Searchable abstracts of presentations at key conferences in endocrinology

ea0063ep7 | Adrenal and Neuroendocrine Tumours | ECE2019

Adrenal carcinoma presenting as suicidal depression

Petrescu Denisa , Georgescu Carmen Emanuela , Crisan Catalina , Silaghi Horatiu , Suciu-Petrescu Malina , Lungu Ionela , Silaghi Cristina Alina

Depression can be an early manifestation of Cushing Syndrome (CS) and found to correlate with the severity of the clinical presentation. Rates for major depression vary from 12% to 50–70%. A 37-year-old male was admitted for sad mood, affective lability, suicidal ideation without a plan and micromanian incurability ideation. The medical history of the patient revealed an old anterior-lateral myocardial infarction last year, with percutaneous coronary intervention on diago...

ea0049ep114 | Clinical case reports - Pituitary/Adrenal | ECE2017

Large adrenal adenoma presenting as a clinically inapparent Cushing syndrome, a trap diagnosis

Petrescu Denisa , Silaghi Cristina Alina , Crisan Doina , Cosma Daniel Tudor , Lungu Ionela , Georgescu Carmen Emanuela , Chira Romeo Ioan , Silaghi Horatiu

Adrenal incidentalomas (prevalence between 0.4 and 7%) have become a very common clinical problem, the major concern being the risk of malignancy and hormone overproduction.A 57-year-old woman was admitted for asthenia and uncontrolled hypertension. The only relevant clinical signs were abdominal obesity (BMI=31.1 kg/m2) and hypertension. Abdominal ultrasonography showed a voluminous left adrenal solid mass of 10/9 cm, with well-defined sharp ...

ea0049ep158 | Endocrine tumours and neoplasia | ECE2017

Bilateral pheochromocytomas, asyptomatic medullary thyroid carcinoma associated with left side thyroid hemiagenesis in a patient with MEN2A: diagnostic correlations

Lungu Ionela , Georgescu Carmen Emanuela , Ciurea Anca , Georgiu Carmen , Petrescu Denisa , Cosma Daniel Tudor , Silaghi Horatiu , Silaghi Cristina Alina

Multiple endocrine neoplasia 2A (MEN2A), an autosomal dominant genetic syndrome caused by germline mutation in RET proto-oncogene, associates medullary thyroid carcinoma (MTC), pheochromocytoma (PHEO) and primary hyperparathyroidism (HPT). Thyroid hemiagenesis (TH), the absence of one lobe, is a rare congenital abnormality (300 cases are reported in literature). Most cases of TH are diagnosed when patients present a lesion in the functioning lobe. TH was observed among members...

ea0056p94 | Clinical case reports - Pituitary/Adrenal | ECE2018

Difficult Management of Autoimmune Polyglandular Syndrome Type 1

Petrescu Denisa , Silaghi Cristina Alina , Albu Adriana , Silaghi Horatiu , Lungu Ionela , Suciu-Petrescu Malina , Bucerzan Simona , Georgescu Carmen Emanuela

Autoimmune Polyglandular Syndrome Type I (APS 1) is a rare monogenic disease, in which simultaneous or sequential dysfunctions of endocrine or nonendocrine glands appear. A 19-year-old woman was admitted for inappetence, nausea, vomiting, abdominal pain, chronic constipation, generalized paresthesia and vertigo. She was known with primary hypoparathyroidism (from the age of 5), chronic autoimmune thyroiditis, mucocutaneous candidiasis, under treatment with calcitriol, calcium,...

ea0056p225 | Calcium & Vitamin D metabolism | ECE2018

Primary hyperparathyroidism due to a parathyroid adenoma with cystic degeneration presenting as recurrent acute pancreatitis

Lungu Ionela , Silaghi Cristina Alina , Silaghi Horatiu , Cobzac Gheorghe , Nagy Georgiana , Petrescu Denisa , Mirescu Claudiu Stefan , Georgescu Carmen Emanuela

Primary hyperparathyroidism (PHPT) is rarely associated with the development of acute pancreatitis (AP). The incidence of AP induced by hypercalcemia in PHPT varies between 1.5 and 7%. PHPT is most commonly caused by parathyroid adenoma and infrequently by parathyroid hyperplasia, carcinoma or cyst and multiple endocrine neoplasia (MEN) types 1 and 2A. The present case is a 48-year-old man referred to our service for further investigation 1 month after an acute hemorrhagic nec...