Searchable abstracts of presentations at key conferences in endocrinology

ea0067gp12 | Poster Presentations | EYES2019

Long term evolution of a patient with metastatic neuroendocrine carcinoma of unknown primary site: A clinical puzzle for the endocrinologist

Mitru Natalia , Galoiu Simona , Poiana Catalina

Background: Carcinoid tumors are rare and slow growing malignancies derived from enterochromaffin cells. Two-thirds of carcinoid tumors arise in the gastrointestinal tract, and in 3% of these cases the primary site cannot be determined. Presenting symptoms depend on the location of the primary tumor may be nonspecific and in 13% of patients distant metastases are discovered on diagnosis.Case presentation: A 64 years old woman was admitted for diffuse abd...

ea0090p390 | Endocrine-related Cancer | ECE2023

Efficacity of combination of Lenvatinib and PPRT in severe hypersecretion of VIP

Raluca Mitru Natalia , Hadoux Julien , Lamartina Livia , Pani Fabiana , Baudin Eric , Moog Sophie

Introduction: VIPomas are rare neuroendocrine tumors (NET), usually located in the pancreas that secrete vasoactive intestinal polypeptide (VIP) leading to high-volume watery diarrhea and complications such as hypokalemia, acidosis and dehydration. The management of VIPoma symptoms is often challenging when surgical resection of all the lesions is not feasible. Treatments are then based on somatostatin analogs (SSA) and may also include hepatic chemoembolization, systemic chem...

ea0073aep429 | General Endocrinology | ECE2021

Case report: The spectrum of autoimmune thyroid disease in association with chromosome 18p deletion syndrome

Vasilescu Sorana , Mitru Natalia Raluca , Massarella Alberto , Andrei Anca , Preda Diana , Mirica Alexandra

IntroductionChromosome 18p deletion syndrome is a rare chromosomal abnormality caused by the complete or partial delation of the short arm of chromosome 18, represented by facial dysmorphic features, hypodontia, microcephaly, short webbed neck, intellectual disability, reproductive system dysplasia, rarely with autoimmune disorders and IgA, IgG or IgM deficiency. A small subset of patients, approximately 9–10% have cardiac/brain disorders. Circa 150...

ea0073ep32 | Calcium and Bone | ECE2021

Secondary hyperparathyroidism associated with exostosis in a 10-year-old girl: a case report

Maria Andrei Anca , Mitru Natalia , Vasilescu Sorana , Preda Diana , Mirica Alexandra

BackgroundSecondary hyperparathyroidism is a condition that can occur as a result of low vitamin D level. Parathyroid hormone (PTH) has the role of stimulating bone resorption by two mechanisms: direct activation of osteoblasts and indirect stimulation of osteoclast. Exostosis or bone spur is a benign tumor that consists in overgrowth of a pre-existing bone. Exostoses can affect any bone, however they are most commonly located on the bones of the joints ...

ea0073ep179 | Reproductive and Developmental Endocrinology | ECE2021

A difficult diagnosis: menstruation-related periodic hypersomnia

Raluca Mitru Natalia , Vasilescu Sorana , Andrei Anca , Preda Diana , Alexandra Mirică

IntroductionKleine-Levin syndrome, also called recurrent hypersomnia is a rare sleep disorder characterized by recurrent episodes of severe hypersomnia associated with cognitive and behavioral disturbances such as confusion, derealization, apathy, compulsive eating and hypersexuality. Menstrual-related hypersomnia is classified as a subtype of syndrome Levin-Kleine consisting of recurrent hypersomnia that is temporally linked with menses.<p class="ab...