Searchable abstracts of presentations at key conferences in endocrinology

ea0083tp5 | Thyroid | EYES2022

Autoimmune hyperthyroidism relapse with active severe Graves’ orbitopathy during second trimester of pregnancy, and thyrotoxicity development in offspring

E. Spaka

Background: Graves’ disease exacerbations during pregnancy usually occur in the first trimester with very rare cases of disease manifestation or relapse in second/third trimester. Up to five percent of neonates that are born to women with diffuse toxic goiter develop symptoms of hyperthyroidism because of transplacental transfer of TSH-receptor autoantibodies.Case presentation: Female, born in year 1990, with a history of symptomatic autoimmune hype...

ea0032s14.3 | Clinical care of the pheochromocytoma patient | ECE2013

Treatment of malignant pheochromocytomas and paragangliomas

Baudin E

Pheochromocytomas and paragangliomas are rare neuroendocrine chromaffine tumors located in the adrenal or extra-adrenal sites, respectively. Malignant pheochromocytomas or paragangliomas represent 10–20% (MPP) of these patients and are defined by the presence or occurrence of metastasis, in non chromaffin organs. MPP are characterized by their heterogeneous presentation as testified by their variety in primary locations, levels and type of hormone secretions, percentage o...

ea0029pl5 | Why your bones break - from childhood to old age | ICEECE2012

Why your bones break: from childhood to old age

Seeman E.

Bone’s ability to tolerate loading is determined by its material composition and structural design. During growth, growth plate trabeculae condense by appositional growth forming the metaphyseal cortices (‘corticalization’). Rapid distal radial longitudinal growth in early puberty outpaces trabecular condensation producing transitory intracortical porosity predisposing to fractures.In adulthood, remodeling removes and replaces damaged bone...

ea0029s15.1 | Adrenal cancer | ICEECE2012

Molecular pathogenesis of adrenocortical cancer

Lalli E.

Adrenocortical carcinoma is a rare heterogeneous neoplasm with a poor prognosis. Most patients present with symptoms related to steroid hormone excess or presence of an abdominal mass, while less frequently they are diagnosed incidentally during clinical exploration for other causes. In children, adrenocortical tumors are most commonly found associated with mutations of the TP53 tumor suppressor gene and have the highest incidence in southern Brazil. Several clinical and patho...

ea0029s30.1 | New developments in pituitary adenomas | ICEECE2012

Symposium 30: new developments in pituitary adenoma cytokines and other new genes in pituitary adenomas

Arzt E.

With the aim of identifying genes involved in the development of pituitary tumors, we used the mRNA differential display technique comparing tumor and normal pituitary cells. Two genes have been identified to be involved in pathogenesis process: in prolactinomas obtained from Dopamine D2R knockout female mice, we have found differential expression of the cytokine BPMP-4 and in clones of the tumoral lactosomatroph cell line GH3 cell line overexpressing the cytokine IL6 signal t...

ea0029s47.3 | Cushing's syndrome | ICEECE2012

Learnings from ERCUSYN: the first 500 patients

Valassi E.

The European Registry on Cushing’s syndrome (ERCUSYN) is a project aimed at gathering data at EU level on clinical features, diagnostic procedures and therapeutic strategies in CS patients. The creation of this large European database is expected to provide comprehensive information on all stages of the disease from the first diagnosis to long-term follow-up. This ultimately should result in earlier recognition of CS and all its co-morbidities, and assist clinicians in co...

ea0029p369 | Clinical case reports - Pituitary/Adrenal | ICEECE2012

A rare case of primary tubercular pituitary abscess in a diabetic patient

Madronio E.

Introduction: Primary tubercular pituitary abscess is an extremely rare disease. Only few cases had been reported and the diagnosis was reached only after surgery. There is a need to distinguish between a tuberculoma, pituitary abscess and other functioning and nonfunctioning pituitary adenoma to direct our management into either medical or surgical management, especially here in the Philippines where tuberculosis is an endemic disease.Case: We present a...

ea0026gh1 | The Geoffrey Harris Prize Lecture | ECE2011

Ghrelin: a neuroendocrine and/or a metabolic story?

Ghigo E

The acylated form of ghrelin (GRLN) was discovered as the natural ligand of the GHS-R1a. GRLN is acylated by a specific octanoyl-transferase (GOAT) and is predominantly produced by the stomach, although expressed by many other endocrine and non-endocrine, peripheral and central tissues. Also GHS-R1is widely expressed by several central and peripheral tissues. Acylated GRLN displays strong GH-releasing activity but is not specific for GH exhibiting other neuroendocrine actions ...

ea0019p18 | Bone | SFEBES2009

Renal bone disease control: comparison between diabetics and non diabetics in 187 haemodialysis patients

Panteliou E

Objectives: To compare the diabetic (DM) (n=124) and non diabetic (nonDM) (n=63) patients on haemodialysis (HD) in terms of renal bone disease (RBD) control.Methods: Retrospective case-note review of 187 HD patients. The National Kidney Foundation guidelines for chronic kidney disease stage 5 (CKD-5) were used, with target levels for parathormone (PTH) 16.5–33 pmol/l, calcium 2.1–2.35 mmols/l and phosphate 1.78 mmols/l.<p clas...