Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep622 | Endocrine-Related Cancer | ECE2022

Refractory papillary thyroid carcinoma treated with sorafenib: an Algerian experience

Bouchenna Amira , Tibouk Abdelghani , Brahim Ghennam , Samia Ould Kablia

Introduction: 5-10% of papillary thyroid carcinoma develop metastatic disease, of which about 60-70% will become refractory to radioactive iodine. Significant negative impact on the prognosis and an average life expectancy of 3 to 5 years.Material and method: Since 2018, patients with refractory thyroid carcinoma and considered to be progressive according to the RECIST criteria have been treated with anti tyrosine Kinase type sorafenib.<p class="abst...

ea0081ep940 | Reproductive and Developmental Endocrinology | ECE2022

Disorders of sex development 46XY revealed at adult age : A report of three cases and and literature review

Katia Benabdelatif , Iabbassen Malek , Meriem Bensalah , Samia Ould Kablia

Introduction: Disorders of sex development include a large number of congenital conditions related to unusual chromosomal sex (gonosomal abnormalities), defective testicular development, or abnormal hormone secretion or receptivity, resulting in unusual external and/or internal genitalia development rare. Patients and methods we report 3 cases of disorders of sex development 46XY reveled at adult age. clinical, biological and radiological funding are reported in the following ...

ea0081ep1146 | Thyroid | ECE2022

Papillary carcinoma of the thyroid associated with Marine-Lenarth syndrome: about a case

Bouchenna Amira , Tibouk Abdelghani , Brahim Ghennam , Samia Ould Kablia

Introduction: The Marine-Lenhart syndrome (MLS) is commonly defined as a combination of Graves’ disease and autonomous functioning thyroid nodule (s). the risk of malignancy of these nodules is less than 1% We report a case.Observation: 27-year-old patient, hospitalized for treatment of a basal disease, cervical ultrasound found a 1.5 cm lower left lobe thyroid nodule classified eutirads 4. the sintigraphy found an aspect of diffuse hypercaptive goi...

ea0063p351 | Thyroid 1 | ECE2019

Anaplastic thyroid carcinoma or radiation-induced sarcoma: About a case

Amira Bouchenna , Abdelghani Tibouk , Youcef Bakkouche , Samia Ould Kablia

Introduction: Anaplastic thyroid cancer has long been considered as a mesenchymal tumor (sarcoma). To date, it is difficult to differentiate between the two types. Radio-induced sarcomas of the head and neck are a very rare entity. Their annual incidence is 0.06 to 0.17%.Observation: We report the case of a 83-year-old patient, with a history of breast neoplasia treated with radiotherapy 7 years ago. Followed for a year for papillary carcinoma of the thy...

ea0020p321 | Clinical case reports and clinical reports | ECE2009

A primary differentiated carcinoma of ectopic mediastinal thyroid: report of two cases

Yamina Aribi , Samia Ould Kablia , Rosa Akrouf , Zahra Kemali

Thyroglossal ductal cyst is the most common congenital cervical pathology. Abnormalities in the embryologic development and migration of the thyroid gland can result in this ectopic thyroid tissue, which may occur in the midline in any position from the base of the tongue to the mediastinum. They are rarely seen in adults. Malignant transformation of the cyst is quite rare and is encountered mostly in adults.We retrospectively reviewed two cases of thyro...

ea0020p619 | Reproduction | ECE2009

Clinical characteristics of Algerian PCOS women

Samia Ould-Kablia , Yamina Aribi , Zahra Kemali , Mourad Semrouni

Polycystic ovary syndrome (PCOS) is the most frequent endocrinopathy in premenopausal women, and has many clinical features in common with the metabolic syndrome.Objective: The aim of our study was to evaluate the clinical characteristics of our PCOS women.Methods: Of 181 PCOS defined by the Rotterdam criteria and 90 controls were evaluated for anthropometric parameters by physical examination.Results: The PC...

ea0081ep20 | Adrenal and Cardiovascular Endocrinology | ECE2022

Adrenal hemangioma with subclinical cushing’s syndrome

Samia Ould Kablia , Benfiala Mouna , Katia Benabdelatif , Kassa Reda , Bouchenna Amira

Introduction: Adrenal cavernous hemangioma is a rare tumor with few cases reported in the world. Usually this adrenal masses are incidentally discovered and non functional.Case report: We describe the case of a 63 year old male patient with a history of hypertension and treated prostate. He was referred to our endocrinology department with complaints of his left lower back. At the admission the BMI was 21 kg/m2, his blood pressure was 160/90 m...

ea0081ep99 | Adrenal and Cardiovascular Endocrinology | ECE2022

Geant myolipoma adrenal: report of two cases and literature review

Katia Benabdelatif , Benfiala Mouna , Meriem Bensalah , Aicha Lachkhem , Samia Ould Kablia

Introduction: Adrenal myelolipoma is a rare, benign and nonfunctional tumor composed of mature adipose and hematopoietic cells. It is often of incidental finding (8%) and the diagnosis is based on radiological imaging. We report two cases of giant adrenal myelolipoma and discuss the diagnostic and therapeutic aspects of this pathology.Observation: Patient D.K 40 years old, hospitalized for adrenal mass revealed by right back pain radiating to the right h...

ea0063ep149 | Thyroid | ECE2019

Primary thyroid lymphoma: about two cases

Amira Bouchenna , Badreddine Kharkhache , lila Brakni , Nadjet Ould Kablia , Abdelghani Tibouk , Khadidja Djouadi , Samia Ould Kablia

Introduction: Primary thyroid lymphomas are rare (2–5% of thyroid cancers and less than 5% of extra-ganglionic lymphomas). The most frequent types are B-cell lymphoma and MALT lymphoma. Posing a diagnosis problem, including differential diagnosis with anaplastic cancer. We report two different cases of thyroid lymphoma.Observation: Case 1: Women 64-year-old, followed by 7 years for Hashimoto’s thyroid consulted for a cervical mass, of rapid evo...

ea0049ep120 | Clinical case reports - Pituitary/Adrenal | ECE2017

Hemangioma a rare adrenal tumors: report of two cases

Yamina Aribi , Meriem Bensaleh , Lila Brakni , Malek Iabassen , Samia Ould Kablia

Introduction: Dramatically with increased use of computed tomography (CT) and magnetic resonance imaging (MRI), more and more uncommon adrenal masses have been detected at abdominal examinations. Adrenal cavernous hemangiomas (ACH) are rare vascular tumor. The first case report was published in 195 by Johnson and Jeppesen. Approximately less than 70 cases were reported in the literature to date.ACH are nonfunctioning benign tumors that is often discovere...