D'Angelo Guido, Hotz Anna Maria, Todeschin Paolo
Laboratorio di Chimica-Clinica, Ematologia e Microbiologia, Ematologia/Coagulazione, Azienda Ospedaliera S. Antonio Abate-Gallarate, Varese, Italy.
Lab Hematol. 2008;14(1):7-9. doi: 10.1532/LH96.07018.
Acute lymphoblastic leukemia (ALL) associated with eosinophilia is very rare, with approximately 44 reported cases. We are reporting this case not only because of the rarity of ALL with peripheral blood eosinophilia, but also because we observed a homozygous deletion of the 9p21 locus corresponding to the p16 gene, a cytogenetic abnormality that was not reported in other documented cases. ALL with eosinophilia must be considered a distinct clini-copathologic entity. It is very important for clinicians to be aware of this specific manifestation of ALL within the context of a persistent peripheral eosinophilia, particularly if no lymphoblasts are present in the peripheral blood.
与嗜酸性粒细胞增多相关的急性淋巴细胞白血病(ALL)非常罕见,仅有约44例报道。我们报告此病例,不仅是因为外周血嗜酸性粒细胞增多伴ALL罕见,还因为我们观察到对应p16基因的9p21位点存在纯合缺失,这一细胞遗传学异常在其他已记录病例中未见报道。嗜酸性粒细胞增多性ALL必须被视为一种独特的临床病理实体。临床医生必须意识到,在持续性外周血嗜酸性粒细胞增多的情况下,ALL会有这种特殊表现,特别是在外周血中不存在原始淋巴细胞时,这一点非常重要。