De Pasquale A, Ginaldi L, Di Leonardo G, Francavilla S, Quaglino D
Department of Internal Medicine, University of L'Aquila, Italy.
Ann Hematol. 1993 May;66(5):261-4. doi: 10.1007/BF01738477.
The authors describe a case of chronic myelomonocytic leukemia in which a myeloperoxidase (MPO) deficiency of circulating monocytes was first detected by automated differential cell counting, and subsequently confirmed by cytochemical and immunocytochemical investigations. MPO activity in neutrophil granulocytes from the same case was found to be normal. MPO deficiency in monocytes appeared to be associated with impaired phagocytic capacity and, based on the results of immunophenotypic and ultrastructural studies, was most likely attributable to a partial maturation arrest of monocytes. The present case suggests that MPO deficiency in myelodysplastic syndromes may have its origin in a number of different pathogenetic mechanisms.
作者描述了一例慢性粒单核细胞白血病病例,其中循环单核细胞的髓过氧化物酶(MPO)缺乏首先通过自动细胞分类计数检测到,随后通过细胞化学和免疫细胞化学研究得到证实。同一病例中性粒细胞的MPO活性正常。单核细胞中的MPO缺乏似乎与吞噬能力受损有关,并且根据免疫表型和超微结构研究结果,很可能归因于单核细胞的部分成熟停滞。本病例表明,骨髓增生异常综合征中的MPO缺乏可能源于多种不同的致病机制。