Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep1209 | Clinical case reports - Thyroid/Others | ECE2017

Autoimmune thyroid disease occurring as a possible late complication after a non-occupational HIV Postexposure Prophylaxis

Crumpei Iulia , Mogos Voichita , Ungureanu Maria-Christina , Bursuc Anamaria , Armasu Ioana , Tirnoveanu Mirela , Adomnicai Valentina , Constantinescu Georgiana , Vulpoi Carmen

Introduction: Nonoccupational postexposure prophylaxis (nPEP) is a three-drug antiretroviral regimen used to decrease the risk for HIV infection after less than 72 h from nonoccupational exposure to body fluids that might contain HIV. The most frequent side effects concern the gastro-intestinal intolerance, renal and hepatic toxicity, with no hormonal imbalance to have been yet reported.Case report: 24 years old male patient, consulted for palpitations, ...

ea0041ep337 | Clinical case reports - Thyroid/Others | ECE2016

Management dilemma in papillary carcinoma arising from struma ovarii

Hreniuc Ana , Gherasim Simona , Preda Cristina , Ungureanu Maria-Christina , Vulpoi Carmen , Mogos Voichita , Piciu Doina , Danila Radu , Leustean Letitia

A rare ovarian teratoma consisting mainly of thyroid tissue, Struma ovarii accounts for up to 3% of all ovarian tumors. The thyroid tissue may demonstrate the same spectrum of pathological features as in the normal thyroid including benign and malignant changes.A 46-year-old woman was referred to our clinic in July 2015 by the oncologist, with the diagnosis of struma ovarii with carcinomatous transformation (follicular variant of papillary carcinoma).</p...

ea0037ep1218 | Clinical Cases–Pituitary/Adrenal | ECE2015

Rare aetiology for primary adrenal failure: ACTH resistance

Hristov Ioana , Gherasim Simona , Hreniuc Ana , Ungureanu Maria Christina , Preda Cristina , Vulpoi Carmen , Mogos Voichita , Leustean Letitia

Introduction: ACTH resistance syndromes are rare, autosomal and genetically heterogeneous diseases that include familial glucocorticoid deficiency and triple A syndrome. These are characterised by early onset of primary adrenocortical insufficiency associated with hypoglycaemia, convulsions and skin pigmentation.Case report: We present the case of primary adrenal failure in a boy diagnosed at the age of four, during a decompensation episode with hypoglyc...

ea0037ep1343 | Clinical Cases–Thyroid/Other | ECE2015

Concomitance of pancreatic and neuroendocrine breast tumour – simple coincidence or not?

Crumpei Iulia , Fadur Alina , Manolachie Adina , Zmau George , Anton Mihaela , Volovat Constantin , Ungureanu Maria Christina , Vulpoi Carmen

Introduction: Breast neuroendocrine carcinoma is a rare aggressive neuroendocrine tumour (NET) and the research on this subject is poor. Only seven studies were cited in the literature. Incidence in the population has not been reported, but the prevalence is under 0.1% of all breast carcinomas.Case report: AV, 72, is hospitalised for bone pain and significant weight loss (15 kg in 2 months). Patient’s previous history are: diabetes, hypertension, no...

ea0035p246 | Clinical case reports Pituitary/Adrenal | ECE2014

Prepubertal male gynecomastia-issues of diagnosis

Hreniuc Ana , Gherasim Simona , Hristov Ioana , Preda Cristina , Vulpoi Carmen , Ungureanu Maria-Christina , Cristea Cristina , Mogos Voichita , Leustean Letitia

We present the case of 13 years old boy referred to our service in June 2013 for bilateral gynecomastia (appeared for ~1 year). The boy’s father presented delayed puberty (at 18-year-old). No other pathological hereditary conditions were reported.Clinical examination revealed: gynoid status with height =167 cm (−1.4 DS), weight=63.5 kg, important bilateral gynecomastia with hypo pigmented areola and painful palpation. Sexual development was PI...

ea0070ep11 | Adrenal and Cardiovascular Endocrinology | ECE2020

A case of coexisting carotid body paraganglioma, adrenal incidentaloma and malignant peripheral nerve sheath tumor. Coincidence or something more?

