Searchable abstracts of presentations at key conferences in endocrinology

ea0011p925 | Thyroid | ECE2006

Thyrotoxicosis is coupled with quantitative and qualitative sleep disruptions

Riganti F , Prodam F , Gramaglia E , van Cauter E , Ghigo E , Broglio F

Despite the common clinical opinion that thyrotoxicosis is associated with quantitative and qualitative sleep alterations, at present, an objective evaluation of sleep quality and quantity in this clinical condition has never been performed so far. Based on this foregoing, in order to perform a qualitative and quantitative description of sleep in this clinical condition, we enrolled 6 normal-weighted patients suffering from naïve overt hyperthyroidism due to Basedow Disea...

ea0003p20 | Clinical Case Reports | BES2002

A rare cause of intrasellar mass: Cholesterol granuloma

Kelestimur F , Unluhizarci K , Colak R , Balkanli S , Karahan I , Selcuklu A , Ozturk F , Bayram F

The most common cause of a mass lesion in the sella is pituitary adenoma. Some parasellar lesions may be cystic and sometimes may mimic the clinical and radiological features of pituitary adenoma. A 36 year-old woman was admitted to the hospital because of headache for five years and amenorrhoea for five months. Magnetic resonance (MR) imaging of the pituitary gland showed sellar mass lesion characterized by high signal intensity on T1 and T2-weighted images. Endocrinological ...

ea0049ep389 | Clinical case reports - Thyroid/Others | ECE2017

Improved xanthomas after leptin replacement short therapy in congenital lipodystrophy patient

Oliveira-Filho Antonio F , Dantas Irla A , Velloso Renata N , de Oliveira Sofia N P , Candido Diego F F , Nunes Adriana

Berardinelli-Seip syndrome is an autosomal recessive disorder characterized by generalized lipoatrophy, extreme insulin resistance with dyslipidaemia in childhood and development of diabetes and hepatic steatosis in adolescence. The metabolic derangements can be severe and lead to substantial comorbidities, including acute pancreatitis, hepatic cirrhosis, and premature cardiovascular disease. Other manifestations can include polycystic ovarian syndrome, acanthosis nigricans, a...

ea0029p52 | Adrenal cortex | ICEECE2012

Efficacy of long-term treatment with retinoic acid in patients with Cushing’s disease

Giraldi F. Pecori , Ambrogio A. , Andrioli M. , Sanguin F. , Karamouzis I. , Corsello S. , Scaroni C. , Arvat E. , Pontecorvi A. , Cavagnini F.

Cushing’s disease, i.e. cortisol excess due to an ACTH-secreting pituitary adenoma, is a rare disorder with considerable morbidity and mortality. Current therapeutic strategies include pituitary surgery, radiation, adrenalectomy and medical treatment with steroidogenesis inhibitors, as drugs aimed at the pituitary adenoma are as yet under investigation. Experimental data showed that retinoic acid restrains ACTH secretion by tumoral corticotrophes thus we decided to evalua...

ea0029p323 | Cardiovascular Endocrinology and Lipid Metabolism | ICEECE2012

Coronary flow reserve is inversely related to urinary cortisol in Cushing’s syndrome

Fallo F. , Capizzi D. , Dassie F. , Sonino N. , Martini C. , Paoletta A. , Famoso G. , Iliceto S. , Tona F.

There is evidence for a strong association between Cushing’s syndrome, characterized by a cluster of systemic complications, and increased cardiovascular risk. To our knowledge, coronary circulatory function has not been explored in Cushing’s syndrome. The aim of the study was to evaluate coronary flow reserve (CFR), an index of coronary microvascular function, in patients with Cushing’s syndrome. Thirteen newly diagnosed patients with Cushing’s syndrome (1...

ea0029p1122 | Neuroendocrinology | ICEECE2012

Ten years of gastroenteropancreatic neuroendocrine tumours: evolution of the classification and correlation with follow-up in 50 patients

Albertelli M. , Grillo F. , Giannone A. , Mastracci L. , Annunziata F. , Arvigo M. , Minuto F. , Fiocca R. , Ferone D.

Gastroenteropancreatic (GEP) neuroendocrine tumours (NETs) are rare neoplasms with heterogeneous clinical behavior and potential long-term survival. In the last decade GEP–NET nomenclature has been twice reviewed. However, the 2000 WHO classification had poor prognostic power in well differentiated (WD) neoplasms. This led to the introduction of two new important parameters by the European Neuroendocrine Tumors Society (ENETS), grade and stage; the former became part of t...

ea0029p1394 | Pituitary Clinical | ICEECE2012

Evaluation of ejaculatory function in acromegalic men: preliminary study

Galdiero M. , Vitale P. , Grasso L. , Lo Calzo F. , Cariati F. , Lotti F. , Maggi M. , Colao A. , Pivonello R.

Introduction: Acromegaly is a systemic disease frequently characterized by hypogonadotropic hypogonadism, endothelial dysfunction and diseases classically associated with an increased incidence of erectile dysfunction (ED) (hypertension, dyslipidemia, impaired glucose metabolism) and premature ejaculation (prostatic disease). Furthermore, the high prevalence of ED may negatively affect ejaculatory function. The purpose of this study was to evaluate the ejaculatory function of ...

ea0029p1395 | Pituitary Clinical | ICEECE2012

Evaluation of male sexual function in active acromegalic patients and after disease remission: preliminary study

Galdiero M. , Vitale P. , Grasso L. , Lo Calzo F. , Cariati F. , Lotti F. , Maggi M. , Colao A. , Pivonello R.

Introduction: Acromegaly is frequently characterized by hypogonadotropic hypogonadism, endothelial dysfunction, hypertension and impaired glucose and lipid metabolism, classically associated with impaired sexual function (SF). There are no literature data on the SF in acromegaly. The purpose of this study was to evaluate the SF of patients with acromegaly.Patients and methods: Twenty-two patients (47.8±8.6 years) were enrolled into the study. Among ...

ea0029p1767 | Thyroid cancer | ICEECE2012

Differentiated carcinoma in dysembriogenetic thyroid lesions

Sturniolo G. , Violi M. , Presti S. , Moleti M. , Di Bella B. , Di Mauro F. , Trimarchi F. , Vermiglio F.

The prevalence of differentiated thyroid carcinoma (DTC) in lingual thyroid (LT) and thyroglossal duct cysts (TDC) is around 1%. Nowadays, almost 200 cases of DTC were reported in TDC and <60 cases in LT. Here we report four cases of neoplasia in LT (1/4) and TDC (3/4) in a consecutive series of 950 DTC patients (0.4%).Case 1: D.F. 63 year-old woman with thyroid follicular carcinoma in ectopic gland located at her tongue’s basis. March 2009: the...

ea0011p41 | Bone | ECE2006

Brown tumors in hyperparathyroidism may be mistaken for primitive bone neoplasia: report of two cases

Rota CA , Ingraudo F , Paragliola RM , Ricciato MP , Bilotta AL , Ianni F , Gallo F , Ubertini G , Corsello SM , Pontecorvi A

Primary hyperparathyroidism is characterized by abnormal PTH secretion from one or more hyperfunctioning parathyroids and hypercalcemia. PTH exerts a catabolic effect on the cortical bone resulting in the osteitis fibrosa cystica. Two patients were referred to us after destroyed surgery for brown tumors mistaken for primitive bone tumors.A 59 years old man was referred to emergency department for a pathologic fracture of the left hip. The X-ray showed a ...