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...

ea0099ep1041 | Thyroid | ECE2024

Subclinical hyperthyroidism: exploring etiologies, clinical profiles and outcomes

Myriam Baltagi , Essayeh Sawsen , Rojbi Imen , Ben Nacef Ibtissem , Mekni Sabrine , Laamouri Rihab , Khiari Karima

Introduction: Subclinical hyperthyroidism (SH) is defined by normal thyroid hormone levels and reduced thyroid-stimulating hormone (TSH) concentration. It still raises intriguing questions about its clinical impact, management and outcomes. The aim of our study was to determine the underlying etiologies of SH, its clinical features and its outcomes in Tunisian patients.Methods: We conducted a retrospective study at Charles Nicolle Hospital, including 46 ...

ea0081ep220 | Calcium and Bone | ECE2022

Endocrine disorders and osteoporosis: case series

Adel Meriem , Mekni Sabrine , Jridi Maysam , Rojbi Imen , Lakhoua Youssef , Mchirgui Nadia , Nacef Ibtissem Ben , Khiari Karima

Introduction: Homeostasis of calcium and phosphor influence bone metabolism. They depend on several hormones, including parathyroid hormone, thyroid and sexual hormones. Low bone mass seems a common issue in endocrine disorders. The aim of this study is to identify the different endocrine disorders in patients with low bone mass.Methods: Retrospective study collecting the medical files of patients followed in the endocrinology department of Charles Nicol...

ea0081ep301 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Endogenous hyperinsulinism and diabetes remission : A report of 2 cases

Ben Rebai Senda , Ben Nacef Ibtissem , Mekni Sabrine , Besrour Chayma , Lakhoua Youssef , Mchirgui Nadia , Rojbi Imen , Khiari Karima

Introduction: Diabetes is a chronic, progressive disease characterized by elevated levels of blood glucose. In type 1 diabetes, some patients experience a “honeymoon period” shortly after diagnosis, wherein insulin needs decrease significantly and a few studies have demonstrated that drug-free glycemic control can be achieved in type 2 diabetes. We describe 2 unusual cases of endogenous hyperinsulinism and diabetes remission.Case presentation 1...

ea0081ep603 | Endocrine-Related Cancer | ECE2022

Multiple endocrine neoplasia type 1: A case report

Adel Meriem , Nacef Ibtissem Ben , Besrour Chayma , Mekni Sabrine , Smadhi Houaida , Lakhoua Youssef , Mchirgui Nadia , Rojbi Imen , Khiari Karima

Introduction: Multiple endocrine neoplasia (MEN1) is a rare underdiagnosed inherited multi-tumor syndrome, affecting neuroendocrine and non-endocrine tissues. Its aspects are extremely variable with no genotype-phenotype correlation.Case report: A 57 year old woman with a history of hypertension, presented five months before her admission with asthenia, headache and vomiting, initial biological exams revealed a central hypothyroidism. A pituitary MRI sho...

ea0081ep812 | Pituitary and Neuroendocrinology | ECE2022

Hypopituitarism induced Radiotherapy for nasopharyngeal carcinoma: a case report

Adel Meriem , Nacef Ibtissem Ben , Kamoun Elyes , Mekni Sabrine , Lakhoua Youssef , Mchirgui Nadia , Rojbi Imen , Khiari Karima

Introduction: Since the hypothalamic-puituitary axis (HPA) is a radiosensitive region, cranial radiotherapy for head and neck malignancies represents a major risk factor for the development of endocrine complications particularly hypopituitarism.Case report: A 22 years old girl with a history of a undifferentiated carcinoma of nasopharyngeal type UCNT at the age of 09 years old treated with radiotherapy and chemotherapy was referred to the endocrinology ...