Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report

被引：1
|
作者：
Le Guyader, Mailys [1 ]
Pineau-Vincent, Fabienne [1 ]
Lemaire, Pierre [1 ]
机构：
[1] Ctr Hosp, Lab Hematol & Immunol, Le Mans, France
来源：
ANNALES DE BIOLOGIE CLINIQUE | 2016年 / 74卷 / 01期
关键词：
flow cytometry; paroxysmal nocturnal hemoglobinuria; FLOW-CYTOMETRIC ANALYSIS; BLOOD; DIAGNOSIS; ASSAY;
D O I：
10.1684/abc.2015.1117
中图分类号：
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号：
1001 ;
摘要：
Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytopenia with multilineage dysplasia.
引用
收藏
页码：106 / 109
页数：4
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