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...

ea0090p246 | Thyroid | ECE2023

Hidden central hypothyroidism in an elderly patient following radioiodine therapy

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

Introduction: Thyrotropin deficiency is a rare etiology of hypothyroidism. The diagnosis can be easily confirmed in case of low FT4 level associated with normal or low TSH value. In patients with peripheral hypothyroidism treated by levothyroxine, this biochemical profile become difficult to find. Herein, we describe the case of a patient with peripheral hypothyroidism due to radioiodine therapy in whom the diagnosis of central hypothyroidism was made.Ob...

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...

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...

ea0073aep561 | Pituitary and Neuroendocrinology | ECE2021

A growth retardation revealing a pituitary stalk interruption syndrome: A case report

Laamouri Rihab , Aycha Ghachem , Rojbi Imen , Besrour Chayma , Lakhoua Youssef , Mchirgui Nadia , Ben Nacef Ibtissem , Khiari Karima

IntroductionPituitary stalk interruption syndrome is an entity radiologically defined by the association of an absent or thin pituitary stalk, an ectopic posterior lobe and a hypoplasia or aplasia anterior lobe. It can manifest as a several of hormonal deficiencies. The circumstances of discovery are multiple. This case illustrates a pituitary stalk interruption syndrome revealed by a growth retardation.Case presentation<p clas...

ea0073ep224 | Thyroid | ECE2021

Acute myocaditis : a rare complication in the Graves disease

Laamouri Rihab , Aycha Ghachem , Rojbi Imen , Besrour Chayma , Lakhoua Youssef , Mchirgui Nadia , Ben Nacef Ibtissem , Khiari Karima

IntroductionGraves’ disease is an autoimmune disorder that has multiple cardiac repercussions including arrhythmias and heart failure. Acute myocarditis is a rarely described complication. In this context, we report a case illustrating this association.Case presentationA 23-year-old man has been followed for Graves’ disease that had been suspected by weight loss, tachycardia and bilateral and asymet...