組織細胞性髓性網狀細胞增多症是一种網狀內皮系統的增生性疾病。1939年Scott和Robb-Smith自一类所謂“非典型性何杰金氏病”中区別出一部分具有一定的临床表現和病理变化的病例,收集了过去文献中的六例并报告了四个新的病例。这种疾病的监床特点为发热、消瘦、 Histocytic myelocytosis is a proliferative disorder of the reticuloendothelial system. In 1939, Scott and Robb-Smith distinguished a group of cases with certain clinical manifestations and pathological changes from the so-called “atypical Hodgkin’s disease.” Six cases in the past were collected and four new reports were reported Of cases. The clinical features of this disease are fever, weight loss,