Bozdech M J, Bainton D F, Mustacchi P
Am J Clin Pathol. 1980 Mar;73(3):409-16. doi: 10.1093/ajcp/73.3.409.
Partial peroxidase deficiency was discovered by means of automated continuous-flow cytochemistry (Hemalog D) in the neutrophils and eosinophils of a patient admitted for evaluation of the gradual onset of intellectual deterioration. Wright's stain and routine benzidine peroxidase reaction on peripheral blood smears showed a normal differential count and peroxidase activity, respectively, but smears stained for peroxidase using 4-chloro-1-naphthol, the reagent used in Hemalog D, showed absence of enzymatic activity in neutrophils and eosinophils. Electron microscopy using the Graham-Karnovsky diamino-benzidine method confirmed these findings, demonstrating a new pattern of peroxidase deficiency in which a decreased number of peroxidase-positive granules were found in all neutrophils and, surprisingly, also in eosinophils. Bio-chemical studies also showed that the apparent deficiency is due to an abnormal proportion of "insoluble" peroxidase. These results and the clinical findings for the patient are consistent with the diagnosis of ceroid lipofuscinosis (Kuf's disease).
通过自动连续流式细胞化学法(Hemalog D)在一名因智力逐渐衰退入院评估的患者的中性粒细胞和嗜酸性粒细胞中发现了部分过氧化物酶缺乏。外周血涂片上的瑞氏染色和常规联苯胺过氧化物酶反应分别显示正常的分类计数和过氧化物酶活性,但使用Hemalog D中所用试剂4-氯-1-萘酚进行过氧化物酶染色的涂片显示中性粒细胞和嗜酸性粒细胞中无酶活性。使用格雷厄姆-卡诺夫斯基二氨基联苯胺法的电子显微镜检查证实了这些发现,显示出一种新的过氧化物酶缺乏模式,即所有中性粒细胞以及令人惊讶的是嗜酸性粒细胞中过氧化物酶阳性颗粒数量减少。生化研究还表明,明显的缺乏是由于“不溶性”过氧化物酶比例异常所致。这些结果以及该患者的临床发现与类蜡样脂褐质沉积症(库夫病)的诊断一致。