首页> 外文期刊>Case Reports in Dermatological Medicine >Granuloma Multiforme: A Rare Granulomatous Disease
【24h】

Granuloma Multiforme: A Rare Granulomatous Disease

机译:肉芽肿多形状:罕见的肉芽肿病

获取原文
           

摘要

Granuloma Multiforme (GM) is a reactive skin disorder with annular lesion and focal necrobiosis. It was first described in Nigeria (Africa), since than it was mostly described from various regions of Africa where leprosy was endemic. Outside Africa, this disease is rarely reported. Till 2016 only five cases were reported from India. This is the second case report from Nepal. A fifty-nine-year-old female, farmer by occupation, presented with annular and polycyclic plaques with elevated beaded border for one year. It was distributed over upper trunk, lower back, and arms, and was mildly pruritic. Histopathologically, loss of elastic fibres at focal area of upper dermis, with elastic fibres engulfed histiocytes were noted. GM was mostly noted from leprosy endemic areas of Africa. Clinically, it is very difficult to distinguish from granuloma annulare. This report adds the number of GM occurrence in Asia especially from area where leprosy is still prevalent. This report also emphasizes in resource poor settings where most diagnosis is made clinically, the granuloma annulare should be looked for very carefully in order not to miss GM.
机译:肉芽肿多形态(GM)是一种具有环状病变和焦点症状的活性皮肤病。它首先在尼日利亚(非洲)描述,因为它大多是从非洲的各个地区描述的,其中麻风病是地方性的。非洲以外,这种疾病很少报道。直到2016年,印度只报告了五起案件。这是尼泊尔的第二个案例报告。一位五十九岁的女性,农民通过职业,用环形和多环斑块呈现,凸起边界升高一年。它分布在上躯干,下背部和臂上,温和的瘙痒。组织病理学上,注意到上皮丝焦点的弹性纤维的丧失,并注意到具有弹性纤维吞噬的组织细胞。 GM大多是从非洲的麻风病地区注意到的。临床上,很难区分肉芽肿。本报告增加了亚洲的转基因发生的数量,特别是从麻风病仍然普遍的区域。本报告还强调资源较差的环境,其中大多数诊断在临床上进行,应当谨慎地仔细寻找肉芽肿的载载,以免Mis。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号