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 Ewing sarcoma is a very rare tumour with aggressive behaviour and poor prognosis. It tends to metastasize rapidly. Renal extremely rare, only 48 cases have been reported in the literature. Herein, we report case of 14-year-old female presenting painful left flank swelling. Ultrasound magnetic resonance imaging showed large invading kidney, heterogeneously enhanced after injection, associated lymph nodes peritoneal carcinomatosis. A thoraco-abdomino-pelvic computed tomography scan...

Lemmel's syndrome is a rare cause of obstructive jaundice caused by periampullary duodenal diverticulum compressing the intrapancreatic common bile duct with resultant dilatation, patients usually present abdominal pain or jaundice. Cross-sectional imaging beneficial in making diagnosis noninvasively, thus eliminating other pathologies peri-ampullary region. Although rare, we recognize importance considering this to be able make and offer timely treatment. We 2 cases whose retained based on...

Ewing's sarcoma is a primary malignant bone tumor affecting individuals in the second decade of life. Primary sarcomas spine are rare and occurrence very rare. There 2 types spine, sacral which aggressive with poor prognosis non-sacral an extremely occurrence. The patient may have neurological deficit when extends into spinal canal, causing compression cord. Magnetic resonance imaging (MRI) sensitive diagnosing Evaluation extent tumor. Here, we report case 12-year-old boy who presented low...

Ewing's sarcoma is generally an aggressive, poorly differentiated bone and soft tissue tumor affecting children young adults, it accounts for 4%-6% of all primary tumors facial locations occur in only 1%-4% cases, primarily the mandible calvaria. Involvement paranasal sinuses rare. Here we report case 11-year-old girl with no medical, surgical, or traumatic history, who presented 1 month progressive evolution swelling left cheek, associated pain, nasal obstruction, rhinorrhea, a slight...

A real life-threatening emergency, Wunderlich syndrome (WS) is an interesting and unknown clinical condition characterised by intense beginning of spontaneous, non-traumatic renal haemorrhage in the sub-capsular perirenal space, with a typical radiological presentation [1] that allow diagnosis. Although most cases are treated invasively either surgery or embolization to control bleeding, Fortunately our 66 year old patient admitted Mohammed V military hospital Rabat benefited from...

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...

Central neurocytoma is a rare intraventricular tumor, occurring typically in the lateral ventricle of young adults. It considered as neuronal-glial benign tumor with favorable prognosis. Imaging cornerstone allowing accurate preoperative diagnosis on basis several characteristic features. We report case 31-year-old man who has been complaining progressive headaches and whom brain magnetic resonance imaging revealed central neurocytoma. remind then, through literature review, main criteria to...

Tuberculosis of the central nervous system is second most common site after tuberculous meningitis. It represents 0.2% intracranial expansive lesions in some Western countries compared to 10%-30% developing countries. We report case an infant 1 year and 2 months old who presented for 15 days with convulsions asthenia, hypotonia, without fever. The clinical examination laboratory workup were abnormalities. His father had ongoing pulmonary tuberculosis, but no or radiological signs...

Schwannomas are uncommon benign tumors of the peripheral nerves with a low risk malignant transformation. They rarely affect children, can any part body but occur in lower extremity and typically present palpable mass, pain or neurological signs. Imaging helps to orient diagnosis anatomopathological examination confirm it. We report case 12-year-old girl who presented left knee subcutaneous mass overlying tibial tuberosity medially. Clinical revealed positive Tinel's sign. Magnetic resonance...

The first described case of deep dorsal vein thrombosis the penis secondary to vaccine-induced thrombotic thrombocytopenia (VITT), a complication COVID adenoviral vector vaccines. patient reported pain in one month after vaccination. On ultrasound, was found and biological workup ordered confirm VITT trail. Anticoagulant therapy immediately initiated responds well while suffering from erectile dysfunction. is potentially serious event that can be life-threatening; every practitioner should...

Low phospholipid-associated cholelithiasis (LPAC) is a rare, still poorly understood genetic disorder characterized by the association of an ABCB4 mutation and low biliary phospholipid concentration with recurrent cholelithiasis, responsible for development intrahepatic lithiasis in adults. The gene, which codes ABCB4/MDR3 ductal protein, transporter, leads to precipitation cholesterol crystals bile ducts leading formation stones. diagnosis should be suspected when at least 2 following...

Nephroblastoma is a renal blast tumor, the most common malignant tumor in children between 1 and 5 years of age. The average age onset 3.5 years, rarely occurring over 10 Its treatment model medical-surgical collaboration. prognostic factors are mainly stage but recent studies have also shown that advanced child negative factor. We report case 14-year-old who presented with pain swelling right hypochondrium, ultrasound showed heterogeneous retroperitoneal mass, MRI large process origin, T2...

Introduction: It is obvious t interventional radiology (IR) benefits daily from the progress of artificial intelligence requiring training specialized. However, socio-economic differences between North and South seem to be deepened in this direction by lack infrastructures means financing.

Hydatid disease is a zoonosis caused by larva of the tapeworm Echinococcus. All organs can be involved, but it frequently located in liver for adults and lung children. The clinical features are nonspecific. Imaging findings has an important place diagnosis follow-up. Rupture most common complication hydatic cyst variety imaging depending on ruptured layer, amount air within type rupture. We report case 10-year-old boy presenting shortness breath fever among other symptoms revealing chest...

Introduction: Gaucher disease (GD) is a lysosomal storage disorder characterized by the accumulation of glucocerebroside in various cells throughout body. Bone infarction common and fearsome complication. Case Report: We present case 5-year-old child diagnosed with type 3, who exhibited deformation inferior limbs bone pain. Upon evaluation, radiographic examination revealed characteristic triangular appearance metaphysis serpiginous sclerotic area. A magnetic resonance imaging was performed...

Congenital facial palsy is a rare condition that can be categorized into traumatic and developmental etiologies. Trauma related congenital represents by far the most frequent cause with spontaneous complete recovery within weeks, contrary to causes syndromic or non-syndromic, have poor prognosis. We present case of an 11-month-old boy who suffers palsy. He undergoes MRI examination adapted sequences assess nerve, high-resolution CT scan reveals seventh cranial nerve agenesis.

Moyamoya disease (MMD) is an uncommon cerebrovascular disorder characterized by abnormal angiogenesis leading to progressive stenosis of the supraclinoid internal carotid artery. The resultant vascular pathology causes formation a compensatory collateral network, often visualized as characteristic “puff smoke” appearance on imaging. This report aims present case 36-year-old female patient who presented with altered consciousness and left hemiparesis two weeks after undergoing cesarean...

Traumatic dislocation of the testicle is a rare complication that occurs after blunt trauma to scrotum or abdominopelvic injury. The majority cases occur in young adults following severe scrotal motorcycle accident. We report case 1.5-year-old infant admitted for left swelling with inguinal mass. Ultrasound and Doppler examination showed twisted necrotic adenopathy. Surgical exploration emergency room confirmed mass was dislocated an intrascrotal hematoma evacuated followed by orchidopexy testicle.

A malformative syndrome of the lower spine pole, caudal regression is a rare condition (1-5 cases/100 000 births). It usually occurs in children diabetic mothers and includes wide range disorders. This case illustrates subtype this (type IV, group I) non-diabetic mother.