Gerritsen Annemieke, Lam King, Marion Schneider E, van den Heuvel-Eibrink Marry M
Department of Pediatric Oncology/Hematology, Erasmus University Medical Center, Sophia Children's Hospital, Rotterdam, The Netherlands.
Leuk Res. 2006 Oct;30(10):1299-303. doi: 10.1016/j.leukres.2005.12.027. Epub 2006 Feb 17.
We present a case of juvenile myelomonocytic leukemia (JMML) accompanied by immune-mediated hemophagocytic lymphohistiocytosis (HLH) and Kikuchi's disease, both as a paraneoplastic phenomenon. As this combination, to the best of our knowledge, has not been described before, consensus on preferable treatment is lacking. Our patient was treated with prednisolone according to the few described cases of HLH and Kikuchi's disease in non-JMML patients, resulting in disappearance of the clinical symptoms.
我们报告了一例青少年粒单核细胞白血病(JMML),其伴有免疫介导的噬血细胞性淋巴组织细胞增生症(HLH)和菊池病,二者均为副肿瘤现象。据我们所知,这种组合此前尚未有过描述,因此缺乏关于首选治疗方法的共识。我们的患者根据非JMML患者中少数已报道的HLH和菊池病病例接受了泼尼松龙治疗,临床症状消失。