ABSTRACT
Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder found in children as well as adults. It is characterized by hemi cerebral atrophy. To date, very few cases of this disorder have been reported. Radiological imaging including magnetic resonance imaging (MRI) and computed tomography (CT) are accurate tools for the diagnosis of DDMS. We present a case of a 13-year-old female child who came with complaints of multiple episodes of generalized tonic-clonic seizures. In our case, clinical history and imaging with CT and MRI were accurate enough to diagnose DDMS.
ABSTRACT
We report a case of a solid pseudopapillary epithelial neoplasm of the pancreas in a 19-year-old female who presented with abdominal pain. Computed tomography of the abdomen showed a heterogenous density mass in the tail of the pancreas. The mass had fluid density in the central region and soft tissue density in the peripheral region. Post-contrast evaluation showed enhancement in the peripheral solid component. Based on the radiological investigation carried out at our institute, a diagnosis of solid pseudopapillary epithelial neoplasm of the pancreas was established which was confirmed on histopathology.
