A5035630228- Spinal Dysraphism and Malformations
- Congenital Diaphragmatic Hernia Studies
- Biliary and Gastrointestinal Fistulas
- Renal and Vascular Pathologies
- Fetal and Pediatric Neurological Disorders
- Gastrointestinal disorders and treatments
- Intraperitoneal and Appendiceal Malignancies
- Vascular Malformations Diagnosis and Treatment
- Vascular anomalies and interventions
- Medical History and Research
- Amoebic Infections and Treatments
- Iron Metabolism and Disorders
- Polyomavirus and related diseases
- Pericarditis and Cardiac Tamponade
- Uterine Myomas and Treatments
- Complement system in diseases
- Lung Cancer Treatments and Mutations
- Esophageal and GI Pathology
- Cerebrovascular and Carotid Artery Diseases
- Adrenal and Paraganglionic Tumors
- Infectious Encephalopathies and Encephalitis
- Barrier Structure and Function Studies
- Parvovirus B19 Infection Studies
- Viral-associated cancers and disorders
- Vascular Procedures and Complications
Mohammed V University
2020-2023
Sidi Mohamed Ben Abdellah University
2020-2022
Centre Hospitalier Ibn Sina
2018-2022
Institut National d'Oncologie
2019-2021
Hôpital Militaire Moulay Ismail
2021
Directorate-General Joint Research Centre
2020
Disseminated peritoneal leiomyomatosis (DPL) or peritonealis disseminata is a sporadic benign disease characterized by several solid smooth muscle nodules that proliferate along the abdominopelvic cavity. The source of condition undetermined, although suspected causes include iatrogenic and hormonal stimulation. It primarily affects women reproductive age. Imaging investigations are important in determining extent lesions presence malignancy. There no conventional therapeutic guidelines for...
Lung hernias are rare. They defined by the protrusion of lung parenchyma through a defect in chest wall. A distinction is classically made between supraclavicular, thoracic or diaphragmatic and congenital acquired hernias. The latter can be classified etiology as post-traumatic, postoperative, pathological but spontaneous (even rarer) caused mainly coughing efforts. diagnosis guided clinical presentation confirmed radiographic analysis, especially CT scan. management, conservative surgical...
Lemmel syndrome is a rare and misdiagnosed etiology of obstructive jaundice due to periampullary duodenal diverticulum causing mechanical obstruction the common bile duct. It represents an with absence choledocholithiasis or pancreaticobiliary tumors. underreported entity specific pathognomonic signs.A 77-year-old-woman admitted for sepsis, ascending cholangitis, underwent MRCP gastroduodenoscopy revealing Lemmel's syndrome. Due failure ERCP, patient surgical derivation.Lemmel uncommon...
Neuroglial (glioependymal) cyst is a rare congenital tumor of the central nervous system usually found in childhood. It can be isolated or associated with other brain malformations. Magnetic resonance imaging technique choice for making diagnosis. We report case 10-year-old child who presented epileptic seizures revealing neuroglial and dysgenesis corpus callosum.
Paragangliomas are rare tumors of the neuroendocrine system that form near certain blood vessels (paraaortic and carotid) nerves, often presenting heterogeneous parenchyma displaying strong contrast enhancement on computed tomography. Underdiagnosis misdiagnosis this tumor suspected as they can be silent, small size, or confused with other structures.
Introduction: Delayed presentation of an iatrogenic diaphragmatic injury is rare.We report the case a hernia associated with bowel obstruction occurring as delayed complication right liver resection.This emphasizes rareness such surgical outcome and main CT-scan features rent are discussed along it.Case Report: A 30-year-old female was admitted to our emergency department clinical acute syndrome.A chest abdomen revealed ascent strangulation by entanglement some jejunal loops through hernia.A...
Abstract Pituitary haemochromatosis is an endocrine disorder caused by the accumulation of iron due to a lack absorption during haemochromatosis. The characteristic appearance on MRI T2 and T2* hyposignal anterior pituitary gland without enhancement, respecting stalk posterior gland.