Pituitary apoplexy within a prolactin-secreting macroadenoma in a child: A rare clinical entity with radiological correlation.

Pituitary apoplexy is an uncommon but potentially fatal syndrome of the pituitary gland, caused by ischemia, hemorrhage, or necrosis that can occur with or without a pre-existing pituitary neuroendocrine tumor (PitNET), as reported during pregnancy and in lymphocytic hypophysitis. We present in this paper a case of an 11-year-old girl with pituitary apoplexy. Our patient experienced sudden deterioration in her left eye vision and a headache.

An unusual cause of ileal volvulus, a giant mesenteric cystic lymphangioma.

Volvulus of the midgut involves twisting of the small bowel around its mesenteric axis. It is frequently associated with malrotation in children, it can also be attributed to other causes such as tumors. Mesenteric lymphangiomas account for only 5% of all lymphangiomas, and small bowel lymphangiomas represent less than 1% of all cases.

Wandering spleen torsion with splenic vein thrombosis: A case report.

Wandering spleen is a rare condition characterized by the absence or underdevelopment of one or all of the ligaments that hold the spleen in its normal position in the left upper quadrant of the abdomen. It is an uncommon clinical entity that mainly affects children. Among adults, it most frequently affects women of reproductive age, in whom acquired laxity of the splenic ligaments is usually the cause.

Intussusception caused by cecal duplication cyst mimicking appendicitis: A case report.

The cecum is an uncommon location for intestinal duplication cysts. They are usually identified within the first 2 years of a child's life. Symptoms can vary, but often include nausea, stomach pain, bloating, a noticeable lump, and rectal bleeding.

Beyond the expected: MRI features of a primary retro-uterine neuroendocrine tumor: A case report.

Primary pelvic neuroendocrine tumors (NETs) are exceptionally rare, especially in older women, and present considerable diagnostic challenges due to their nonspecific clinical presentation and their unhabitual pelvic retroperitoneal location. In this case report, we highlight an uncommon case of a neuroendocrine tumor (NET) in an elderly female, emphasizing the crucial role of imaging modalities in diagnosis and management. The patient presented with vague abdominal discomfort, Motivating a detailed imaging investigation.