Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep1149 | Late Breaking | ECE2023

Excessive production of chromogranine A in a meningioma with somatostatin receptors expression confirmed by GA68 -DOTATATE PET

Manzanares Cordova Rossana , Rodriguez Pilar

Background: Chromogranin A (CgA) is the most abundant granin in gastroenteropancreatic neuroendocrine tumors (GEP-NETs). As a tumor marker is moderately sensitive and nonspecific. Meningiomas are benign brain tumors that are usually to recur. Studies have shown in vitro and in vivo that meningiomas, regardless of histology and classification, express somatostatin receptors (SSTRs). GA68-DOTATATE PET is an exciting imaging modality that has shown significant a...

ea0090ep347 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

“We must always think that there may be something else”. Cushing’s disease and a rare partial hereditary lipodystrophy type 6 associated with retinos pigmentosis, coexistence of both diseases in a single patient

Rodriguez Pilar , Lopez Valverde Maria Eugenia , Del Can Diego Jesus

Lipodystrophic syndromes are a heterogeneous group of usually rare disorders, which have in common the selective and irreversible deficiency of adipose tissue in the absence of nutritional deprivation or catabolic state. Clinically, they are characterized by insulin resistance, related to a state of hypoleptinemia, with manifestations such as polycystic ovarian syndrome, type 2 diabetes mellitus, severe hypertriglyceridemia, and steatohepatitis among their most frequent metabo...

ea0063p476 | Calcium and Bone 2 | ECE2019

Pineal chordoid meningioma in patient with familial hypocalciuric hypercalcemia, a combination of two rare conditions: Report of a clinical case

Lopez Manuel Martin , Lloclla Eyvee Arturo Cuellar , Ortega Pilar Rodriguez , Perez Maria Isabel Rebollo

Introduction: Familial hypocalciuric hypercalcemia (FHH) is a rare condition (1–2% of causes for hypercalcemia) and may be confused with primary hyperparathyroidism. Diagnosis of FHH must be suspected in patients with a family history of chronic hypercalcemia, no symptoms and low urinary excretion. This disease is due to mutations in the calcium-sensing receptor (CASR) gene. Meningiomas are common intracranial tumors (15–20% of primary neoplasms of the central nervou...

ea0049ep1001 | Pituitary - Clinical | ECE2017

A case of pituitary apoplexy. a acute medical emergency and restitutio ad integrum

Rodriguez Pilar , Lainez Maria , Lopez Maria Jose , Roldan Eloisa , Rebollo Isabel

A 50-year-old woman with no history of interest who was admitted in hospital for progressive headache 2 weeks of evolution refractory to treatment that was accompanied by emetic syndrome and paresthesias in face and arms. A CT scan of the skull (urgency) was performed which was normal. Neurology improves with analgesia and steroids, presenting mild drowsiness and mild hyponatremia (121 mEq/l). A cerebral MRI was performed, showing a right subacute hemorrhagic adenoma of 1 cm t...

ea0022p221 | Clinical case reports and clinical practice | ECE2010

Two therapeutic approaches for thyrotropin-secreting pituitary adenomas

Sambo Marcel , Garcia Rogelio , Fernandez Elisa , Andia Victor , Lezcano Diego , Alvarez Pilar , Rodriguez Paloma

Case 1: Thirty-eight year woman consulted to gynecologist for oligomenorrhea in the last 4 years; PRL 51 μg/l and TSH 8.4 mU/l were discovered, initiating treatment with levotiroxine (f-T4). She got pregnant, persisting elevated levels of TSH and increasing f-T4, with normal campimetry. With the diagnostic of hyperthyroidism due to inadequate TSH secretion, treatment with PTU was initiated. After normal delivery, MRI showed a 22 mm. hypophisary macroadenoma and a transesp...

ea0056ep149 | Reproductive Endocrinology | ECE2018

“Gym and anabolists”

Rodriguez Pilar , Diaz Catalina , Rebollo Isabel , Gonzalez Irene , Lopez Maria Jose

This is a 38-year-old male, a regular user of a gym with the sole purpose of improving his physical performance and muscular strength and habitual consumer of hyperproteic dietary supplements. Among his PAs he denies toxic habits, and highlights the removal of the right testicle in childhood. Consultation for decreased desire and sexual potency, together with pain and turgor in the left breast; hair loss at the frontal level, in analytic carried out by the Primary Care Physici...

ea0070aep933 | Thyroid | ECE2020

Thyroid hormone resistance and succesful gestation with unaffected fetus: A case report

Eugenia López Valverde María , Manzanares Cordova Rossana , Rodriguez Pilar , Inés Velasco López María

Thyroid hormone resistance (THR) is a rare dominantly inherited syndrome characterized by a reduced response of target tissues to thyroid hormone receptor. In most cases, THR is related to mutations in the thyroid hormone receptor beta gene (THRb). Management may be challenging in cases of gestation. Here we report the case of a pregnant patient with a possible not previously described mutation and negative genotype fetus.Case report: Thirty-two year old...

ea0063p215 | Diabetes, Obesity and Metabolism 1 | ECE2019

Lipodistrophy, a rare disease: ‘If you don’t think about it, you doesn’t diagnose it’

Ortega Rodriguez Pilar , Valverde Lopez ME , Lopez Martin M , Mayorga Roldan E , Perez Rebollo I , Salas Carrasco Pilar , Vilar Araujo D

Introduction: In the geographical area of southern Spain, in the province of Huelva, we have detected prevalent cases of Dunnigan’s partial hereditary lipodystrophy. The genealogy, the suspicion phenotype and the coordination with the Genetics Service and Reference center, have borne fruit, and more and more families are detected in Our Area. The lipodystrophies, in general, are rare diseases that affect the adipose tissue, disappearance of it in different parts of the bo...

ea0063p747 | Thyroid 2 | ECE2019

Patient with graves disease and antithyroid drugs allergy: when endocrinology becomes an art

Navarro Irene Gonzalez , Lopez Maria Lainez , Valverde Maria Eugenia Lopez , Ojeda Luna Florencio , Lloclla Eyvee Arturo Cuellar , Ortega Pilar Rodriguez , Manzanares Rossanna Cordova , Martin Manuel , Mayorga Eloisa Roldan , Perez Isabel Rebollo

Introduction: First treatment in Graves’ disease consists in the administration of antithyroid drugs. The most common side effect is a rash, which affects about 5% patients and clears up if the drug is stopped. The other drug may then be used. The intolerance to both drugs is very rare, but in this situation early radioactive iodine or surgery may be the answer.Case report: Woman of 61 years old who developed primary hyperthiroidism, with levels of ...