• 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

一例帕西尼和皮耶里尼特发性皮肤萎缩临床病例并文献复习

A Clinical Case of Idiopathic Atrophoderma of Pasini and Pierini With Literature Review.

作者信息

Pathak Raksha, Neupane Poshan, Shrestha Samir

机构信息

Department of Dermatology and Venereology, Gandaki Medical College, Pokhara, Nepal.

Department of Medicine, Nepal Mediciti Hospital, Lalitpur, Nepal.

出版信息

Case Rep Dermatol Med. 2025 Mar 14;2025:8886954. doi: 10.1155/crdm/8886954. eCollection 2025.

DOI:10.1155/crdm/8886954
PMID:40123740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11928212/
Abstract

Atrophoderma of Pasini and Pierini is a rare skin disease that presents with dermal atrophy. Differentiating this condition from morphea remains a challenge. Etiology is unknown, and there is no effective treatment till date. The diagnosis is made through clinicohistopathological correlation.

摘要

帕西尼和皮耶里尼皮肤萎缩症是一种罕见的皮肤病，表现为皮肤萎缩。将这种病症与硬斑病区分开来仍然是一项挑战。病因不明，迄今为止尚无有效的治疗方法。通过临床组织病理学相关性进行诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/b3924ab46ddf/CRIDM2025-8886954.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/b1a96be2f70c/CRIDM2025-8886954.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/8bc6696ba119/CRIDM2025-8886954.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/533103194214/CRIDM2025-8886954.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/b3924ab46ddf/CRIDM2025-8886954.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/b1a96be2f70c/CRIDM2025-8886954.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/8bc6696ba119/CRIDM2025-8886954.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/533103194214/CRIDM2025-8886954.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c2/11928212/b3924ab46ddf/CRIDM2025-8886954.004.jpg

相似文献

1
A Clinical Case of Idiopathic Atrophoderma of Pasini and Pierini With Literature Review.一例帕西尼和皮耶里尼特发性皮肤萎缩临床病例并文献复习
Case Rep Dermatol Med. 2025 Mar 14;2025:8886954. doi: 10.1155/crdm/8886954. eCollection 2025.
2
BULGARIAN PATIENT WITH ATROPHODERMA OF PASINI AND PIERINI- DESCRIPTION OF A CASE AND SHORT UPDATE.一名患有帕西尼和皮耶里尼萎缩性皮病的保加利亚患者——病例描述及简要进展
Georgian Med News. 2023 Jul-Aug(340-341):227-231.
3
Idiopathic Atrophoderma of Pasini and Pierini: A Case Report and Literature Review.帕西尼和皮耶里尼特发性皮肤萎缩：病例报告及文献综述
Cureus. 2022 Jul 5;14(7):e26571. doi: 10.7759/cureus.26571. eCollection 2022 Jul.
4
Idiopathic Atrophoderma of Pasini and Pierini: Response to Mycophenolic Acid Treatment.帕西尼和皮耶里尼特发性皮肤萎缩：对霉酚酸治疗的反应。
Cureus. 2025 Jan 14;17(1):e77439. doi: 10.7759/cureus.77439. eCollection 2025 Jan.
5
Idiopathic Atrophoderma of Pasini and Pierini: Case report and literature review.帕西尼和皮耶里尼特发性萎缩性皮病：病例报告及文献综述
Clin Case Rep. 2018 Dec 18;7(2):258-263. doi: 10.1002/ccr3.1958. eCollection 2019 Feb.
6
Congenital idiopathic atrophoderma of Pasini and Pierini.帕西尼和皮耶里尼先天性特发性皮肤萎缩
Dermatol Online J. 2012 Apr 15;18(4):4.
7
Congenital atrophoderma of Pasini and Pierini.帕西尼和皮耶里尼先天性萎缩性皮病
J Korean Med Sci. 2006 Feb;21(1):169-71. doi: 10.3346/jkms.2006.21.1.169.
8
Atrophoderma of Pasini and Pierini. An immunopathologic case study.帕西尼和皮耶里尼皮肤萎缩症。一项免疫病理学病例研究。
Am J Clin Pathol. 1992 Jan;97(1):63-8. doi: 10.1093/ajcp/97.1.63.
9
Concomitant unilateral idiopathic atrophoderma of Pasini and Pierini (IAPP) and morphea. Observations supporting IAPP as a variant of morphea.伴发单侧帕西尼和皮耶里尼特发性萎缩性皮病（IAPP）与硬斑病。支持IAPP作为硬斑病一种变体的观察结果。
Int J Dermatol. 1990 May;29(4):281-3. doi: 10.1111/j.1365-4362.1990.tb02562.x.
10
Progressive idiopathic atrophoderma of Pasini and Pierini.帕西尼和皮耶里尼进行性特发性皮肤萎缩
Cutis. 1980 May;25(5):503-6.

