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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
In this case, we present RDD with the parotid gland, mediastinum, and cardiac involvement.
📌 3 Key Takeaways
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Objective & Hypothesis:Rosai–Dorfman disease (RDD) is a benign form of histiocyte proliferation with unknown etiology that was first described by Rosai–Dorfman in 1969 (1).
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Key Findings & Data:RDD is mostly presented with cervical lymphadenopathy, and also involves the extranodal system including skin, nasal cavity and paranasal sinuses, orbit, upper respiratory tract, and bone (2).
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Conclusion & Impact:In this case, we present RDD with the parotid gland, mediastinum, and cardiac involvement.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Özet
Rosai–Dorfman disease (RDD) is a benign form of histiocyte proliferation with unknown etiology that was first described by Rosai–Dorfman in 1969 (1). RDD is mostly presented with cervical lymphadenopathy, and also involves the extranodal system including skin, nasal cavity and paranasal sinuses, orbit, upper respiratory tract, and bone (2). RDD rarely involves the heart. There are only 19 reported cases of RDD in the literature, with none involving the right ventricle. In this case, we present RDD with the parotid gland, mediastinum, and cardiac involvement.
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Cite This Article
YAMAN, B., CERİT, L., KEMAL, H. S., USALP, S., DUYGU, H. (2019). Unusual involvement of right ventricle in patient with Rosai–Dorfman disease. The Anatolian Journal of Cardiology, Cilt: 22 - Sayı: 5, 271–272. https://ajindex.com/articles/366793