Searchable abstracts of presentations at key conferences in endocrinology

ea0041s7.3 | The chronic syndromes of patients with cured pituitary diseases (<emphasis role="italic">Endorsed by the European Journal of Endocrinology</emphasis>) | ECE2016

Craniopharyngioma: 10 years after cure

Muller Hermann L

Childhood-onset craniopharyngiomas are rare intracranial embryonal malformations of the sellar region arising from remnants of Rathke’s pouch that require life-long control and management of the endocrine, ophthalmological and neuropsychological deficits caused by the tumors and their treatment. Craniopharyngiomas show low-grade histological malignancy and frequently affect hypothalamic/pituitary regions and the optic chiasm due to their location. Hypothalamic involvement...

ea0041ep249 | Clinical case reports - Pituitary/Adrenal | ECE2016

Spinal metastasis in childhood-onset craniopharyngioma: Case report, review of the literature and experiences in the German childhood-onset craniopharyngioma registry

Jaspers Martin , Hoffmann Anika , Lohle Kristin , Brentrup Angela , Muller Hermann L

Background: Remote recurrence and metastasis are unusual complications in childhood-onset adamantinomatous craniopharyngioma mainly occurring either along a previous surgical route or by seeding via cerebrospinal fluid.Case description: An 11-year-old female patient initially presented with headache and neck pain as well as nausea over the course of 2 months. A sellar/suprasellar mass (4.0 cm×4.0 cm 5.0 cm) was detected on magnetic resonance imaging...

ea0041ep740 | Neuroendocrinology | ECE2016

Nonalcoholic fatty liver disease and fatigue in long-term survivors of childhood-onset craniopharyngioma

Hoffmann Anika , Bootsveld Klaus , Gebhardt Ursel , Daubenbuchel Anna M. , Sterkenburg Anthe S. , Muller Hermann L.

Objective: Hypothalamic obesity in childhood craniopharyngioma (CP) patients bares a high risk for development of metabolic syndrome. In metabolic syndrome, the development of nonalcoholic fatty liver disease (NAFLD) is known. The aim of this study is to detect the risk for NAFLD in childhood-onset CP.Design: This cross-sectional study included liver computed tomography (CT); ultrasound analysis of abdomen; measurements of serum parameters, height, weigh...

ea0041ep766 | Neuroendocrinology | ECE2016

Hydrocephalus and hypothalamic involvement in pediatric patients with craniopharyngioma or cysts of Rathke’s pouch: impact on long-term prognosis

Daubenbuchel Anna M , Hoffmann Anika , Gebhardt Ursel , Warmuth-Metz Monika , Sterkenburg Anthe S , Muller Hermann L

Objective: Pediatric patients with sellar masses such as craniopharyngioma (CP) or cyst of Rathke’s pouch (CRP) frequently suffer disease- and treatment-related sequelae. We analyzed the impact and prognostic relevance of initial hydrocephalus (HY) and hypothalamic involvement (HI) on long-term survival and functional capacity (FC) in children with CP or CRP.Subjects and methods: Using retrospective analysis of patient records, presence of initial H...

ea0041ep739 | Neuroendocrinology | ECE2016

Nuchal Skinfold Thickness: a novel parameter for assessment of body composition in childhood craniopharyngioma

Sterkenburg Anthe S. , Hoffmann Anika , Reichel Julia , Lohle Kristin , Eveslage Maria , Warmuth-Metz Monika , Muller Hermann L.

Context: Hypothalamic obesity, subsequent cardiovascular disease (CVD), and relapses/progression have major impact on prognosis in childhood-onset craniopharyngioma (CP). We analyzed nuchal skinfold thickness (NST) on magnetic resonance imaging (MRI) performed for follow-up monitoring as a novel parameter for body composition (BC) and CVD in CP.Objective: Identify association of NST with body mass index (BMI), waist-to-height ratio (WHtR), caliper-assess...

ea0041ep765 | Neuroendocrinology | ECE2016

History before diagnosis in childhood craniopharyngioma: associations with initial presentation and long-term prognosis

Hoffmann Anika , Boekhoff Svenja , Gebhardt Ursel , Sterkenburg Anthe S , Daubenbuchel Anna M , Eveslage Maria , Muller Hermann L

Objective: Childhood craniopharyngiomas (CP) are often diagnosed after long duration of history (DOH). Tumor size, hypothalamic involvement (HI), and obesity are associated with reduced overall survival (OS) and functional capacity (FC). The effect of DOH and specific symptoms in history on presentation at initial diagnosis and long-term prognosis are unknown.Design: Retrospective analysis of patients’ records and prospective longitudinal follow-up....