hrp0089p2-p035 | Adrenals and HPA Axis P2 | ESPE2018

Pseudopubertas Praecox in a 4 Year Old Boy with Bilateral Atypical Adrenocortical Adenomas

Brichta Corinna , Wurm Michael , Hodde Franka , van der Werf-Grohmann Natascha , Schwab Karl Otfried

Introduction: Adrenocortical tumors are very rare in children, with a prevalence of just 0.3 cases/million/year. Autonomic hormone production by adrenal cortical tumors may cause peripheral precocious puberty.Case report: A 4-year-old boy was presented by his parents because of pubertal behavior with aggressive features and a significant increase in the size of the penis. The parents also noticed a strong growth spurt and sweat odor. The boy had a good g...

hrp0098p3-121 | Fetal, Neonatal Endocrinology and Metabolism | ESPE2024

Treatment of an infant with congenital hyperinsulinism due to kcnj11-mutation with octreotide via continuous subcutaneous infusion: a case report

Muehlschlegel Geeske , Alice Manzardo Olimpia , Hodde Franka , Ritter Marie , Van der Werf Natascha , Kamrath Clemens

Background: We present the case of an infant with congenital hyperinsulinism presenting with persisting hypoglycaemias.Case Presentation: The boy was born at 37+3 weeks, weighing 4690g (>99. Percentile, Z-score +3.38). Large for gestational age status was suspected throughout pregnancy, gestational diabetes had been excluded via an oral glucose tolerance test twice. The newborn was initially treated at a secondary car...

hrp0098p3-16 | Adrenals and HPA Axis | ESPE2024

Adrenal insufficiency due to bilateral adrenal haemorrhage in a newborn after suffering perinatal asphyxia: a case report

Alice Manzardo Olimpia , Muehlschlegel Geeske , Hodde Franka , Ritter Marie , Weih Sandra , Van der Werf Natascha , Kamrath Clemens

Background: We describe the case of a male newborn, presenting in our outpatient endocrinological clinic after suffering from a bilateral adrenal haemorrhage in the context of a moderate perinatal asphyxia.Case Presentation: The term male newborn was born spontaneously from breech position after a prolonged labour in a secondary care centre in Freiburg, Germany. Perinatal BGA showed severe metabolic acidosis (pH 6.99, BE...

hrp0098p2-16 | Adrenals and HPA Axis | ESPE2024

The challenge of diagnosis and management of micronodular adrenocortical disease in a 7-year old girl with cyclic cushing syndrome: a case report

Alice Manzardo Olimpia , Ritter Marie , Muehlschlegel Geeske , Hodde Franka , Van der Werf Natascha , Lichte Kai , F Hartmann Michaela , A Wudy Stefan , Kamrath Clemens

Background: We present the case of a 7-year old girl presenting with undulant ACTH independent Cushing syndrome (CS).Case presentation: The patient presented at a secondary care centre with hyperphagia, fatigue and 8 kg weight increase 4 weeks after an upper airway infection. The parents described a similar episode with spontaneous regression 12 months before. At physical examination she showed a cushingoid habitus with ...