Searchable abstracts of presentations at key conferences in endocrinology

ea0090p318 | Calcium and Bone | ECE2023

Rare association of primary hyperparathyroidism with type 3 multiple autoimmune syndrome

Aycha Ghachem , Elfekih Hamza , Ghada Sabbagh , Saad Ghada , Fatma Barkallah , Hasni Yosra , Chadli Chaieb Molka

Introduction: Primary hyperparathyroidism (PHPT) is most commonly sporadic and in rare circumstances, it can develop as part of multiple endocrine neoplasia (MEN). There are few cases described in the literature reporting an association of PHPT with myasthenia gravis and multiple autoimmune syndrome (MAS). These patients may present only with clinical signs of PHPT making it difficult to suspect the coexistence of MAS. Here, we report the case of type 3 MAS in a woman with PHP...

ea0090p785 | Thyroid | ECE2023

Thyroid nodular disease in a patient with Neurofibromatosis type 1

Aycha Ghachem , Elfekih Hamza , Ghada Sabbagh , Saad Ghada , Kenza Houd , Hasni Yosra , Chadli Chaieb Molka

Introduction: Neurofibromatosis type 1 (NF1) is a rare autosomal dominant disease. Patients affected by NF1 have an increased risk of developing tumors other than neurofibromas, especially of endocrine origin, that’s why this patients should be screened for endocrine lesions. In this report, we describe a patient affected by NF1 who present a thyroid nodule.Observation: A 27-year-old woman was admitted in our department for endocrinological evaluati...

ea0090ep746 | Pituitary and Neuroendocrinology | ECE2023

Tumor mimicking ampullary carcinoma in a patient with acromegaly

Bnina Molka Ben , Ghada Sabbagh , Elfekih Hamza , Saad Ghada , Fatma Barkallah , Hasni Yosra , Chaieb Molka Chadli

Introduction: Acromegaly is the set of clinical manifestations induced by chronic exposure to an endogenous excess of growth hormone (GH). Most often, acromegaly is related to GH production by a pituitary adenoma. It may be associated with neuroendocrine tumors of the pancreas as part of multiple endocrine neoplasia type 1 (MEN1). Herein, we described a tumor mimicking a carcinoma of the Ampulla of Vater in a patient with acromegaly.Observation: A 54-yea...

ea0090ep627 | Endocrine-related Cancer | ECE2023

A case of synchronous association of stomach neuroendocrine tumor and pernicious anemia

Sabbagh Ghada , Elfekih Hamza , Aycha Ghachem , Saad Ghada , Houd Kenza , Taieb Ach , Ben Abdelkarim Asma , Hasni Yosra , Chadli Chaieb Molka

Introduction: Biermer’s disease is a chronic inflammatory disease due to antibodies targeting parietal cells and intrinsic factor compromising vitamin B12 absorption leading to pernicious anemia, and gastric acid secretion leading to achlorhydria. Neuroendocrine tumors are rare neoplasms that have been reported during the evolution of chronic gastritis. We here describe a case of a type 1 gastric neuroendocrine tumor discovered alongside with Biermer’s disease.<p...

ea0090ep1055 | Thyroid | ECE2023

Transient hypothyroidism post radioiodine therapy

Sabbagh Ghada , Elfekih Hamza , Aycha Ghachem , Saad Ghada , Barkallah Fatma , Taieb Ach , Hasni Yosra , Chadli Chaieb Molka

Introduction: Grave’s disease is an autoimmune disorder and is considered the most common cause of hyperthyroidism. Its treatment options include medical therapy, radioactive iodine (RAI), and surgery. RAI is commonly employed for Grave’s disease regarding its efficiency and safety. Definitive hypothyroidism is the main goal of RAI and is typically achieved within the first 3 to 6 months of therapy. Transient hypothyroidism and recurrence of hyperthyroidism after RAI...