Searchable abstracts of presentations at key conferences in endocrinology

ea0086p215 | Metabolism, Obesity and Diabetes | SFEBES2022

Metabolic syndrome and obesity in IBD patients: how common?

Soare Iulia , Sirbu Anca , Diculescu Mircea , Radu Mateescu Bogdan , George Tieranu Cristian , Martin Sorina , Fica Simona

Introduction: Although patients with inflammatory bowel disease (IBD) -Crohn’s disease (CD) and ulcerative colitis (UC)- are considered prone to malnutrition, studies have shown an increased risk for obesity, especially visceral obesity and metabolic syndrome (MetS). Possible mechanisms involved include dysbiosis, gut microbiome and chronic inflammation. The aim of the study was to assess the prevalence of MetS and obesity in a group of IBD patients.<p class="abstext"...

ea0059ep36 | Bone and calcium | SFEBES2018

Low bone mass in young patient with Crohn disease: to treat or not to treat?

Soare Iulia , Sirbu Anca , Tieranu Cristian , Ionescu Mirela , Fica Simona

Introduction: Decreased bone mass is associated with inflammatory bowel disease (IBD), due to multiple factors, including endocrine disturbances, deficits in calcium and vitamin D, malnutrition, drugs (corticosteroids), chronic inflammation. If in older man and postmenopausal women, the treatment is well established, for young patients is not a general consensus.Case report: We report the case of a 20-year-old, male, nonsmoker, diagnosed with Crohn disea...

ea0025p46 | Clinical biochemistry | SFEBES2011

A case of Di George’s syndrome presenting in late adulthood

Brewster Sarah , Rajendran Rajesh , Coppini David , Richardson Tristan

Introduction: Di George’s syndrome is a rare congenital disease that is usually diagnosed in childhood due to its presentation with velo-cardio-facial abnormalities.Case report: A 42-year-old man was incidentally found to be hypocalcaemic (corrected calcium 1.71 mmol/l) during a ‘well-man check’. A subsequent parathyroid hormone (PTH) was inappropriately low at 0.8 pmol/l (reference range 0.5–4.4 pmol/l).He was ...

ea0013p45 | Clinical practice/governance and case reports | SFEBES2007

Di-George syndrome presenting as hypocalcaemia in adulthood

Hunter Steven , Johnston Philip , Morrison Patrick

A 29 year old female presented with a two year history of recurrent numbness and tingling in her hands. Trousseau’s sign was positive. Investigations confirmed hypocalcaemia with serum calcium 1.64 nmol/L (2.10–2.60), phosphate 1.23 nmol/L (0.80–1.55), alkaline phosphatase 82 U/L (35–120). Parathyroid hormone was inappropriately normal at 36 pg/ml (10–65), Vitamin D 78 nmol/L (50–75). Her mother reported a history of hypocalcaemia when she was two...

ea0077p34 | Bone and Calcium | SFEBES2021

Vitamin D deficiency and inflammation in IBD patients

Soare Iulia , Sirbu Anca , Diculescu Mircea , Mateescu Bogdan Radu , Tieranu Cristian , Cima Luminita , Fica Simona

Introduction: Vitamin D is a potential immune modulator and low levels are common in inflammatory bowel disease (IBD) patients. The aim of the study was to determine the association between deficient vitamin D and inflammatory profile.Methods: Intestinal (fecal calprotectin) and blood inflammatory profile [erythrocytes sedimentation rate (ESR), protein C reactive, fibrinogen], were performed to all patients. In addition, level of 25 hydroxy vitamin D was...

ea0065p82 | Bone and calcium | SFEBES2019

Association between lean mass and bone mass density in patients with inflammatory bowel disease

Soare Iulia , Sirbu Anca , Mateescu Bogdan Radu , Martin Sorina , Tieranu Cristian , Diculescu Mircea , Fica Simona

Introduction: Patients with inflammatory bowel disease (IBD) are at increased risk for decreased bone mass density (BMD), fractures. Preserved muscle mass is important for healthy bones. Low mean mass can be found in these patients due to immobilization, lack of physical activity and glucocorticoids. Our aim was to evaluate the presence of low BMD and muscle mass impact on it.Methods: 64 patients with inflammatory bowel disease (40 with Crohn disease, 24...

ea0070aep536 | Endocrine-related Cancer | ECE2020

Real medical challenges in the diagnostic of gastrinomas

Alexandra Ciobanu Oana , Tieranu Cristian , Terzea Dana , Nistor Irina , Mitrache Marius , Simona Fica

Introduction: Chronic hypergastrinemia is no longer an uncommon phenomenon. Zollinger-Ellison syndrome [ZES], chronic atrophic gastritis [CAG] type A, proton pump inhibitors [PPI] therapy, or Helicobacter pylori-induced CAG type B are causes of hypergastrinemia. Serum gastrin levels >1000 pg/ml (> 0 times the upper limit of normal) and PH gastric below 2 is the diagnostic of ZES, but two -thirds of ZES patients have serum gastrin levels below 1000 pg/ml. We present the...

ea0032p818 | Paediatric endocrinology | ECE2013

Case report: two patients with Di George syndrome with different diagnostic peculiarities

Coles Diana , Teleanu Raluca , Vasile Daniela , Matei Margarita

Introduction: Di George syndrome is a genetic disorder caused by deletion of chromosome 22. The main features are congenital heart defects, absence or hypoplasia of thymus (with consecutive immunodeficiency and infections), hypoparathyroidism with hypocalcaemia, gastrointestinal problems, delayed psychomotor development, craniofacial abnormalities, tendency to develop seizures and psychiatric disorders.Case report: We present the case of two patients wit...

ea0031p312 | Pituitary | SFEBES2013

Metformin treatment of PCOS: St George's Hospital Endocrine Unit Clinical Experience

Walton Hannah , Mason Helen , Bano Gul

Polycystic ovary syndrome (PCOS) is the most common endocrine condition affecting women and is associated with hyperinsulinaemia and hyperandrogenism. Obesity is present in at least 30% of cases and plays a vital role in the development and maintenance of PCOS as well as affecting the severity of the clinical and endocrine features. Significant improvements in symptoms of androgen excess and ovulatory function are seen with even a modest weight loss of 5% in women with PCOS. M...

ea0011p103 | Clinical case reports | ECE2006

Di-George syndrome presenting with hypocalcaemia and personality disorder in adulthood – a case report

Jose M , Iqbal N , Gaut P , Balakrishnan D , Maksoud H

We report the case of a 42-year-old transsexual with Di-George syndrome (DGS) presenting in adulthood with profound hypocalcaemia and personality disorder. The patient had multiple hospital admissions with episodes of deliberate self-harm and recurrent seizures. Routine investigations revealed hypocalcaemia secondary to hypoparathyroidism. The diagnosis of DGS was delayed until six years later. The clue to the underlying condition was the finding of DGS in the patient’s d...