Unveiling hepatico-duodenal ligament lymphangioma in a sickle cell disease patient: A radiological and clinical case study.

The 34-year-old female patient with sickle cell anemia had splenomegaly and excruciating stomach discomfort. radiological examinations showed a nonenhancing cystic lesion along the common bile duct, splenic infarcts, and a severely enlarged spleen with subcapsular calcifications, indicative of hepatoduodenal ligament lymphangioma. Minor ascites, borderline hepatomegaly, and a slight left-sided pleural effusion were among the related findings.

A case of spinal cord intramedullary cavernoma.

Rare vascular abnormalities of the central nervous system, spinal intramedullary cavernomas make up fewer than 5% of all spinal cord lesions. Symptoms are vague, making diagnosis difficult. A fast and precise diagnosis is made possible by the early detection and characterization of these lesions, which is made possible by radiological imaging, especially MRI with contrast.

A rare case of gliosarcoma: Comprehensive radiological, histopathological, and clinical insights into diagnosis and management.

Gliosarcoma is a rare and aggressive variant of glioblastoma, characterized by a biphasic histological pattern consisting of both glial and mesenchymal components. This case report describes the clinical presentation, radiological findings, surgical management, and histopathological analysis of gliosarcoma in a 30-year-old female. The patient presented with a 10-day history of right-sided headache and recurrent vomiting.