引用本文的文献

1
Comparative Analysis of Large Language Models in Dermatological Diagnosis: An Evaluation of Diagnostic Accuracy.大语言模型在皮肤病诊断中的比较分析：诊断准确性评估
Cureus. 2025 Sep 11;17(9):e92089. doi: 10.7759/cureus.92089. eCollection 2025 Sep.

本文引用的文献

1
Idiopathic Atrophoderma of Pasini and Pierini: A Case Report and Literature Review.帕西尼和皮耶里尼特发性皮肤萎缩：病例报告及文献综述
Cureus. 2022 Jul 5;14(7):e26571. doi: 10.7759/cureus.26571. eCollection 2022 Jul.
2
Idiopathic Atrophoderma of Pasini and Pierini: Case report and literature review.帕西尼和皮耶里尼特发性萎缩性皮病：病例报告及文献综述
Clin Case Rep. 2018 Dec 18;7(2):258-263. doi: 10.1002/ccr3.1958. eCollection 2019 Feb.
3
Idiopathic atrophoderma of Pasini and Pierini: A case study of collagen and elastin texture by multiphoton microscopy.
特发性帕西尼-皮耶里尼皮肤萎缩症：多光子显微镜下胶原和弹力蛋白纹理的病例研究。
J Am Acad Dermatol. 2017 Nov;77(5):930-937. doi: 10.1016/j.jaad.2017.02.044. Epub 2017 Apr 25.
4
Atrophoderma of Pasini and Pierini in a blaschkoid pattern.呈线状痣样条纹状的帕西尼和皮耶里尼皮肤萎缩症。
J Dtsch Dermatol Ges. 2017 Jun;15(6):663-664. doi: 10.1111/ddg.13198. Epub 2017 Mar 27.
5
Atrophoderma of Pasini and Pierini associated with extramedullary plasmacytoma.帕西尼和皮耶里尼萎缩性皮病伴发髓外浆细胞瘤
Clin Exp Dermatol. 2016 Oct;41(7):837-9. doi: 10.1111/ced.12906. Epub 2016 Jul 22.
6
Idiopathic congenital atrophoderma of Pasini and Pierini.帕西尼和皮耶里尼特发性先天性萎缩性皮病
Arch Dis Child. 2015 Dec;100(12):1184. doi: 10.1136/archdischild-2015-309498. Epub 2015 Sep 15.
7
Congenital idiopathic atrophoderma of Pasini and Pierini.帕西尼和皮耶里尼先天性特发性皮肤萎缩
Int J Dermatol. 2015 Jan;54(1):e44-6. doi: 10.1111/ijd.12597. Epub 2014 Oct 14.
8
Congenital idiopathic atrophoderma of Pasini and Pierini.帕西尼和皮耶里尼先天性特发性皮肤萎缩
Dermatol Online J. 2012 Apr 15;18(4):4.
9
A Case of Atrophoderma of Pasini and Pierini Associated with Borrelia burgdorferi Infection Successfully Treated with Oral Doxycycline.一例与伯氏疏螺旋体感染相关的帕西尼和皮耶里尼皮肤萎缩症，口服多西环素治疗成功
Ann Dermatol. 2011 Aug;23(3):352-6. doi: 10.5021/ad.2011.23.3.352. Epub 2011 Aug 6.
10
Exacerbated course of atrophoderma of Pasini and Pierini in patient with papillary cancer of the thyroid gland.甲状腺乳头状癌患者伴发的帕西尼和皮耶里尼萎缩性皮病的病情加重过程。
Wiad Lek. 2010;63(1):24-6.