Searchable abstracts of presentations at key conferences in endocrinology

ea0050ep099 | Reproduction | SFEBES2017

Extremely low HDL-C in a patient with premature ovarian failure: case presentation

Hilma Ana Maria , Gogoi Adriana

During menopause, plasma lipids change in an unfavourable way to a more atherogenic pattern with, increased total and LDL-cholesterol and decreased HDL cholesterol concentrations. Women with POI show increased cardiovascular morbidity and mortality regardless of the cause of the ovarian insufficiency. The treatment of premature ovarian failure in patients presenting extremely low HLD-C is a real challenge.We present the case of a 29 ye...

ea0050ep099 | Reproduction | SFEBES2017

Extremely low HDL-C in a patient with premature ovarian failure: case presentation

Hilma Ana Maria , Gogoi Adriana

During menopause, plasma lipids change in an unfavourable way to a more atherogenic pattern with, increased total and LDL-cholesterol and decreased HDL cholesterol concentrations. Women with POI show increased cardiovascular morbidity and mortality regardless of the cause of the ovarian insufficiency. The treatment of premature ovarian failure in patients presenting extremely low HLD-C is a real challenge.We present the case of a 29 ye...

ea0065p442 | Thyroid | SFEBES2019

Multiple Mieloma associated with Graves disease – case presentation

Enachescu Iulia , Hilma Ana Maria , Gogoi Adriana

Although it is well known that aplastic anemia and agranulocytosis are potential lethal adverse reactions of antithyroid treatment, we present a case of methimazole administration in a patient with bone marrow transplant for multiple myeloma, with favorable evolution. We present the case of a 43 y.o. male, known with Grave’s disease since 2010 (on ATS treatment for only 6 months), vitiligo, systemic sclerosis and type 1 diabetes, diagnosed with multiple mieloma Ig G Tipe,...

ea0050ep094 | Reproduction | SFEBES2017

Secondary amenorrhea due to abnormalities of the autosomal chromosomes – Case report

Gogoi Adriana , Hilma Ana Maria , Popa Oana , Procopiuc Camelia

Introduction: Follicle-stimulating hormone (FSH) and its corresponding receptor (FSHR) are essential factors for regular gonadal development, sexual maturation at puberty and gamete production during the fertile period in both sexes. The FSHR encoding gene was mapped to the short arm of chromosome (CR) 2 in 2p16.3.3 In females, inactivating mutations result clinically – depending on the degree of inactivation – in primary amenorrhea, sec...

ea0050ep094 | Reproduction | SFEBES2017

Secondary amenorrhea due to abnormalities of the autosomal chromosomes – Case report

Gogoi Adriana , Hilma Ana Maria , Popa Oana , Procopiuc Camelia

Introduction: Follicle-stimulating hormone (FSH) and its corresponding receptor (FSHR) are essential factors for regular gonadal development, sexual maturation at puberty and gamete production during the fertile period in both sexes. The FSHR encoding gene was mapped to the short arm of chromosome (CR) 2 in 2p16.3.3 In females, inactivating mutations result clinically – depending on the degree of inactivation – in primary amenorrhea, sec...

ea0044ep52 | (1) | SFEBES2016

Adrenal carcinoma, a rare incidental finding: case presentation

Hilma Ana Maria , Gogoi Adriana , Jercalau Simona , Badiu Corin

Adrenal carcinoma is a very rare malignancy accounting for 0.05–0.2% of all cancers, with an incidence 0.5–2/106.We present the case of a 60 year old woman with impaired fasting glucose and hypertension, who was incidentally diagnosed, after a non-enhanced abdominal CT, with a right adrenal tumor of 4.5/6 cm. The mass was described as having smooth borders, and a heterogeneous aspect including solid parts, necrotic areas and 1 microc...

ea0044ep53 | (1) | SFEBES2016

Common Features of Giant Prolactinoma and Paranasal Neuroendocrine Carcinoma-Case Report

Gogoi Adriana , Radomir Lidia , Hilma Ana Maria , Stancu Cristina , Picu Maria , Jercalau Simona , Badiu Corin

Giant prolactinoma it’s a very rare tumor that due to its massive extension into surrounding structures can present more often with neurological complications such as visual defects, cranial nerve paresis or even hydrocephalus, unlike the classic prolactinoma presentation with amenorrhea, infertility and galactorrhea. On CT/MRI exams it can present as aggressive skull base tumor and its immunohistochemistry (IHC) may have common features with neuroendocrine neoplasms....

ea0059ep70 | Neoplasia, cancer & late effects | SFEBES2018

MEN 2A – a rare syndrome with variable intrafamilial gene expressivity, case presentation

Hilma Ana Maria , Gogoi Adriana , Jercalau Simona , Dumitrascu Anda , Goldstein Andrei , Badiu Corin

MEN2A is an autosomal dominant inherited syndrome, caused by a gain of function germline mutation in the RET proto-oncogene, with multiglandular tumoral development. Although the presence of MTC is very high and 50% of patients present with pheochromocytoma, the penetrance of hyperparathyroidism is estimated to be between 9 and 34%. The clinical presentation of the syndrome varies widely even in members of the same family, because of the difference of gene penetration (1). In ...

ea0038p339 | Pituitary | SFEBES2015

Frontal bone recurrent ectopic craniopharyngioma after transfrontal resection: case report

Hilma Ana Maria , Codreanu Ana-Maria , Stoica Sergiu , Badiu Corin , Procopiuc Camelia

Craniopharyngiomas are rare solid or mixed solid-cystic tumours. Although benign histologically, these tumours frequently shorten life and should be considered low-grade malignancies.We present the case of a 12-year-old boy diagnosed in 2008, at age 5, with a suprasellar tumour of 22/21/20 mm with mixed solid and cystic areas. The tumour was operated twice by left transfrontal approach in 2008 and right transfrontal approach in 2009. The pathology exam r...