Prokocimer M, Inbal A, Gelber M, Shohat B, Ben Basat M, Shaklai M
Acta Haematol. 1985;74(3):164-7. doi: 10.1159/000206198.
We describe a patient with hemophagocytic syndrome resembling malignant histiocytosis which was complicating myelodysplastic disease of 3 years duration. Detailed morphological and ultrastructural studies indicate that the histiocytic component did not demonstrate features of malignancy. A review of other known malignancies ending up in the hemophagocytic syndrome is given, and the significance of this syndrome is discussed.
我们描述了一名患有噬血细胞综合征的患者，该综合征类似于恶性组织细胞增多症，是持续3年的骨髓增生异常疾病的并发症。详细的形态学和超微结构研究表明，组织细胞成分未显示恶性特征。本文回顾了其他最终导致噬血细胞综合征的已知恶性肿瘤，并讨论了该综合征的意义。
