Mutation in Chek2 triggers von Hippel-Lindau hemangioblastoma growth.

Purpose: Von Hippel-Lindau (VHL) is a rare inherited disease mainly characterized by the growth of tumours, predominantly hemangioblastomas (Hbs) in the CNS and retina, and renal carcinomas. The natural history of VHL disease is variable, differing in the age of onset and its penetrance, even among relatives. Unfortunately, sometimes VHL shows more severe than average: the onset starts in adolescence, and surgeries are required almost every year.

Ileal signet-ring cell carcinoma with brain metastases: A case report.

Background: Signet-ring cell carcinoma (SRCC) is a rare subtype of adenocarcinoma that frequently originates in the stomach. Uncommonly, this tumor can lead to brain metastases; an event rarely reported in the literature.

Case Description: A 76-year-old man with a history of cognitive impairment was diagnosed with two brain space-occupying lesions.