A Rare Case of Hb H Disease and Systemic Lupus Erythematosus

被引：1
|
作者：
Lin, Qi-Yin [1 ]
Chen, Di-Yu [1 ]
Kong, Shu [1 ]
Liu, Wei-Qiang [1 ]
Sun, Xiao-Fang [1 ]
Li, Dong-Zhi [2 ]
机构：
[1] Guangzhou Med Univ, Affiliated Hosp 3, Dept Fetal Med & Prenatal Diag, Thalassemia Diagnost Lab, Guangzhou, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Prenatal Diagnost Ctr, Guangzhou, Peoples R China
来源：
HEMOGLOBIN | 2021年 / 45卷 / 01期
关键词：
α -Thalassemia (α -thal); Hb H disease; systemic lupus erythematosus (SLE);
D O I：
10.1080/03630269.2021.1886945
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Anemia is common in patients with systemic lupus erythematosus (SLE). The association between thalassemia and SLE is rare. In this study, we report the first patient who was found to have a severe hemolytic anemia caused by combination of SLE and Hb H disease. The patient had a more severe presentation in the hematological system. Our case indicates that for a patient who was diagnosed with SLE and developed deterioration in her hematological cell lines, investigation of other possible coexisting causes would be warranted.
引用
收藏
页码：66 / 68
页数：3
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