Neagu Georgiana , Ungureanu Maria-Christina , Iftimie-Gavrilas Irina , Teodoriu Laura , Rosu Andreea , Chiriac Bianca , Protop Madalina , Chelaru Alina , Preda Cristina

Introduction: Paraganglioma (PGL) is a neuroendocrine tumor (NET) originating from the neural crest cells. Head and neck paraganglioma (HNPGL) often presents as an asymptomatic slow growing tumor and is rarely functional. Adrenal incidentaloma (AI) is defined as a silent adrenal mass detected on imaging performed for unrelated disorder. Malignant peripheral nerve sheath tumor (MPNST) is a variety of soft tissue sarcoma derived from cells of neural crest....

ea0070ep46 | Adrenal and Cardiovascular Endocrinology | ECE2020

Metastatic melanoma of unknown primary lesion presenting as bilateral adrenal incidentalomas

Anisia Miruna , Teusan Teodora , Ciobotar Mihaela , Preda Cristina , Ungureanu Maria Christina , Danciu Mihai , Lupascu Cristian , Leustean Letitia

Introduction: Bilateral adrenal incidentalomas represent a challenge both in diagnosis and therapeutic approaches. While initial testing is similar to unilateral adrenal incidentalomas, additional investigations should be made considering the differences between the distribution of etiologies.Case report: We report the case of a 67 years old hypertensive female, presenting with backpain; an initial abdominal ultrasound described left adrenal mass and a l...

ea0022p231 | Clinical case reports and clinical practice | ECE2010

Isolated parietal-skull metastasis from a thyroid papillary carcinoma

Preda Cristina , Novac Roxana , Ciobanu Delia , Grigorovici Alexandru , Leustean Letitia , Ungureanu Maria-Christina , Cristea Cristina , Zbranca Eusebie

Papillary carcinoma is the most common differentiated malignant thyroid neoplasm. Metastasis commonly occur in regional lymph nodes and distant metastasis ia a late and rare occurrence.Papillary thyroid carcinoma with metastasis to the parietal skull is very rare.We present the case of a parital skull metastasis arising from a papillary carcinoma prior to the diagnosis of thyroid tumor. The patient was a 58 caucasian woman with pre...

ea0022p860 | Thyroid | ECE2010

Thyroid incidentaloma: palpable problems of an impalpable nodule

Vulpoi Carmen , Mogos Voichita , Ciobanu Delia , Preda Cristina , Cristea Cristina , Ungureanu Maria-Christina , Leustean Letitia , Zbranca Eusebie

The widespread of sensitive imaging methods have substantially increased the incidental finding of subclinical thyroid nodules. The ‘epidemic’ of thyroid incidentaloma has raised numerous discussions regarding their management: Is it necessary to investigate all nodules or is surveillance sufficient? Which criteria should be used in order to identify the nodules which must be investigated by fine-needle aspiration (FNA) (size, echogenicity, vascularisation)? Should w...

ea0020p292 | Clinical case reports and clinical reports | ECE2009

Clinical analysis of 150 patients with pituitary insufficiency (20 years experience)

Preda Cristina , Leustean Letitia , Ungureanu Maria-Christina , Cristea Cristina , Mogos Voichita , Galesanu Corina , Vulpoi Carmen , Zbranca Eusebie

Background: Pituitary insufficiency is an uncommon endocrine disorder (incidence 2–4 per 100 000 per year), which clinical symptoms depend on the degree of hormone depletion and the rapidity of onset.Aim: To determine the clinical presentation, aetiology and clinical forms in 150 patients diagnosed with pituitary insufficiency.Material and methods: Retrospective study of clinical records of 150 patients with pituitary insuffic...