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海峡两岸医药卫生交流协会全科医学分会, 浙江省医学会全科医学分会, 浙江省数理医学学会全科未分化疾病专委会, 全科未分化疾病专家协作组, 中国老年医学学会. 多汗诊治与管理专家共识(2025)[J]. 中华全科医学, 2026, 24(4): 544-558. doi: 10.16766/j.cnki.issn.1674-4152.004438
引用本文: 海峡两岸医药卫生交流协会全科医学分会, 浙江省医学会全科医学分会, 浙江省数理医学学会全科未分化疾病专委会, 全科未分化疾病专家协作组, 中国老年医学学会. 多汗诊治与管理专家共识(2025)[J]. 中华全科医学, 2026, 24(4): 544-558. doi: 10.16766/j.cnki.issn.1674-4152.004438
General Practice Branch of Cross-Straits Medicine Exchange Association, General Practice Branch of Zhejiang Medical Association, Medically Unspecified Disease Professional Committee of Zhejiang Society for Mathematical Medicine, the Expert Collaboration Group on Medically Unspecified Disease in General Practice, Chinese Geriatrics Society. Expert consensus on the diagnosis, treatment, and management of hyperhidrosis (2025)[J]. Chinese Journal of General Practice, 2026, 24(4): 544-558. doi: 10.16766/j.cnki.issn.1674-4152.004438
Citation: General Practice Branch of Cross-Straits Medicine Exchange Association, General Practice Branch of Zhejiang Medical Association, Medically Unspecified Disease Professional Committee of Zhejiang Society for Mathematical Medicine, the Expert Collaboration Group on Medically Unspecified Disease in General Practice, Chinese Geriatrics Society. Expert consensus on the diagnosis, treatment, and management of hyperhidrosis (2025)[J]. Chinese Journal of General Practice, 2026, 24(4): 544-558. doi: 10.16766/j.cnki.issn.1674-4152.004438

多汗诊治与管理专家共识(2025)

doi: 10.16766/j.cnki.issn.1674-4152.004438
基金项目: 

国家自然科学基金项目 72274169

详细信息

    通信作者: 任菁菁,E-mail: 3204092@zju.edu.cn

  • 中图分类号: R442.9 R499

  • 摘要: 多汗是一种常见的临床表现,可单独或伴随系统性疾病出现,明显影响个体的日常生活、工作、社交及心理健康。当前,我国缺乏多汗的大规模流行病学数据,诊断标准与严重程度分级体系尚不统一,临床诊疗存在“同症不同判”的现象。本共识以多汗的诊治与管理为导向,系统阐述其定义、流行病学特征、病因与发病机制,综述诊断方法,包括详细问诊、体格检查、评估工具与诊断流程,并从治疗原则、治疗方案及治疗措施等方面展开详细的阐述。同时,本共识提出多汗的全程管理建议,涵盖社区管理、随访、双向转诊、健康教育与未来研究方向,旨在为全科医生及相关医务人员提供规范化、标准化的诊疗与管理指导,提升病因诊断准确率,优化治疗效果,改善患者生活质量。

     

  • 图  1  多汗治疗路径

    图  2  多汗社区管理流程图

    表  1  多汗严重程度量表(HDSS评分表)

    评分 症状描述 分度
    1分 从不明显,从不影响生活 轻度(1分)
    2分 可忍受,有时影响生活 中度(2分)
    3分 难以忍受,经常影响生活 重度(≥3分)
    4分 无法忍受,总是影响生活 重度(≥3分)
    下载: 导出CSV

