• 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

皮肤非X组织细胞增多症:临床与组织学特征及对皮肤磨削术的反应

Cutaneous non-X histiocytosis: clinical and histologic features and response to dermabrasion.

作者信息

Fowler J F, Callen J P, Hodge S J, Verdi G

出版信息

J Am Acad Dermatol. 1985 Oct;13(4):645-9. doi: 10.1016/s0190-9622(85)70209-5.

DOI:10.1016/s0190-9622(85)70209-5
PMID:3841133
Abstract

A 22-year-old man presented with a progressive cutaneous eruption consisting of reddish-yellow papules and plaques on his face, which was histopathologically characteristic of a non-X histiocytosis. No systemic involvement was present. Monoclonal antibody staining of the tissue infiltrate was strongly positive for only OKT6. On electron microscopy, Langerhans (Birbeck) granules were not found. Four years of conservative treatment was unsuccessful. Spontaneous involution did not occur. Dermabrasion not only produced excellent cosmetic results, but on rebiopsy the histiocytic infiltrate was absent. There has been no recurrence in treated areas after 18 months.

摘要

一名22岁男性患者,面部出现进行性皮肤疹,表现为红黄丘疹和斑块,组织病理学特征为非X组织细胞增生症。无全身受累情况。组织浸润的单克隆抗体染色仅对OKT6呈强阳性。电子显微镜检查未发现朗格汉斯(Birbeck)颗粒。四年的保守治疗未成功。皮疹未自发消退。皮肤磨削术不仅取得了极佳的美容效果,而且再次活检时组织细胞浸润消失。18个月后治疗部位未复发。

相似文献

1
Cutaneous non-X histiocytosis: clinical and histologic features and response to dermabrasion.皮肤非X组织细胞增多症:临床与组织学特征及对皮肤磨削术的反应
J Am Acad Dermatol. 1985 Oct;13(4):645-9. doi: 10.1016/s0190-9622(85)70209-5.
2
[Hashimoto-Pritzker congenital self-healing histiocytosis].[桥本-普里茨克先天性自愈性组织细胞增多症]
Pediatrie. 1988;43(3):213-7.
3
Congenital self-healing histiocytosis (Hashimoto-Pritzker). An ultrastructural and immunohistochemical study.先天性自愈性组织细胞增多症(桥本-普利茨克病)。一项超微结构和免疫组织化学研究。
Cancer. 1988 Feb 1;61(3):508-16. doi: 10.1002/1097-0142(19880201)61:3<508::aid-cncr2820610316>3.0.co;2-2.
4
Benign non-X histiocytosis: a unique case bridging several of the non-X histiocytic syndromes.良性非X组织细胞增多症:一个连接多种非X组织细胞增多综合征的独特病例。
J Am Acad Dermatol. 1988 Jun;18(6):1282-9. doi: 10.1016/s0190-9622(88)70136-x.
5
Diffuse cutaneous reticulohistiocytosis.弥漫性皮肤网状组织细胞增生症
Arch Dermatol. 1982 Mar;118(3):173-6.
6
Regressing atypical histiocytosis. Report of a case.退行性非典型组织细胞增多症。病例报告。
Am J Dermatopathol. 1984 Jun;6(3):259-63. doi: 10.1097/00000372-198406030-00010.
7
CD1 (OKT6)-positive juvenile xanthogranuloma. OKT6 is not specific for Langerhans cell histiocytosis (histiocytosis X).
J Am Acad Dermatol. 1992 May;26(5 Pt 2):850-4. doi: 10.1016/0190-9622(92)70120-5.
8
Benign cephalic histiocytosis.良性头部组织细胞增多症
Arch Dermatol. 1986 Sep;122(9):1038-43.
9
Response of nodular non-X histiocytosis to vinblastine.
Arch Dermatol. 1982 Nov;118(11):913-7.
10
Indeterminate cell histiocytosis--a clinicopathological entity with features of both X- and non-X histiocytosis.未定型细胞组织细胞增多症——一种具有X型和非X型组织细胞增多症特征的临床病理实体。
Br J Dermatol. 1996 Mar;134(3):525-32.