Khanna Surendra Nath, Iyer Krishna Subramony, Paul Mathews, Radhakrishnan S, Rathi Arun K
Fortis Escorts Heart Institute, New Delhi, India.
Fortis Escorts Heart Institute, New Delhi, India.
Ann Thorac Surg. 2017 May;103(5):e443-e445. doi: 10.1016/j.athoracsur.2016.09.105.
Rosai-Dorfman disease, or sinus histiocytosis with massive lymphadenopathy, is a rare multisystemic disorder that was first reported by Rosai and Dorfman in 1969. It is a distinct histioproliferative disorder due to overproduction of histiocytes, which accumulate in lymph nodes. The cardiac involvement of this disease is extremely rare, and until now, only 18 cases have been reported. We report the case of a 53-year-old woman with right atrial mass mimicking myxoma, which the histopathologic evaluation revealed to be Rosai-Dorfman disease of the right atrium.
罗萨伊-多夫曼病,即伴巨大淋巴结病的窦性组织细胞增多症,是一种罕见的多系统疾病,于1969年由罗萨伊和多夫曼首次报道。它是一种独特的组织细胞增生性疾病,由于组织细胞过度产生并积聚在淋巴结中。这种疾病累及心脏极为罕见,截至目前,仅报道过18例。我们报告一例53岁女性,其右心房肿物酷似黏液瘤,组织病理学评估显示为右心房罗萨伊-多夫曼病。