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Among these, only a limited subset includes tumors with distinctive oncocytic features, highlights the necessity for pathologists and clinicians to pursue further investigation in affected patients and their families. Summary: Advances in genetic research and diagnostic pathology have highlighted the germline predispositions underlying these tumors, which manifest across multiple organ systems, including thyroid, parathyroid, renal, and adrenal glands. This review examines the clinical, pathological, and molecular features of oncocytic neoplasms in the context of hereditary syndromes such as Carney complex, Li-Fraumeni syndrome, DICER1 syndrome, Birt-Hogg-Dub\u00e9 syndrome, hyperparathyroidism-jaw tumor syndrome, hereditary leiomyomatosis and renal cell carcinoma syndrome, tuberous sclerosis syndrome, Beckwith-Wiedemann syndrome, and SDH-deficient hereditary paraganglioma\/pheochromocytoma syndrome. It emphasizes the importance of recognizing syndromic associations through histopathological clues, genetic testing, and family history to facilitate accurate diagnosis and tailored management. Key Message: By integrating clinical insights with molecular data, this paper sheds light on the mechanisms driving oncocytic transformation and underscores the role of pathologists in identifying hereditary cancer syndromes.<\/jats:p>","DOI":"10.1159\/000545321","type":"journal-article","created":{"date-parts":[[2025,4,3]],"date-time":"2025-04-03T12:04:06Z","timestamp":1743681846000},"page":"474-487","source":"Crossref","is-referenced-by-count":0,"title":["Oncocytic Tumors in the Familial and Syndromic Contexts: A Tri-Focal Review \u2013 Integrated Cytopathological, Pathological, and Molecular Perspectives"],"prefix":"10.1159","volume":"69","author":[{"given":"Maria 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