Two Cases of Hereditary Paraganglioma‐Pheochromocytoma Syndrome in Siblings, Caused by a Novel Succinate Dehydrogenase Complex Subunit D Variant

Introduction: gene. Case Presentation: sequencing from blood and tumor tissues revealed a c.74dupT single-nucleotide insertion variant, which was absent from all public databases. Another surgery was performed eight years later because of enlargement of the retroperitoneal mass and elevated plasma norepinephrine levels. His 17-year-old sister was later diagnosed with bilateral adrenal pheochromocytomas. Pathological analysis confirmed the resected tumors as pheochromocytoma and paraganglioma. She harbored the same genetic variant inherited from the children's asymptomatic father. Conclusion: Early identification of hereditary risks associated with pheochromocytomas and paragangliomas facilitates appropriate lifelong surveillance, timely treatment decisions, and informed genetic counseling.