Lardhi Amer A, Al-Mutairi Abdullah K, Al-Qahtani Mohammed H, Al-Mutairi Atheer K
King Fahad Hospital of the University, Faculty of Medicine, Imam Abdulrahman bin Faisal University, AL-Khobar, Saudi Arabia.
Case Rep Oncol. 2018 Jan 19;11(1):55-62. doi: 10.1159/000485968. eCollection 2018 Jan-Apr.
Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented with fever, pallor, and generalized lymphadenopathy complicated by the development of autoimmune hemolytic anemia. A review of the literature of this condition is also provided.
罗萨伊-多夫曼病是一种罕见的组织细胞增生性疾病，通常表现为巨大淋巴结病和多种全身症状。严重溶血性贫血是该疾病罕见的并发症。尽管该病的病因尚不清楚，但包括病毒在内的感染因素被认为与之有关。我们报告一名2岁女童，她出现发热、面色苍白和全身淋巴结病，并并发自身免疫性溶血性贫血。本文还对该疾病的文献进行了综述。
