular Endocrinology | ECE2023

Primary Aldosteronism and Cortisol Cosecretion in a Patient with Adrenal Adenoma

Zavrashvili Nino , Shonia Natia , Chanturishvili Ketevan , Gvazava Qetevan , Margvelashvili Natia

Background: Primary aldosteronism (PA) is a group of disorders characterized with inappropriately high adrenal aldosterone production, suppressed renin and hypertension. Prevalence of PA is approximately 5-10% in people with hypertension and up to 20-50% in those with resistant hypertension. PA is associated with increased cardiovascular and cerebrovascular morbidity and mortality rates compared with patients with essential hypertension when matched with age, sex and blood pre...

ea0090ep789 | Pituitary and Neuroendocrinology | ECE2023

Diagnostic approach and treatment options for a geriatric patient with panhypopituitarism due to pituitary apoplexy

Shonia Natia , Chanturishvili Ketevan , Margvelashvili Natia , Zavrashvili Nino , Gvazava Qetevan

Pituitary apoplexy (PA) is a rare clinical syndrome related to abrupt hemorrhage and/or infarction of the pituitary gland, usually occurring in patients with preexisting pituitary disease. It is an endocrine emergency requiring rapid diagnosis and appropriate management. Pituitary apoplexy may lead to multiple pituitary hormone deficiencies. Without proper diagnosis and management, these can lead to the occurrence of irreversible complications, most significantly adrenal crisi...