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三名慢性溶血性贫血儿童感染细小病毒B19,临床表现类似骨髓增生异常综合征。

Parvovirus B19 infection reminiscent of myelodysplastic syndrome in three children with chronic hemolytic anemia.

作者信息

Yarali N, Duru F, Sipahi T, Kara A, Teziç T

机构信息

Department or Pediatric Hematology, Dr. Sami Ulus Children's Disease Centre, Ankara, Turkey.

出版信息

Pediatr Hematol Oncol. 2000 Sep;17(6):475-82. doi: 10.1080/08880010050120836.

Abstract

The authors have seen transient pancytopenia with erythroid hypoplasia and striking trilineage myelodysplasia reminiscent of true myelodysplastic syndrome (MDS) in 3 children, 1 with thalassemia intermedia and the other 2 with previously undiagnosed hereditary spherocytosis. In these 3 children transient pancytopenia and myelodysplasia coincided with serological evidence of acute parvovirus-B19 (PV-B19) infection, strongly suggesting their relevance. It is of interest that these 3 cases were encountered within a period of 6 months. This might be an incidental event, but it might also be concluded that acute PV-B19 infection associated transient pancytopenia with morphological appearance of MDS may occur more frequently than reported in the literature. So, PV-B19-associated nonclonal MDS should be considered in the differential diagnosis of true clonal MDS.

摘要

作者们在3名儿童中发现了伴有红系造血低下的短暂全血细胞减少以及显著的三系骨髓发育异常,这让人联想到真正的骨髓增生异常综合征(MDS)。其中1名患有中间型地中海贫血,另外2名患有此前未诊断出的遗传性球形红细胞增多症。在这3名儿童中,短暂全血细胞减少和骨髓发育异常与急性细小病毒B19(PV-B19)感染的血清学证据同时出现,强烈提示它们之间的关联。有趣的是,这3例病例在6个月内出现。这可能是偶然事件,但也可以得出结论,急性PV-B19感染相关的短暂全血细胞减少伴MDS形态学表现可能比文献报道的更频繁发生。因此,在真正的克隆性MDS的鉴别诊断中应考虑PV-B19相关的非克隆性MDS。

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