    表  2  多汗的常见原因

    多汗分类 常见原因
      生理性多汗 环境温度高或衣物厚重、体力劳动和运动等;进食辛辣食物,饮用含酒精饮品或咖啡、浓茶等;特殊气味如香水等;情绪紧张、窘迫、恐惧、发怒、兴奋和精神打击等;婴儿期、月经期、妊娠期、产褥期、围绝经期等
      病理性多汗
        原发性多汗
          原发性全身性多汗 原发性多汗症
          原发性局限性多汗 手汗症、足汗症、腋汗症、头面汗症等
        继发性多汗
          继发性全身性多汗
            内分泌和代谢性疾病 甲状腺功能亢进、糖尿病、低血糖、垂体功能亢进、多囊卵巢综合征、维生素D缺乏、肥胖症等
            神经系统疾病 帕金森病、脑血管病、痴呆、多发性神经病、不宁腿综合征、下丘脑病变等
            循环系统疾病 心力衰竭、心肌梗死、休克、高血压、血管迷走性晕厥等
            呼吸系统疾病 慢性阻塞性肺疾病、支气管哮喘、呼吸衰竭、睡眠呼吸暂停低通气综合征等
            皮肤病 泛发性脓疱疮、脱发-多汗-舌状角膜混浊综合征(Spanlang-Tappeiner综合征)等
            风湿免疫病 系统性红斑狼疮、血管炎、类风湿性关节炎、Still病等
            血液系统疾病 淋巴瘤、多发性骨髓瘤、白血病、POEMS综合征、血色素沉积症等
            消化系统疾病 炎症性肠病、胃食管反流病、急性胃肠炎等
            肿瘤性疾病 嗜铬细胞瘤、肾上腺髓质瘤、中枢神经系统肿瘤、类癌、乳腺癌、肾癌、胆管癌等
            感染性疾病 结核病、布鲁氏菌病、心内膜炎、HIV感染、疟疾等
            精神心理疾病 焦虑症、抑郁症、精神分裂症、双相情感障碍、睡眠障碍等
            药物 具体药物见表 3
            其他 慢性酒精中毒、汞中毒,鸦片类、吗啡等麻醉品戒断等
          继发性局限性多汗
            神经系统疾病 带状疱疹后遗神经痛、糖尿病周围神经病变、脊髓疾病或损伤、交感神经干损伤、胸交感神经切除术后代偿性多汗、反射性交感神经萎缩、腮腺的手术或损伤如耳颞神经综合征(Frey’s综合征)、足部灼伤综合征(Gopalan综合征)、家族性自主神经失调综合征(Riley-Day综合征)、神经源性胸廓出口综合征、罗斯综合征(Ross综合征)等
            皮肤病 汗腺血管瘤样错构瘤、皮肤多发性神经病变、汗腺痣、先天性厚甲症、蓝色橡胶膜痣、单侧火焰痣、大疱性表皮松解症、甲-髌骨综合征等
            胸部肿瘤 肺癌、间皮瘤、脊髓瘤、骨瘤等
            其他 副肿瘤综合征、胫前黏液性水肿、尿道狭窄等
    注:部分继发性多汗病因存在全身性多汗和局限性多汗并存可能。
    下载: 导出CSV

    表  3  可致多汗的常见药物

    药物类别 代表药物
    神经、精神类药物 抗胆碱酯酶药物(多奈哌齐、卡巴拉汀、加兰他敏、石杉碱甲、溴吡斯的明、新斯的明等)、阿片类药(吗啡、羟考酮、芬太尼等)、选择性5-羟色胺再摄取抑制剂抗抑郁药(舍曲林、帕罗西汀、西酞普兰、艾司西酞普兰、氟西汀等)、三环类抗抑郁药(阿米替林、多塞平等)、5-羟色胺和去甲肾上腺素再摄取抑制剂抗抑郁药(文拉法辛、度洛西汀等)、单胺氧化酶抑制剂(苯乙肼等)、抗精神病药(氯氮平、奥氮平、利培酮、喹硫平等)、苯二氮类药(地西泮、阿普唑仑等)
    心血管、呼吸类药物 钙通道阻滞剂(硝苯地平、氨氯地平、非洛地平等)、β-受体阻滞剂(普萘洛尔、美托洛尔等)、α-受体阻滞剂(特拉唑嗪、多沙唑嗪等)、硝酸酯类药物(硝酸甘油、单硝酸异山梨酯等)、抗心律失常药(胺碘酮等)、β-受体激动剂(异丙肾上腺素、沙丁胺醇、特布他林等)
    内分泌类药物 降糖药(胰岛素、格列本脲、格列美脲、瑞格列奈等)
    消化类药物 奥美拉唑、甲氧氯普胺等
    激素类药物 甲状腺激素(左甲状腺素钠等)、皮质类固醇(泼尼松等)、抗雌激素类(他莫昔芬等)、抗雄激素类(比卡鲁胺、氟他胺等)、促性腺激素释放激素激动剂(亮丙瑞林、戈舍瑞林等)、芳香化酶抑制剂(阿那曲唑、来曲唑、依西美坦等)
    抗生素与抗病毒药物 广谱抗生素(左氧氟沙星、环丙沙星等)、抗结核药(利福平、异烟肼等)、抗病毒药(更昔洛韦等)
    非甾体类抗炎药 对乙酰氨基酚、布洛芬、萘普生、塞来昔布等
    其他药物 兴奋剂(哌甲酯、安非他命等)、抗青光眼药(毛果芸香碱滴眼液等)、钙调神经磷酸酶抑制剂(环孢素、他克莫司等)、肿瘤坏死因子抑制剂(英夫利西单抗、阿达木单抗等)、伊克珠单抗、舒尼替尼、帕博利珠单抗、度普利尤单抗等
    下载: 导出CSV

