A5016701845- Vascular Malformations Diagnosis and Treatment
- Management of metastatic bone disease
- Cancer Diagnosis and Treatment
- Endometriosis Research and Treatment
- Vascular Anomalies and Treatments
- Traumatic Ocular and Foreign Body Injuries
- Neuroblastoma Research and Treatments
- Ocular Disorders and Treatments
- Ocular Oncology and Treatments
- Intraperitoneal and Appendiceal Malignancies
- Case Reports on Hematomas
- Gynecological conditions and treatments
- Pectus Deformity Diagnosis and Treatment
- Meningioma and schwannoma management
- Abdominal vascular conditions and treatments
- Adrenal and Paraganglionic Tumors
- Infective Endocarditis Diagnosis and Management
- Renal and related cancers
- Aortic Disease and Treatment Approaches
- Intraocular Surgery and Lenses
- Pelvic floor disorders treatments
- Multiple Sclerosis Research Studies
- Uterine Myomas and Treatments
- Pediatric Urology and Nephrology Studies
- Hormonal Regulation and Hypertension
Mohammed V University
2023-2025
Military Hospital
2025
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 A 70-year-old patient with a history of skull base osteomyelitis experienced slurred speech, dizziness, and coordination issues. He had been treated both intravenous oral metronidazole. Brain MRI revealed symmetrical areas hyperintensity in the bilateral dentate nuclei, tectum, splenium corpus callosum. These abnormalities nearly completely disappeared few days after stopping medication. Metronidazole, frequently used as an antiparasitic antibacterial drug, can lead to...
Abdominal pain is a common occurrence in the adolescent demographic, encompassing wide range of differential diagnoses. The etiology abdominal can be categorized into gastrointestinal, urologic, and gynecologic causes. In female pediatric population, acute urinary retention an uncommon but noteworthy source pain, typically resulting from obstructive process. Hence, it imperative to perform comprehensive physical examination prior deciding on management approach. We present case 11-year-old...
Spinal cord cavernous malformation is a rare and uncommon vascular malformation, it may remain asymptomatic for long period or manifest as sudden gradual change in spinal functioning. The diagnosis relies essentially on magnetic resonance imaging (MRI). Surgery constitutes the majority of management with all complications that can occur during after surgery. We report case intramedullary cavernoma 12-year-old patient admitted acute paraparesia bowel bladder dysfunction. MRI revealed 2...
Nephrogenic rests (NRs) are foci of embryonic nephrogenic cells that persist beyond the 36th week gestation. They precursor lesions Wilms tumor and found incidentally in approximately 1% infants. The term nephroblastomatosis (NBS) is utilized when extensively or multifocally affect kidneys. We report a case left nephroblastoma with bilateral nephroblastomatosis, treated neoadjuvant chemotherapy followed by nephrectomy, highlighting imaging features on ultrasound, CT, MRI, potential...
Neuroblastomas commonly metastasize to the cranium and orbit, although other facial bones were less implicated. In this report we present a 3 years old child with metastatic neuroblastoma mandible that presented swollen right jaw. The first assessment of head computed tomography revealed soft tissue mass permeative lytic changes osseous structures centered on mandible, as well osteo-meningitis metastases. These masses proven be lesions from intra-abdominal adrenal gland. Over previous...
Acute disseminated encephalomyelitis (ADEM) is an acute and rapidly progressive auto-immune demyelinating disorder in the central nervous system. It a rare disease but more frequently observed pediatric population. We report case of monophasic postvaccination ADEM, which presented with paraparesis associated fever. showed favorable evolution under corticosteroids, without recurrence after 3 years follow-up. The diagnosis was established due to context MRI abnormalities characteristics. This...
Adrenal gland cysts are rare and uncommon manifestations. Mostly asymptomatic, discovered incidentally during radiological studies or at autopsy, without characteristic symptoms. The spectrum of these entities may include benign malignant cystic neoplasms. They classified into four types: pseudocysts, endothelial cysts, epithelial parasitic cysts. Though pseudocysts reported to be the most frequently clinically recognized adrenal in surgical series, more frequent autopsy series. Even with...
Epiploic appendagitis is a benign and self-limiting condition that has garnered more recognition, particularly in preoperative settings, thanks to advancements imaging techniques, notably computed tomography (CT). Its distinct radiologic features facilitate accurate diagnosis prior surgery. Despite its unique characteristics, the clinical presentation of epiploic often resembles various other intra-abdominal medical surgical conditions, leading potential confusion. Here, we present case...
Optic nerve coloboma is a congenital defect caused by the incomplete closure of embryonic fissure. This begins around fifth week gestation, when embryo measures approximately 7 to 14 mm. Colobomas may appear as isolated defects or alongside other ocular and systemic abnormalities. They typically occur in inferonasal quadrant, where optic vesicle undergoes closure. process starts centrally within eye progresses both anteriorly posteriorly. The distinct nature these closures can result an...
Neurofibromatosis type 2 (phacomatosis) is a rare inherited autosomal dominant condition defined by the development of numerous central neuronal tumors. In addition to classic intracranial schwannomas, and spinal meningiomas, intramedullary ependymomas, it can be associated with few cutaneous abnormalities. this report, we discuss case 21-year-old female who was examined for persistent headache masses bilateral hearing loss. Magnetic resonance imaging cranium whole spine detected multiple...