Publications by authors named "Yao-Han Li"

Article Synopsis
  • About 40% of pheochromocytoma and paraganglioma cases are hereditary and tend to have earlier onset and more complicated symptoms.
  • Specific genetic conditions like von Hippel-Lindau (VHL) and multiple endocrine neoplasia type 2 (MEN2) significantly influence tumor behavior and surgical outcomes, necessitating careful monitoring.
  • A multi-disciplinary team approach is crucial for managing hereditary PPGL cases, as they can involve severe complications in other body systems beyond tumor activity.
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