Searchable abstracts of presentations at key conferences in endocrinology

ea0099p391 | Late-Breaking | ECE2024

Surgical outcomes in primary hyperparathyroidism: addressing factors predicting persistent or recurrent hyperparathyroidism

Merhbene Yesmine , Laamouri Rihab , Mekni Sabrine , Essayeh Sawsen , Khiari Karima , Mchirgui Nadia , Rojbi Imen , Ibtissem Bennacef

Background: Primary hyperparathyroidism is a common endocrine disorder characterized by hypercalcemia, resulting from excessive secretion of parathyroid hormone. Parathyroidectomy, is considered as the definitive treatment for this condition, leading in most cases to remission and resolution of hypercalcemia. However, some patients experience surgical failure. Persistent hyperparathyroidism is defined as persistence of hypercalcemia after parathyroidectomy or recurrence of hyp...

ea0099p399 | Late-Breaking | ECE2024

Persistent parathyroid hormone elevation post-parathyroidectomy with biological remission: prevalence and predictive factors

Merhbene Yesmine , Laamouri Rihab , Sawsen Essayeh , Mekni Sabrine , Khiari Karima , Mchirgui Nadia , Rojbi Imen , Ibtissem Bennacef

Background: Primary hyperparathyroidism, is defined by hypercalcemia associated with an elevated or inappropriately normal parathyroid hormone(PTH) levels stemming from hyperfunctioning parathyroid glands. It’s a prevalent endocrine disorder. Parathyroidectomy, the surgical excision of affected glands, stands as the definitive treatment, typically resulting in remission and normalization of calcium levels. However, persistent elevation of serum PTH post-parathyroidectomy ...

ea0099ep86 | Pituitary and Neuroendocrinology | ECE2024

Corticotropic deficiency secondary to wilson disease

Khiari Hager , Mekni Sabrine , Essayeh Sawsen , Rojbi Imen , Ibtissem Bennacef , Lakhoua Youssef , Mchirgui Nadia , Khiari Karima

Introduction: Wilson’s disease is a rare and serious genetic disorder. The accumulation of copper in glands causes several endocrine pathologies. Herein, we report a rare case of hypophysitis with corticotropic deficiency caused by Wilson’s disease.Observation: A 33-years-old female patient was referred to the endocrinology department for hypoglycemia. She had a history of Wilson’s disease diagnosed at the age of nine complicated by cirrho...

ea0099ep448 | Reproductive and Developmental Endocrinology | ECE2024

Clinical and biological aspects of isolated hypogonadotropic hypogonadism

Khiari Hager , Rojbi Imen , Essayeh Sawsen , Mekni Sabrine , Ibtissem Bennacef , Lakhoua Youssef , Mchirgui Nadia , Khiari Karima

Introduction: Isolated hypogonadotropic hypogonadism is a heterogeneous group of genetic abnormalities affecting the hypothalamic pituitary gonadal axis. The main mechanism consists of an impairment of the production or the action of gonadotropin releasing hormone (GnRH). While several mutations have been identified, the majority of cases remain without etiology. The objective of our study was to describe the clinical and biological profiles of these diseases.<p class="abs...

ea0099ep682 | Thyroid | ECE2024

The onset of thyroid eye disease in hyperthyroidism after covid-19 infection: a case report

Khiari Hager , Mekni Sabrine , Essayeh Sawsen , Rojbi Imen , Ibtissem Bennacef , Lakhoua Youssef , Mchirgui Nadia , Khiari Karima

Introduction: Thyroid eye disease (TED) is an autoimmune inflammatory disorder affecting the orbital tissues. It occurs with thyroid dysfunction notably Graves’ disease. TED exhibits different severity patterns and has a lot of risk factors. We, herein, report a rare case of a severe TED developing after COVID-19 infection in a patient initially treated for hyperthyroidism without ocular manifestations.Observation: A 48-year-old female with a histor...