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    蔡道章院长

    Custom Mod Mega1

    主任医师、教授、博导,南方医科大学第三附属医院(广东省骨科医院)院长

    • 中德骨科伤口管理学校校长
    • 广东省骨科研究院运动医学研究所所长
    • 广东省内运动医学专业唯一的博士研究生导师
    • 美国哈弗大学医学院骨科访问学者
    • 专业特长处于省内领先、国内或国际先进水平以上
    • 2018年获得“国之名医卓越建树”荣誉称号
    • 2017年被评为全国卫生计生系统先进工作者、广东省医学领军人才
    • 中国医师协会运动医师分会副会长
    • STCOT中国部运动医学分会副主任委员
    • 广东省医学会关节外科分会主任委员
    • 广东省医学会运动医学会分会名誉主任委员
    • 独立承担过国家“863”课题,主持过10余项省、部级科研项目
    • 多份专业杂志编委
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    • Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophyeepispadias complex 2026-09-16 00:00

      Glenda M. Beaman a,b, Adrian S. Woolf c,d, Filipa M. Lopes c, Shuang Andrew Guo e,f,g, J. Robert Harkness a,b, Raimondo M. Cervellione d, David Keene d, Imran Mushtaq h, Menna R. Clatworthy f,g,h, William G. Newman a,b,*

      Summary

      Introduction

      Bladder exstrophyeepispadias complex (BEEC) comprises a spectrum of anterior midline congenital malformations, involving the lower urinary tract. BEEC is usually sporadic, but families with more than one affected member have been reported, and a twin concordance study supported a genetic contribution to pathogenesis. Moreover, diverse chromosomal aberrations have been reported in a small subset of individuals with BEEC. The commonest are 22q11.2 microduplications, identified in approximately 3% of BEEC index cases.

      Objectives

      We aimed to refine the chromosome 22q11.2 locus, and to determine whether the encompassed genes are expressed in normal developing and mature human urinary bladders.

      Results

      Using DNA from an individual with CBE, the 22q11.2 duplicated locus was refined by identification of a maternally inherited 314 kb duplication (chr22:21,147,293e21,461,017), as depicted in this image. Moreover, the eight protein coding genes within the locus were found to be expressed during normal developing and mature bladders. To determine whether duplications in any of these individual genes were associated with CBE, we undertook copy number analyses in 115 individuals with CBE without duplications of the whole locus. No duplications of individual genes were found.

      Discussion

      The current study has refined the22q11.2locus associated with BEEC and has shown that the eight protein coding genes are expressed in human bladders both during antenatal development and postnatally. Nevertheless, the precise biological explanation as to why duplication of the phenocritical region of22q11 confers increased susceptibility to BEEC remains to be determined. The fact that individuals with CBE without duplications of the whole locus also lacked duplication of any of the individual genes suggests that in individuals with BEEC and duplication of the 22q11.2 locus altered dosage of more than one gene may be important in BEEC etiology.

      Conclusions

      The study has refined the 22q11.2 locus associated with BEEC and has shown that the eight protein coding genes within this locus are expressed in human bladders. 

    • W. Hardy Hendren, III, M.D., A personal perspective 2026-09-15 00:00
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  • 黄红军

黄红军

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15 11月 2019
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Author :   伤口世界
黄红军

擅长疾病 : 慢性创面修复,如压疮、糖尿病足、静脉性溃疡、放射性溃疡、开胸手术后切口不愈合、皮肤肿瘤、外伤后骨外露等。各种瘢痕及溃疡。

Latest from  伤口世界

  • Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophyeepispadias complex
  • W. Hardy Hendren, III, M.D., A personal perspective
  • 负压封闭引流技术在创面修复应用的专家共识(2025版)
  • Robotic retroperitoneal lymphadenectomy in paratesticular rhabdomyosarcoma
  • Robotic-assisted laparoscopic repair of a congenital rectourethral fistula with duplicated urethra

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  • 病情图文
  • 文献精选
  • 名医介绍
  • K2 Content
  • Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophyeepispadias complex 2026-09-16 00:00

    Glenda M. Beaman a,b, Adrian S. Woolf c,d, Filipa M. Lopes c, Shuang Andrew Guo e,f,g, J. Robert Harkness a,b, Raimondo M. Cervellione d, David Keene d, Imran Mushtaq h, Menna R. Clatworthy f,g,h, William G. Newman a,b,*

    Summary

    Introduction

    Bladder exstrophyeepispadias complex (BEEC) comprises a spectrum of anterior midline congenital malformations, involving the lower urinary tract. BEEC is usually sporadic, but families with more than one affected member have been reported, and a twin concordance study supported a genetic contribution to pathogenesis. Moreover, diverse chromosomal aberrations have been reported in a small subset of individuals with BEEC. The commonest are 22q11.2 microduplications, identified in approximately 3% of BEEC index cases.

    Objectives

    We aimed to refine the chromosome 22q11.2 locus, and to determine whether the encompassed genes are expressed in normal developing and mature human urinary bladders.

    Results

    Using DNA from an individual with CBE, the 22q11.2 duplicated locus was refined by identification of a maternally inherited 314 kb duplication (chr22:21,147,293e21,461,017), as depicted in this image. Moreover, the eight protein coding genes within the locus were found to be expressed during normal developing and mature bladders. To determine whether duplications in any of these individual genes were associated with CBE, we undertook copy number analyses in 115 individuals with CBE without duplications of the whole locus. No duplications of individual genes were found.

