A5110989463- Congenital Anomalies and Fetal Surgery
- Parasitic infections in humans and animals
- Gastrointestinal disorders and treatments
- Amoebic Infections and Treatments
- Vascular anomalies and interventions
- Sarcoma Diagnosis and Treatment
- Urologic and reproductive health conditions
- Bone Tumor Diagnosis and Treatments
- Vascular Malformations and Hemangiomas
- Gastrointestinal Tumor Research and Treatment
- Endometriosis Research and Treatment
- COVID-19 diagnosis using AI
- Liver Disease and Transplantation
- Infectious Diseases and Tuberculosis
- Medical Imaging and Pathology Studies
- Adrenal and Paraganglionic Tumors
- Urinary and Genital Oncology Studies
- IgG4-Related and Inflammatory Diseases
- Intracerebral and Subarachnoid Hemorrhage Research
- Neurofibromatosis and Schwannoma Cases
- Abdominal vascular conditions and treatments
- Cerebrospinal fluid and hydrocephalus
- Intraperitoneal and Appendiceal Malignancies
- Congenital Diaphragmatic Hernia Studies
- Appendicitis Diagnosis and Management
Centre Hospitalier Ibn Sina
2016-2025
Ibn Sina Hospital
2021-2025
Mohammed V University
2015-2025
University Radiology
2023
Assistance Publique – Hôpitaux de Paris
2007
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...
Abstract Accessory spleens are a congenital anomaly caused by abnormal fusion during embryonic development, leading to the presence of splenic tissue in unusual locations, such as tail pancreas. Their pronounced arterial enhancement can cause them be mistaken for neuroendocrine tumor, particularly an insulinoma. We report case 61-year-old patient with recurrent hypoglycemia who was referred suspected tumor.
Cannabis use is increasing rapidly among young people worldwide despite the deleterious effects of this toxic substance on health. We report a case acute hippocampal encephalopathy in heavy cannabis user (8-10 joints/d for 6 years) who presented with nonfebrile status epilepticus. Brain magnetic resonance imaging revealed bilateral and symmetrical high-signal abnormalities regions. The damage to these regions often severe, long-lasting, sometimes irreversible. Therefore, every doctor...
Persistent left superior vena cava (PLSVC) is a rare anomaly of the systemic venous circulation. We report case 22-year-old female that had history multiple repair surgeries for her esophageal atresia, as well right lobectomy bronchiectasis 15 years prior. She was admitted to surgical ward complete resection lung. A trans-thoracic echocardiography performed part pre-surgical work-up and it revealed dilated coronary sinus which led us suspect presence PLSVC. The latter confirmed by simple...
Idiopathic tumoral calcinosis is a very uncommon benign disease, defined by the presence of calcified deposits in periarticular tissues. The pathogenesis yet not well understood. treatment remains essentially surgical and prognosis good. We report case 50-year-old patient presenting with firm mass soft tissues limitation motion his right hip joint. diagnosis was first hand suggested radiologically due to voluminous calcifications no bone involvement, later on confirmed pathology results....
Cystitis glandularis is a rare benign condition, occurring in only 1% of the general population, and it tends to affect males more frequently. This pathology characterized by reactive metaplasia bladder's urothelium, which results from chronic recurrent irritation bladder wall. Symptoms are nonspecific primarily marked an irritative urinary syndrome accompanied hematuria. We present case young male patient with cystitis glandularis, discovered as result bilateral uretero-hydronephrosis...
Considered rare, the synovitis-acne-pustulosis-hyperostosis-osteitis (SAPHO) syndrome is a distinct clinical entity, associating skin manifestations and osteoarticular symptoms. Anterior chest wall pain centered at sternoclavicular sternocostal joints an important characteristic finding that can lead to its diagnosis. Radiologists clinicians must be aware of as it mimic some more common disease entities such Paget's disease. We report case 63-year-old male patient, with no significant...
Primary hepatic lymphoma is rare. Clinical and radiological presentations are not specific. The diagnosis often late. Chronic hepatitis or cirrhosis, especially post-viral C usually precedes primary liver lymphoma. differential arises mainly with other tumors, such as atypical hypovascular cellular hepatocellular carcinoma when there cirrhosis metastases, colorectal, stomach lung metastases. Other tuberculosis sarcoidosis, particularly multiple lesions. We report the case of a 52-year woman,...
Lemmel’s syndrome is a rare and misdiagnosed cause of obstructive jaundice. The the obstacle duodenal diverticulum located at periampullary generating compression effect on common bile duct with secondary dilation extra- intra-hepatic ducts. Late diagnosis this entity may lead to unnecessary further investigations therapeutic delay. There are only few case reports condition. We report 77-year-old female presenting jaundice due syndrome. was made set clinical, biological radiological...
Urachal anomalies are infrequent in the adult population and may represent a diagnostic challenge. Few cases of urachal sinuses reported usually asymptomatic unless complication occurs, most likely infectious. Infected sinus' clinical manifestations purulent umbilical discharge, abdominal pain, periumbilical mass. We report case late presentation an infected sinus male adult. Clinical imaging features allowed accurate diagnosis. Antibiotic therapy was followed by remnant’s surgical excision....
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...
Mucosal melanoma is a rare subtype of distinct from the cutaneous type in its clinical and biological aspects, requiring different therapeutical management. Anorectal melanomas represent less than 1% anorectal cancers 0.3% malignant melanomas, they are by far most studied type. Proctologic examination, colonoscopy, biopsy can establish correct diagnosis. Imaging techniques, especially MRI show some characteristic features, but it essentially performed for extension assessment. We report case...
Kienböck disease is a condition characterized by avascular necrosis of the lunate bone. Advanced imaging can aid in diagnosis and staging disease. Magnetic resonance (MRI) an important adjunct to diagnosis. In particular, MRI helpful early when plain radiographs may not reveal abnormalities. A 17 -year-old man with who underwent radiography MR described this article.
Abstract Key prognostic elements to consider in sarcoidosis patients who contract COVID‐19 pneumonia are pulmonary involvement, the underlying immune system dysfunction, immunosuppressive therapies’ use, and increased risk for hypercoagulability.
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.
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.