Weiss Douglas J
Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN 55108, USA.
J Am Vet Med Assoc. 2006 Mar 15;228(6):893-7. doi: 10.2460/javma.228.6.893.
To further classify dysmyelopoiesis as diagnosed by use of a general classification scheme and to determine clinical features and laboratory test results that could be used to differentiate between the various forms of dysmyelopoiesis in cats.
Retrospective case series. Sample Population-Bone marrow slides from 34 cats.
Medical records of cats in which dysmyelopoiesis was diagnosed on the basis of blood and bone marrow analyses from 1996 to 2005 were reviewed. Criteria for inclusion in the study were findings of > 10% dysplastic cells in 1 or more hematologic cell lines in the bone marrow and concurrent cytopenias in the blood. Cats that met these criteria were classified into subcategories of myelodysplastic syndromes or secondary dysmyelopoiesis on the basis of reevaluation of slides.
Of 189 bone marrow slides reviewed, 34 (14.9%) had > 10% dysplastic cells in 1 or more cell lines. Cats were subcategorized as having myelodysplastic syndrome with excessive numbers of blast cells (n = 13), myelodysplastic syndrome with refractory cytopenias (8), a variant form of myelodysplastic syndrome (1), and secondary dysmyelopoiesis (12). Findings of dysmyelopoiesis and autoagglutination in cats with myelodysplastic syndrome and in those with immune-mediated anemia complicated differentiating between the 2 conditions.
Differentiating cats with myelodysplastic syndromes from cats with immune-mediated hemolytic anemia was difficult because severe anemia and autoagglutination may be concurrent findings in both conditions. Differentiating between myelodysplastic syndrome with excessive numbers of blast cells and myelodysplastic syndrome with refractory cytopenias was useful in predicting clinical outcome.
使用通用分类方案进一步对骨髓生成异常进行分类,并确定可用于区分猫的各种骨髓生成异常形式的临床特征和实验室检查结果。
回顾性病例系列。样本群体——34只猫的骨髓涂片。
回顾1996年至2005年期间根据血液和骨髓分析诊断为骨髓生成异常的猫的病历。纳入研究的标准是骨髓中1种或更多血液学细胞系中发育异常细胞>10%,且血液中同时存在血细胞减少。符合这些标准的猫根据涂片重新评估被分类为骨髓增生异常综合征或继发性骨髓生成异常的亚类。
在189张回顾的骨髓涂片中,34张(14.9%)在1种或更多细胞系中有>10%的发育异常细胞。猫被亚分类为有大量原始细胞的骨髓增生异常综合征(n = 13)、难治性血细胞减少的骨髓增生异常综合征(8只)、骨髓增生异常综合征的一种变异形式(1只)和继发性骨髓生成异常(12只)。骨髓增生异常综合征的猫和免疫介导性贫血的猫中骨髓生成异常和自身凝集的发现使区分这两种情况变得复杂。
区分骨髓增生异常综合征的猫和免疫介导性溶血性贫血的猫很困难,因为严重贫血和自身凝集可能是这两种情况的共同表现。区分有大量原始细胞的骨髓增生异常综合征和难治性血细胞减少的骨髓增生异常综合征有助于预测临床结果。