Mild Hereditary Spherocytosis without Accompanying Hereditary Haemochromatosis: An Unrecognised Cause of Iron Overload

被引:3
|
作者
Tole, Soumitra [1 ]
Amid, Ali [2 ]
Baker, Jillian [1 ,3 ,4 ]
Kuo, Kevin [5 ]
Pugi, Jakob [1 ]
Carcao, Manuel [1 ,6 ]
机构
[1] Hosp Sick Children, Dept Paediat, Div Haematol Oncol, Toronto, ON, Canada
[2] Childrens Hosp Eastern Ontario, Dept Paediat, Div Haematol Oncol, Ottawa, ON, Canada
[3] St Michaels Hosp, Dept Paediat, Toronto, ON, Canada
[4] St Michaels Hosp, Dept Med, Div Haematol Oncol, Toronto, ON, Canada
[5] Univ Hlth Network, Dept Med, Div Haematol Oncol, Toronto, ON, Canada
[6] Hosp Sick Children, Res Inst, Child Hlth Evaluat Sci, Toronto, ON, Canada
关键词
Spherocytosis; Iron overload; Hereditary haemochromatosis; ERYTHROFERRONE; ABSORPTION; HEPCIDIN;
D O I
10.1159/000497175
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hereditary spherocytosis (HS) is a common inherited haemolytic anaemia and has great variability in its presentation. Non-transfusion iron overload in HS has only been reported with co-inheritance of hereditary haemochromatosis (HHC). We present 4 unrelated patients of East Asian ethnicity with mild HS and significant non-transfusion iron overload in the absence of known disease-causing mutations in HHC genes. We hypothesise that, in patients with mild HS, life-long chronic haemolysis and erythropoietic drive may promote iron absorption. This suggests that mild HS may not be entirely benign, and that patients with mild HS should be monitored for iron overload. (c) 2019 S. Karger AG, Basel
引用
收藏
页码:256 / 260
页数:5
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