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病例报告:单孔胸腔镜手术治疗一名9岁儿童的重度原发性手掌多汗症。

Case Report: Single-port thoracoscopic surgery for severe primary palmar hyperhidrosis in a 9-year-old child.

作者信息

Luo Zhen, Li Yu, Zhou Guangxu, Mao Kaiyi, Tan Hongyang, Zhao Peng, Li Yingbo, Shang Xianhui, Ma Hong, Wang Cao

机构信息

Department of Pediatric Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.

Guizhou Children's Hospital, Zunyi, Guizhou, China.

出版信息

Front Med (Lausanne). 2025 Apr 15;12:1542064. doi: 10.3389/fmed.2025.1542064. eCollection 2025.

Abstract

Primary palmar hyperhidrosis (PPH) is a somatic condition characterized by excessive sweating of the hands. It mainly affects adolescents and young adults and is rarely observed among children. This condition significantly impairs patients' academic performance, daily activities, and social interactions and can even lead to insurmountable psychological burdens. Surgical intervention for PPH is typically reserved for individuals aged 16 years and older, as compensatory hyperhidrosis occurs at a high rate (65%) postoperatively among children younger than 14 years. Therefore, the decision for surgery is controversial and has been rarely documented in the literature. Here, we report a 9-year-old child with a 3-year history of bilateral palmar hyperhidrosis. Conservative treatment with medications for 6 months led to no improvement. The patient had signs of low self-esteem, social withdrawal, and aversion to school, alongside recurrent skin damage at the fingertips. Both the child and parents expressed a strong desire for effective treatment. Single-port endoscopic thoracic sympathectomy (ETS) was conducted after comprehensive risk disclosure and obtaining informed consent from the parents, achieving remarkable therapeutic outcomes. At the 12-month follow-up, the patient exhibited no recurrence of symptoms, no compensatory hyperhidrosis, and no complications, such as Horner's syndrome. Both hands remained warm and dry, the lesions of fingertip skin healed, and the patient's personality became noticeably more positive. Furthermore, the surgical incision was aesthetically pleasing.

摘要

原发性手掌多汗症(PPH)是一种以手部过度出汗为特征的躯体疾病。它主要影响青少年和年轻人,在儿童中很少见。这种情况会严重损害患者的学业成绩、日常活动和社交互动,甚至会导致难以承受的心理负担。PPH的手术干预通常适用于16岁及以上的个体,因为14岁以下儿童术后代偿性多汗症的发生率很高(65%)。因此,手术决策存在争议,且在文献中鲜有记载。在此,我们报告一名9岁儿童,有3年双侧手掌多汗症病史。药物保守治疗6个月未见改善。患者有自卑、社交退缩和厌学迹象,同时指尖反复出现皮肤损伤。患儿及其父母都强烈希望得到有效治疗。在全面披露风险并获得家长知情同意后,进行了单孔胸腔镜交感神经切除术(ETS),取得了显著的治疗效果。在12个月的随访中,患者症状未复发,无代偿性多汗症,也无霍纳综合征等并发症。双手保持温暖干燥,指尖皮肤损伤愈合,患者的性格明显变得更加积极。此外,手术切口美观。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b7/12037579/803d25d09559/fmed-12-1542064-g0001.jpg

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