Searchable abstracts of presentations at key conferences in endocrinology

ea0081p745 | Thyroid | ECE2022

Myxedema coma of both primary and secondary origin, with non-classic presentation and elevated creatine kinase

Lucian Pavel Mihai , Sirbu Anca Elena , Maria Popa Miruna , Bargaoanu Irina , Fica Simona

Introduction: Myxedema coma is the end stage of untreated or inadequately treated hypothyroidism. It has an estimated incidence of 0.22 per million per year. The clinical picture is often that of an elderly obese female, presenting in midwinter with increased lethargy, somnolence and confusion. The presentation is one of severe hypothyroidism, with or without coma.Such cases are predominantly based on a primary thyroid disorder such as Hashimoto′s ...

ea0081ep127 | Adrenal and Cardiovascular Endocrinology | ECE2022

A newly diagnosed Cushing’s syndrome after a visit at the Emergency Department

Iliescu Marina , Tarna Mihaela , Andrei Marian , Cima Luminita Nicoleta , Martin Carmen Sorina , Simona Fica

Cushing’s syndrome results from an excess exposure to glucocorticoids which can result from various causes, divided into ACTH-dependent and ACTH-independent etiologies. An example of ACTH-independent causes are adrenal masses which are either benign adenomas, representing the majority of adrenal mass cases, or by malignant neoplasms. We present the case of a 52 yo woman who presented at the Emergency Department (ER) with thoracic pain and palpitations, for which several c...

ea0081ep719 | Pituitary and Neuroendocrinology | ECE2022

FSH- secreting pituitary microadenoma and ovarian hyperstimulation

Andrei Marian , Cima Luminita Nicoleta , Tarna Mihaela , Iliescu Marina , Simona Fica

Introduction: The prevalence of functioning gonadotropinoma is difficult to assess since most of reports are case reports. Gonadotropinomas rarely lead to a noticeable clinical syndrome. They usually produce symptoms associated with mass effect such as headaches, visual field impairment and hormonal deficiencies.Case report: We present the case of a 38 years old women diagnosed in 2017 with microprolactinoma. She had elevated prolactin level (108 ng/ml) ...

ea0081ep781 | Pituitary and Neuroendocrinology | ECE2022

Discordant GH and IGF-1 values in a surgically treated acromegaly patient: a management conundrum

Mustata Theodor , Martin Carmen Sorina , Parfeni Ovidiu , Dumea Bianca , Predescu Florina Andrada , Simona Fica

Introduction: Remission after transsphenoidal surgery in patients with acromegaly is confirmed by biochemical assays of growth hormone (GH) and insulin-like growth factor-1 (IGF-1). Although their levels are usually closely correlated, discordant results of these tests have been noted, making the follow-up of acromegaly patients particularly challenging.Case report: We present the case of a 35 year old female diagnosed with acromegaly at the age of 32 ye...

ea0081ep1061 | Thyroid | ECE2022

Horner syndrome as the first manifestation of medullary thyroid cancer

Dumea Bianca , Martin Carmen Sorina , Parfeni Ovidiu , Mustata Theodor , Predescu Florina Andrada , Simona Fica

Introduction: Medullary thyroid cancer is a rare neuroendocrine tumor arising from the parafollicular C cells of the thyroid gland. Calcitonin production is a characteristic feature of medullary thyroid cancer and preoperative high levels indicate an increased risk of local and distant metastatic disease. Although rare, Horner syndrome could be caused by metastatic medullary thyroid cancer. Horner syndrome usually presents with ptosis, miosis and facial anhidrosis and most of ...

ea0084ps3-11-103 | Case Reports | ETA2022

Suspicious thyroid nodule in de quervain’s thyroiditis

Sorina Martin Carmen , Dumea Bianca , Parfeni Ovidiu , Mustata Theodor , Sirbu Anca , Fica Simona

Introduction: De Quervain’s thyroiditis, also known as subacute granulomatous thyroiditis, is a self-limiting inflammatory disorder of the thyroid gland. It is presumed to be caused by a viral infection and many patients have a history of an upper respiratory infection 2-8 weeks prior to the onset of thyroiditis. It is the most common cause for neck pain or discomfort, and it usually has a predictable course of thyroid function evolution. On ultrasonography the thyroid gl...

ea0086p26 | Adrenal and Cardiovascular | SFEBES2022

Primary adrenal lymphoma as the culprit of fever of unknown origin and adrenal insufficiency

Martin Sorina , Mustata Theodor , Dumitru Parfeni Ovidiu , Ciobanu Carla , Fica Simona

Introduction: Primary adrenal lymphoma is a rare cause of adrenal insufficiency, with most cases being of B-cell lymphoma.Case report: We present the case of a 51 yo man with a 1.5-month history of recurrent fever, nausea, vomiting, anorexia, weight loss of 12 kg, fatigue, polyarthalgia, hypotensive episodes (70/40 mmHg) and singultus. Before admission in our clinic he had a thoracic CT scan, which showed a 5.5 cm right adrenal mass and hyperplasia of th...

ea0086p215 | Metabolism, Obesity and Diabetes | SFEBES2022

Metabolic syndrome and obesity in IBD patients: how common?

Soare Iulia , Sirbu Anca , Diculescu Mircea , Radu Mateescu Bogdan , George Tieranu Cristian , Martin Sorina , Fica Simona

Introduction: Although patients with inflammatory bowel disease (IBD) -Crohn’s disease (CD) and ulcerative colitis (UC)- are considered prone to malnutrition, studies have shown an increased risk for obesity, especially visceral obesity and metabolic syndrome (MetS). Possible mechanisms involved include dysbiosis, gut microbiome and chronic inflammation. The aim of the study was to assess the prevalence of MetS and obesity in a group of IBD patients.<p class="abstext"...

ea0090ep66 | Adrenal and Cardiovascular Endocrinology | ECE2023

Overview and factors that impact quality of life in patients with Cushing’s syndrome

Nacu Miruna-Viorela , Martin Carmen Sorina , Sirbu Anca , Barbu Carmen , Fica Simona

Background: Quality of life (QoL) has become a useful outcome in recent studies among different specialties. In Cushing’s syndrome, elevated cortisol levels result in a decreased QoL, the cause for this impairment being multifactorial. More studies are necessary to find modifiable factors where doctors could intervene and thus improve QoL.Objective: To evaluate QoL in a group of Romanian patients with Cushing’s syndrome. Design: We performed a ...

ea0090ep637 | Endocrine-related Cancer | ECE2023

Neuroendocrine carcinoma of the vagina in a young patient – a rare entity

Duta Simona Gabriela , Dumitras Teodor , Sorina Martin Carmen , Cima Luminita , Nitipir Cornelia , Terzea Dana , Fica Simona

Primary vaginal malignancy is uncommon, accounting for about 2% of all gynecological tract cancers, with small-cell neuroendocrine carcinoma of the vagina being exceptionally rare and aggressive. They display similar histological and immunohistochemical features to small-cell carcinomas of different origin. Few cases are reported in the literature so far and therefore, there is no current treatment protocol consensus. We report the case of a 34-year-old nulliparous patient, wh...