摘要
报道1例儿童重型β地中海贫血合并肝硬化病例,患者婴儿期确诊为重型β地中海贫血,长期输血治疗,后诊断为铁过载,因祛铁治疗不规范8岁多即出现消化道功能障碍、肝硬化,属于罕见病例。患儿起病年龄小,本病例报道旨在引发我们对儿童重型地中海贫血铁过载及其规范治疗的再思考和重视。
This study reports a case of β-Thalassemia Major combined with cirrhosis in a child. The patient was diagnosed with β-Thalassemia Major during infancy and was later diagnosed with iron overload after long-term blood transfusion treatment. The child developed digestive tract dysfunction and cirrhosis in 8 years due to non-standard iron chelation. This case is a rare case. The onset age of the patient is young, and this case report aims to provoke further reflection and attention on iron overload and standardized treatment of severe thalassemia in children.
出处
《临床医学进展》
2024年第4期325-330,共6页
Advances in Clinical Medicine
