• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Epidermolysis bullosa simplex generalisata: importance of immunofluorescence studies in early diagnosis.

作者信息

Baker H

出版信息

Arch Dermatol Res. 1982;272(3-4):393-9. doi: 10.1007/BF00509071.

DOI:10.1007/BF00509071
PMID:6762155
Abstract

An unusual case of severe generalized epidermolysis bullosa (EB) simplex is described. Its severity, oral involvement and early milia formation suggested a dystrophic form of the disease, but early immunofluorescence studies on skin biopsy material using bullous pemphigoid (BP) serum clearly showed the level of cleavage to be superficial to the dermo-epidermal junction and microscopy confirmed this. The diagnosis of EB simplex was thus quickly established allowing conservative treatment to be pursued with confidence, and preventing unnecessary exposure of the child to systemic corticoid or phenytoin therapy.

摘要

相似文献

1
Epidermolysis bullosa simplex generalisata: importance of immunofluorescence studies in early diagnosis.
Arch Dermatol Res. 1982;272(3-4):393-9. doi: 10.1007/BF00509071.
2
Epidermolysis bullosa: variability of expression of cicatricial pemphigoid, bullous pemphigoid, and epidermolysis bullosa acquisita antigens in clinically uninvolved skin.大疱性表皮松解症:瘢痕性类天疱疮、大疱性类天疱疮及获得性大疱性表皮松解症抗原在临床未受累皮肤中的表达变异性
J Invest Dermatol. 1985 Jul;85(1):47-9. doi: 10.1111/1523-1747.ep12275025.
3
The generalized atrophic benign form of junctional epidermolysis bullosa. Experience with four patients in the United States.交界性大疱性表皮松解症的全身性萎缩良性型。美国4例患者的经验。
Arch Dermatol. 1986 Jun;122(6):704-10.
4
Epidermolysis bullosa acquisita: an autoimmune disease with distinctive immunoultrastructural features.获得性大疱性表皮松解症:一种具有独特免疫超微结构特征的自身免疫性疾病。
Cutis. 1983 Dec;32(6):521-7.
5
Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases.常染色体隐性单纯性大疱性表皮松解症。具有提示交界性或营养不良性大疱性表皮松解症的全身性表型特征,且与神经肌肉疾病相关。
Arch Dermatol. 1989 Jul;125(7):931-8. doi: 10.1001/archderm.125.7.931.
6
Epidermolysis bullosa acquisita: ultrastructural and immunological studies.获得性大疱性表皮松解症:超微结构与免疫学研究。
J Invest Dermatol. 1981 Apr;76(4):288-92. doi: 10.1111/1523-1747.ep12526124.
7
Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases.机械性大疱性疾病中真皮-表皮交界处抗原决定簇的免疫荧光定位
J Invest Dermatol. 1981 Feb;76(2):113-8. doi: 10.1111/1523-1747.ep12525447.
8
Epidermolysis bullosa acquisita with negative direct immunofluorescence.直接免疫荧光检查阴性的获得性大疱性表皮松解症
Arch Dermatol. 1985 Sep;121(9):1183-5.
9
Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosis.
Br J Dermatol. 1986 Aug;115(2):125-31. doi: 10.1111/j.1365-2133.1986.tb05707.x.
10
[The dermo-epidermal junction and its acquired and hereditary pathology. A few recent advances].[真皮-表皮连接及其获得性和遗传性病理学。一些近期进展]
Pathol Biol (Paris). 1992 Feb;40(2):121-32.

本文引用的文献

1
Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases.机械性大疱性疾病中真皮-表皮交界处抗原决定簇的免疫荧光定位
J Invest Dermatol. 1981 Feb;76(2):113-8. doi: 10.1111/1523-1747.ep12525447.
2
The management of esophageal complications of epidermolysis bullosa.
Am J Dig Dis. 1972 Oct;17(10):875-80. doi: 10.1007/BF02239525.
3
Ultrastructural studies in epidermolysis bullosa heriditaria. I. Dominant dystrophic type of Pasini.遗传性大疱性表皮松解症的超微结构研究。I. 帕西尼显性营养不良型。
Arch Dermatol Forsch. 1975;252(3):167-78.
4
Ultrastructural localization of immunoglobulins in bullous pemphigoid skin. Employment of a new peroxidase-antiperoxidase multistep method.
J Invest Dermatol. 1975 Apr;64(4):220-7. doi: 10.1111/1523-1747.ep12510658.
5
Ultrastructural studies in epidermolysis bullosa hereditaria. IV. Recessive dystrophic types with junctional blistering. (Infantile or Herlitz-Pearson type and adult type).
Arch Dermatol Res (1975). 1976 Nov 26;257(1):17-32. doi: 10.1007/BF00569110.
6
Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine.遗传性大疱性表皮松解症的超微结构研究。II. 科凯恩和图赖讷显性营养不良型
Arch Dermatol Res (1975). 1976 Jun 21;255(3):285-95. doi: 10.1007/BF00561499.
7
Epidermolysis bullosa hereditaria letalis: pathology, natural history and therapy.遗传性致死性大疱性表皮松解症:病理学、自然病史与治疗
Br J Dermatol. 1977 Jan;96(1):51-8. doi: 10.1111/j.1365-2133.1977.tb05185.x.
8
Epidermolysis bullosa--new therapeutic approaches.大疱性表皮松解症——新的治疗方法。
Australas J Dermatol. 1978 Apr;19(1):1-8. doi: 10.1111/j.1440-0960.1978.tb00177.x.