• 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

[狼疮、胰岛素抵抗性糖尿病与黑棘皮病(作者译)]

[Lupus, insulin-resistant diabetes and acanthosis nigricans (author's transl)].

作者信息

Wechsler B, Michel J P, Molle D, Wechsler J, Franceschini P, Liozon F, Godeau P

出版信息

Ann Dermatol Venereol. 1981;108(1):23-30.

PMID:7235501
Abstract

The authors report the case of a 22-year-old Guatemalan in whom lupus was diagnosed 8 months after a second pregnancy. The diagnosis of lupus met the criteria of the ARA: Raynaud's syndrome, alopecia, arthralgia, thrombophlebitis, facial erythema, antinuclear factor at 1/100, Farr at 75 p. 100 and immunofluorescent demonstration of IgM binding in healthy skin. Two months after the beginning of the lupus, there was onset of insulin-resistant ketosic diabetes without overweight. The serum insulin was 1.140 mu U/ml. Acanthosis nigricans was noted and confirmed by a biopsy. Insulin-resistance can be attributed to anti-membrane receptor antibodies titrating at 1/200 (R. Khan). The short-term progress of the disease was favorable on corticosteroid treatment. Insulin could be stopped, but high insulin serum levels persisted. This case meets criteria for type B as defined by Flier, Khan and Roth, and is the first European case of lupus with a complete presentation. Short-term progress was favorable, and there is no evidence to affirm that there will be a tardive progression towards hypoglycemia which is, however, possible due to the persistence of elevated serum insulin levels.

摘要

作者报告了一例22岁危地马拉女性的病例,该患者在第二次怀孕8个月后被诊断为狼疮。狼疮的诊断符合美国风湿病学会(ARA)的标准:雷诺氏综合征、脱发、关节痛、血栓性静脉炎、面部红斑、抗核因子为1/100、Farr试验为75%、在健康皮肤中有IgM结合的免疫荧光显示。狼疮发病两个月后,出现了无超重的胰岛素抵抗性酮症糖尿病。血清胰岛素为1.140微单位/毫升。发现有黑棘皮病,并经活检证实。胰岛素抵抗可归因于抗膜受体抗体滴定度为1/200(R. Khan)。疾病的短期进展在皮质类固醇治疗下较为良好。胰岛素可以停用,但血清胰岛素水平仍持续升高。该病例符合Flier、Khan和Roth所定义的B型标准,是欧洲首例有完整表现的狼疮病例。短期进展良好,且没有证据证实会出现迟发性低血糖进展,不过,由于血清胰岛素水平持续升高,这种情况是有可能发生的。

相似文献

1
[Lupus, insulin-resistant diabetes and acanthosis nigricans (author's transl)].[狼疮、胰岛素抵抗性糖尿病与黑棘皮病(作者译)]
Ann Dermatol Venereol. 1981;108(1):23-30.
2
[Insulin resistant diabetes showing anti-insulin receptor autoantibody with systemic scleroderma, acanthosis nigricans and total lipodystrophy (author's transl)].胰岛素抵抗性糖尿病伴抗胰岛素受体自身抗体、系统性硬皮病、黑棘皮病和全身性脂肪营养不良(作者译)
Nihon Naika Gakkai Zasshi. 1980 Mar 10;69(3):361-9.
3
Insulin resistant diabetes mellitus associated with acanthosis nigricans and systemic lupus erythematosus in a Nigerian male.一名尼日利亚男性患有的与黑棘皮病和系统性红斑狼疮相关的胰岛素抵抗型糖尿病。
Afr J Med Med Sci. 1985 Mar-Jun;14(1-2):71-4.
4
[Abnormal insulin receptor type-B associated with lupus erythematosus].[与红斑狼疮相关的异常B型胰岛素受体]
Nihon Rinsho. 1983 Oct;41(10):2412-20.
5
Insulin-resistant diabetes mellitus and insulin receptor antibodies: variable association with acanthosis nigricans.胰岛素抵抗型糖尿病与胰岛素受体抗体:与黑棘皮病的可变关联。
Henry Ford Hosp Med J. 1980;28(2-3):161-7.
6
[Amenorrhea, insulin resistance and acanthosis nigricans. A hyperandrogenic and a normoandrogenic clinical forms].[闭经、胰岛素抵抗与黑棘皮症。一种高雄激素血症和一种正常雄激素血症的临床类型]
Rev Med Chil. 1993 Feb;121(2):170-5.
7
Insulin resistant diabetes mellitus without the presence of insulin antibodies. A case report.无胰岛素抗体的胰岛素抵抗型糖尿病。病例报告。
Endokrinologie. 1976 Jul;67(3):373-6.
8
Systemic lupus erythematosus with acanthosis nigricans, hyperpigmentation, and insulin receptor antibody.伴有黑棘皮病、色素沉着及胰岛素受体抗体的系统性红斑狼疮
Lupus. 1997;6(3):275-8. doi: 10.1177/096120339700600311.
9
[Insulin resistant diabetes, acanthosis nigricans and Bartter's syndrome, a fortuitous association?].[胰岛素抵抗性糖尿病、黑棘皮病与巴特综合征,一种偶然的关联?]
Arch Fr Pediatr. 1992 Apr;49(4):361-3.
10
Type B insulin resistance in a systemic lupus erythematosus patient.系统性红斑狼疮患者的 B 型胰岛素抵抗。
Int J Rheum Dis. 2009 Jul;12(2):174-6. doi: 10.1111/j.1756-185X.2009.01402.x.