[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$f65-g5LTUgHIk8dGZIHhGe2pKpxnfW0g-O4HGxk3yxcs":3,"$fLxR47h5ptAzKGgB5RdopxO5DEvOPtJH6hwVRcUv-vqQ":8},{"code":4,"msg":5,"message":6,"data":6,"success":7},401,"认证失败，无法访问系统资源",null,false,{"code":9,"msg":10,"message":6,"data":11,"success":35},200,"操作成功",{"id":12,"name":13,"describes":6,"symptoms":6,"checkup":6,"treatment":6,"seoTitle":14,"seoKeywords":15,"seoDescription":16,"coverVertical":6,"coverAcross":6,"introduceClassifications":17,"departments":33},3109,"先天自愈性朗格汉斯组织细胞增"," 先天自愈性朗格汉斯组织细胞增相关信息与治疗\n"," 先天自愈性朗格汉斯组织细胞增, 朗格汉斯细胞增生症, 朗格汉斯组织细胞增治疗, 自愈性疾病\n"," 了解先天自愈性朗格汉斯组织细胞增的详细信息，包括症状、诊断和治疗方法，探索自愈性疾病的特点及如何有效管理病情。",[18,23,28],{"id":19,"classification":20,"description":21,"sort":22,"diseaseId":12},138613,"概述","\u003Cp>　　先天自愈性朗格汉斯组织细胞增生症(Congenital Self-Healing langerhans Histiocytosis，CSLH)又名先天性自愈性网状组织细胞增生症(Congenital self-healing reticulohistiocytosis)本病于1973年由Hashimoto和Pritzker报告，故又名Hashimoto-Pritzker病，呈自限性、良性经过，仅有皮损而无系统性损害;其皮肤损害特点和组织病理象，实际上与朗格汉斯细胞组织细胞增生症相似，免疫组化检查S-100蛋白，CDIa(OKT6)亦阳性，且超微检查也可见到Birbeck颗粒;因而有人将本病列入朗格汉斯组织细胞增生症病谱中的最良性型。\u003C/p>",0,{"id":24,"classification":25,"description":26,"sort":27,"diseaseId":12},138614,"症状","\u003Cp>　　常见症状：结节、溃疡、黏膜损害、组织细胞增生\u003C/p>",1,{"id":29,"classification":30,"description":31,"sort":32,"diseaseId":12},138615,"检查","\u003Cp>　　检查项目：血常规、涂片、组织病理\u003C/p>\u003Cp>　　免疫组化检查：S-100蛋白和CDIa(OKT6)阳性。超微检查10%～25%细胞，可见Birbeck颗粒。大的组织细胞外观的细胞内含致密小体，规则性板层小体和独特的吞噬溶酶体。\u003C/p>",2,[34],"皮肤科",true]