    Discussion

    The current study has refined the22q11.2locus associated with BEEC and has shown that the eight protein coding genes are expressed in human bladders both during antenatal development and postnatally. Nevertheless, the precise biological explanation as to why duplication of the phenocritical region of22q11 confers increased susceptibility to BEEC remains to be determined. The fact that individuals with CBE without duplications of the whole locus also lacked duplication of any of the individual genes suggests that in individuals with BEEC and duplication of the 22q11.2 locus altered dosage of more than one gene may be important in BEEC etiology.

    Conclusions

    The study has refined the 22q11.2 locus associated with BEEC and has shown that the eight protein coding genes within this locus are expressed in human bladders. 

  • W. Hardy Hendren, III, M.D., A personal perspective 2026-09-15 00:00
  • 负压封闭引流技术在创面修复应用的专家共识(2025版) 2026-09-14 00:00

    大湾区慢性创面医护康标准化体系建设联盟,《中国科技论文》体表外科卷编辑委员会,黄广涛1,吴 军1,郇京宁1,2

    (1.深圳大学第一附属医院(深圳市第二人民医院)烧伤整形科,广东深圳518000;2.上海交通大学医学院附属瑞金医院烧伤整形与创面修复科,上海200011)

    摘要:负压封闭引流技术(negative pressure wound therapy, NPWT)自2017年国内首部烧伤外科应用专家共识发布以来,其技术类型与临床应用范围均取得了显著拓展。特别是在促进各类急慢性创面愈合及预防外科手术部位感染方面,已累积了大量高质量循证证据。为整合国内外最新研究成果与临床实践经验,规范操作标准,提升治疗水平,国内创面修复相关多学科领域的专家共同撰写了本更新版共识。本共识汇聚了国内多位在创面相关的多学科领域的专家,结合国内外最新研究成果,遵循严谨的循证医学原则,采用系统综述方法,聚焦于NPWT的技术分类、适应症、参数优化及并发症处理等核心议题。工作小组系统检索了PubMed、Web of Science、IEEE Xplore及中国知网等数据库中2015—2025年相关文献,共获得791篇。经去重、筛选,并根据纳入标准(临床研究、随机对照试验、meta分析及相关共识等)最终纳入210篇文献进行证据综合与评价。本共识旨在为创面修复相关学科的临床医生提供基于最新证据、统一且可操作的治疗方案与技术规范。共识内容充分结合了我国临床实践的现状与需求,以期推动NPWT在国内的合理、规范及高效应用,最终惠及广大患者。

    关键词:负压封闭引流技术;手术部位感染;创面修复;手术切口并发症

    Expert consensus on the application of negative pressure wound therapy in wound repair (2025 Edition)
     
    Alliance for Standardized Construction of Chronic Wound Care and Rehabilitation in the Greater Bay Area, Editorial Committee of China Sciencepaper: Superficial Systems Surgery Volume, HUANG Guangtao1, WU Jun1, HUAN Jingning1,2
    (1. Department of Burn and Plastic Surgery, The First Affiliated Hospital of Shenzhen University (Shenzhen Second People’s Hospital), Shenzhen, Guangdong 518000, China;2. Department of Burn, Plastic Surgery and Wound Repair, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China)
     
    Abstract:Since the publication of the first domestic expert consensus on the application of negative pressure wound therapy (NPWT) in burn surgery in 2017, both the types of techniques and the scope of clinical applica⁃tions have significantly expanded. In particular, a substantial body of high-quality evidence has accumulated regarding its role in promoting the healing of various acute and chronic wounds and in preventing surgical site infections. To integrate the latest research findings and clinical experience both domestically and internationally,standardize operational protocols, and enhance treatment efficacy, a multidisciplinary group of domestic experts in wound repair jointly developed this updated consensus. This consensus brings together insights from multiple domestic experts in wound-related multidisciplinary fields, incorporates the latest research advances, adheres to rigorous evidence-based medicine principles, and employs systematic review methodology. It focuses on core issues related to NPWT, including technical classifications, indications, parameter optimization, and complica⁃tion management. The working group systematically searched relevant literature in databases including PubMed,Web of Science, IEEE Xplore, and the China National Knowledge Infrastructure (CNKI) published between 2015 and 2025, retrieving a total of 791 articles. After deduplication, screening, and applying inclusion criteria (clinical studies, randomized controlled trials, meta-analyses, and relevant consensus documents),210 articles were ultimately included for evidence synthesis and evaluation. This consensus aims to provide clinicians in wound repair-related disciplines with unified, actionable treatment protocols and technical standards based on the latest evidence. The content fully integrates the current status and needs of clinical practice in China, with the goal of promoting the rational, standardized, and efficient application of NPWT nationwide, ultimately benefiting a greater number of patients.
     
    Keywords:negative  pressure  wound  therapy;  surgical  site  infection;  wound  repair;  surgical  incision complications

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伤口世界平台生态圈,以“关爱人间所有伤口患者”为愿景,连接、整合和拓展线上和线下的管理慢性伤口的资源,倡导远程、就近和居家管理慢性伤口,解决伤口专家的碎片化时间的价值创造、诊疗经验的裂变复制、和患者的就近、居家和低成本管理慢性伤口的问题。

 

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2019广东省医疗行业协会伤口管理分会年会

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  • 2019年6月15日 中国广州
  • 主办单位:广东省医疗行业协会伤口管理分会

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