Fig. 1From: Identification of a VHL gene mutation in atypical Von Hippel-Lindau syndrome: genotype–phenotype correlation and gene therapy perspectiveSchematic program of the medical history, diagnosis and treatment workflow of patient in whole process. Specially, the patient underwent two operations aiming to pheochromocytoma and paraganglioma (PPGLs), followed by findings of lung and pancreas neuroendocrine tumor NET and subjected to octreotide-based radionuclide therapyBack to article page