Dancey J T, Brubaker L H
Br J Haematol. 1979 Dec;43(4):607-17. doi: 10.1111/j.1365-2141.1979.tb03793.x.
Neutrophil marrow cellularity was determined in 14 neutropenic patients with rheumatoid arthritis (RA) from measurements of neutrophil-normoblast ratios in marrow biopsies and ferrokinetic estimates of marrow normoblasts. A marrow profile was developed for each patient comprising the numbers of promyelocytes and myelocytes, of metamyelocytes and bands, and of segmented neutrophils in whole marrow. In each case a maturation ratio was calculated by dividing the number of metamyelocytes and bands by the number of promyelocytes and myelocytes. The physiologic marrow response to loss of neutrophils from circulation was assumed to be an increase in promyelocytes and myelocytes due to proliferation and influx, a reduction in segmented cells due to early release, and a normal maturation ratio. The results were interpreted in the light of the 95% confidence limits for data previously obtained from 13 normal subjects: in patients with neutropenia reduced or basal numbers of promyelocytes and myelocytes were interpreted as absence of the anticipated proliferative response; increased numbers of marrow segmented cells were attributed to failure of release; a low maturation ratio was assessed to reflect intramedullary cell loss. The pattern in two patients with Felty's syndrome was consistent with a physiological response to neutrophil destruction. The other 12 patients had neutrophil marrow abnormalities. Seven patients with Felty's syndrome and four patients without splenomegaly had absolute or relative hypoplasia of neutrophil marrow or low maturation ratios. One patient with a normal spleen size had an increased number of marrow segmented cells yet failed to mobilize cells normally in response to dialysis coil-activation of C3. Abnormalities of neutrophil marrow may contribute to neutropenia in RA irrespective of the presence of splenomegaly. Recognition of neutrophil marrow abnormalities in these patients may be of value in prognosis and management.
通过对骨髓活检中中性粒细胞与早幼红细胞比例的测量以及骨髓早幼红细胞的铁动力学估计,确定了14例类风湿关节炎(RA)中性粒细胞减少患者的中性粒细胞骨髓细胞密度。为每位患者制定了骨髓图谱,包括全骨髓中早幼粒细胞和中幼粒细胞的数量、晚幼粒细胞和杆状核细胞的数量以及分叶核中性粒细胞的数量。在每种情况下,通过将晚幼粒细胞和杆状核细胞的数量除以早幼粒细胞和中幼粒细胞的数量来计算成熟率。假定骨髓对循环中中性粒细胞丢失的生理反应是由于增殖和流入导致早幼粒细胞和中幼粒细胞增加,由于早期释放导致分叶细胞减少,以及成熟率正常。根据先前从13名正常受试者获得的数据的95%置信限对结果进行解释:在中性粒细胞减少的患者中,早幼粒细胞和中幼粒细胞数量减少或处于基础水平被解释为缺乏预期的增殖反应;骨髓分叶细胞数量增加归因于释放失败;低成熟率被评估为反映髓内细胞丢失。两名费尔蒂综合征患者的模式与对中性粒细胞破坏的生理反应一致。其他12名患者有中性粒细胞骨髓异常。7名费尔蒂综合征患者和4名无脾肿大的患者有中性粒细胞骨髓绝对或相对发育不全或成熟率低。一名脾脏大小正常的患者骨髓分叶细胞数量增加,但在透析线圈激活C3时未能正常动员细胞。无论是否存在脾肿大,中性粒细胞骨髓异常可能导致RA患者中性粒细胞减少。认识到这些患者的中性粒细胞骨髓异常可能对预后和管理有价值。