ArticleIJU case reports2026
Two Cases of Hereditary Paraganglioma-Pheochromocytoma Syndrome in Siblings, Caused by a Novel Succinate Dehydrogenase Complex Subunit D Variant.
Article in IJU case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
Introduction: Pheochromocytomas and paragangliomas are increasingly recognized as hereditary malignancies, with ~30%-40% of cases involving germline variants. We report a familial case of hereditary pheochromocytoma-paraganglioma syndrome caused by a novel variant in the Case Presentation: An 11-year-old boy was diagnosed with retroperitoneal paraganglioma. Pathological analysis confirmed the resected tumor as a pheochromocytoma and paraganglioma. Conclusion: Early identification of hereditary risks associated with pheochromocytomas and paragangliomas facilitates appropriate lifelong surveillance, timely treatment decisions, and informed genetic counseling.
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