    表  4  多汗的RICE问诊

    问诊内容 提示信息
    R:患者本次就诊的主要原因(Reason)是什么? 明确多汗的特点及伴随症状
    I:患者认为自己出了什么问题(Idea)? 探寻多汗背后的可能原因及心理问题
    C:患者的担忧(Concern)是什么? 了解患者的真实诉求
    E:患者期望(Expectation)可以解决什么问题? 共同决策,了解患者对诊疗的接受程度
    下载: 导出CSV

    表  5  多汗的预警征及可能的严重疾病

    预警征 可能的严重疾病
    发热 感染性疾病等
    咳嗽、呼吸困难、咯血 肺结核、支气管扩张、慢性阻塞性肺疾病等
    呕血、黑便、便血 消化道出血
    心悸 甲状腺功能亢进、贫血等
    食欲亢进 糖尿病、甲状腺功能亢进等
    体重下降 糖尿病、甲状腺功能亢进、肺结核、恶性肿瘤等
    颈静脉怒张、端坐呼吸 急性心力衰竭、肺水肿等
    胸痛 急性冠脉综合征、主动脉夹层等
    行动迟缓、肢体抖动、活动障碍 脑卒中、脊髓损伤、帕金森病等
    皮肤水疱、溃破、脱屑 真菌感染等
    血压升高、头痛、面色苍白 嗜铬细胞瘤等
    情绪低落、情志改变、睡眠障碍 焦虑症、抑郁症、自主神经功能紊乱等
    下载: 导出CSV

    表  6  高级自主神经功能测试

    测试名称 类型 评估目标 方法 结果解释 备注
    热调节排汗测试(TST) 定性 评估全身汗腺节前和节后通路完整性 患者全身涂上遇湿变色的指示剂粉末(如茜素红),然后进入可控温腔室,通过逐渐升高核心体温来诱发全身性出汗 通过观察颜色变化的模式和分布,判断是否存在全身性或局灶性的出汗异常,从而定位神经损伤的区域 TST和QSART结合使用,能更精确地鉴别自主神经病变的部位[21]
    定量轴索反射泌汗测试(QSART) 定量 评估节后交感神经胆碱能纤维功能 通过离子导入法将乙酰胆碱导入皮肤特定部位,刺激汗腺产生轴索反射性出汗;使用汗液计测量和记录出汗量和延迟时间 定量评估汗腺功能
    下载: 导出CSV

    表  7  中医“汗证”辨证分型与舌脉特征

    中医证型 典型舌象 典型脉象 治疗原则
    肺卫不固 舌质淡,苔薄白 脉细弱或虚 益气固表
    营卫不和 舌质淡红,苔薄白 脉缓或浮缓 调和营卫
    阴虚火旺 舌质红或绛,少津,苔少或无苔 脉细数 滋阴降火,敛阴止汗
    邪热内蕴 舌质红,苔黄燥或黄腻 脉洪大有力或滑数 清胃泻热
    湿热蕴蒸 舌质红,苔黄腻 脉滑数或濡数 清热化湿,和营泄热
    气阴两虚 舌质红嫩,少津,苔薄白或少苔 脉细数或虚数 益气养阴,生津止汗
    气虚阳虚 舌质淡胖,边有齿痕,苔白滑或白腻 脉沉细无力或虚弱 益气温阳,固表止汗
    肝郁化火 舌质红,苔黄 脉弦数 疏肝清热
    脾虚湿困 舌质淡,苔白腻 脉濡缓 健脾化湿
    痰浊内阻 舌质淡,苔白腻 脉滑 化痰理气
    下载: 导出CSV

    表  8  实用的自我监测方法

    方法名称 操作步骤 结果观察 注意事项
    纸巾握持试验 1.取一张洁净干纸巾对折。2.受试者使用汗液分泌显著的手部紧握纸巾,持续1~2 min。 轻度:纸巾仅轻微潮湿,无浸润感。中度:纸巾被完全浸透,但无水滴形成。重度:纸巾完全湿透,并可见汗珠形成或滴落。 1.用于评估手汗症。2.测试前尽量保持手部干燥。3.在情绪稳定的状态下进行,以获得更准确的结果。
    淀粉-碘试验(家庭简易版) 1.于干燥待测皮肤区域均匀涂抹少量碘酊。2.自然风干后,均匀撒上一层薄玉米淀粉。 出汗区域的淀粉会与碘反应,呈现蓝色或紫黑色。颜色越深,说明该区域出汗越多;无颜色变化表示无汗。 对碘剂过敏者禁止使用。
    称重法 1.将干燥的纱布或滤纸称重(W1)。2.放在出汗部位一定时间(如5 min)吸收汗水,再次称重(W2)。 2次称重的重量差即为出汗量(W2-W1)。 可为治疗前后的疗效对比提供客观、量化的数据支持,但操作方法较烦琐。
    下载: 导出CSV
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