• 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

[A CASE OF EOSINOPHILIC GRANULOMATOUS WITH POLYANGIITIS WITH SKIN LESIONS ASSOCIATED WITH PSORIASIS].

作者信息

Oshita Hideto, Ogata Misato, Inoue Asami, Sano Yuka, Yoshioka Koji, Ikegami Yasuhiko, Yamaoka Naoki

机构信息

Department of Respiratory Medicine, Federation of National Public Service and Affiliated Personnel Mutual Aid Associations, Yoshijima Hospital.

出版信息

Arerugi. 2023;72(5):485-489. doi: 10.15036/arerugi.72.485.

DOI:10.15036/arerugi.72.485
PMID:37460291
Abstract

A 72-year-old woman who was undergoing treatment for bronchial asthma and psoriasis vulgaris experienced malaise three months earlier and visited our hospital on account of abnormal lung shadows. Chest computed tomography revealed ground-glass opacities in the peripheral lung fields and eosinophilia in the bronchoalveolar lavage fluid, which suggested eosinophilic pneumonia. Antineutrophil cytoplasmic antibody was negative. Her lower limbs had multiple palpable papules mixed with well-treated psoriasis and the histopathology of the skin biopsy revealed eosinophil infiltration around small vessels, suggesting the occurrence of eosinophilic granulomatosis with polyangiitis (EGPA). We were able to evaluate minor skin lesions mixed with psoriasis through collaboration between the pulmonologist and the dermatologist. In the diagnosis of EGPA, it is important to carefully examine the whole body and not overlook minor findings before starting steroids.

摘要

相似文献

1
[A CASE OF EOSINOPHILIC GRANULOMATOUS WITH POLYANGIITIS WITH SKIN LESIONS ASSOCIATED WITH PSORIASIS].
Arerugi. 2023;72(5):485-489. doi: 10.15036/arerugi.72.485.
2
Torasemide-induced Vascular Purpura in the Course of Eosinophilic Granulomatosis with Polyangiitis.托拉塞米致嗜酸性肉芽肿伴多血管炎血管性紫癜。
Acta Dermatovenerol Croat. 2022 Sep;30(2):116-118.
3
Development of eosinophilic granulomatosis with polyangiitis during the clinical course of microscopic polyangiitis: A case report.显微镜下多血管炎临床病程中嗜酸性肉芽肿伴多血管炎的发展:一例报告。
Medicine (Baltimore). 2022 Nov 4;101(44):e31401. doi: 10.1097/MD.0000000000031401.
4
Eosinophilic granulomatosis with polyangiitis.嗜酸性肉芽肿伴多血管炎。
Med Clin (Barc). 2023 Apr 6;160(7):310-317. doi: 10.1016/j.medcli.2023.01.003. Epub 2023 Feb 9.
5
Negative anti-neutrophil cytoplasmic antibodies and eosinophilic granulomatosis with polyangiitis accompanied by cough variant asthma: a case report.抗中性粒细胞胞浆抗体阴性合并嗜酸性肉芽肿性多血管炎伴咳嗽变异性哮喘 1 例报告。
Ann Palliat Med. 2021 Oct;10(10):11209-11215. doi: 10.21037/apm-21-2236.
6
Eosinophilic granulomatosis with polyangiitis developed after dupilumab administration in patients with eosinophilic chronic rhinosinusitis and asthma: a case report.在患有嗜酸性慢性鼻-鼻窦炎和哮喘的患者中,使用度普利尤单抗治疗后发生嗜酸性肉芽肿伴多血管炎:病例报告。
BMC Pulm Med. 2023 Apr 19;23(1):130. doi: 10.1186/s12890-023-02415-6.
7
A rare case report of polyangiitis overlap syndrome: granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis.罕见的多血管炎重叠综合征病例报告:肉芽肿性多血管炎和嗜酸性肉芽肿性多血管炎。
BMC Pulm Med. 2018 Nov 29;18(1):181. doi: 10.1186/s12890-018-0733-2.
8
ANCA-negative eosinophilic granulomatosis with polyangiitis complicated by peripheral nerve damage: A case report.抗中性粒细胞胞浆抗体阴性的嗜酸性肉芽肿性多血管炎合并周围神经损伤:一例报告。
Medicine (Baltimore). 2023 Aug 4;102(31):e34450. doi: 10.1097/MD.0000000000034450.
9
Case Report: Middle lobe syndrome: a rare presentation in eosinophilic granulomatosis with polyangiitis.病例报告:中叶综合征:嗜酸性肉芽肿伴多血管炎的一种罕见表现。
Front Immunol. 2023 Aug 10;14:1222431. doi: 10.3389/fimmu.2023.1222431. eCollection 2023.
10
A Case of Eosinophilic Granulomatosis with Polyangiitis Presenting with Mononeuritis Multiplex.一例以多发性单神经炎为表现的嗜酸性肉芽肿伴多血管炎。
Curr Rheumatol Rev. 2022;18(4):368-372. doi: 10.2174/1573397118666220330005431.