• 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

与蕈样肉芽肿预后和慢性化相关的临床病理因素:一项回顾性队列研究。

Clinicopathological Factors Associated with the Prognosis and Chronicity of Lymphomatoid Papulosis: A Retrospective Cohort Study.

机构信息

Department of Dermatology, Asan Medical Center, University of Ulsan College of Medicine, 88, Songpa-gu, Seoul, Korea.

Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, 88, Songpa-gu, Seoul, Korea.

出版信息

Clin Lymphoma Myeloma Leuk. 2022 Jul;22(7):e541-e548. doi: 10.1016/j.clml.2022.02.004. Epub 2022 Feb 24.

DOI:10.1016/j.clml.2022.02.004
PMID:35307318
Abstract

BACKGROUND

The clinical and pathological features of lymphomatoid papulosis (LYP) are diverse. The objective of this study is to evaluate the clinical and pathological features associated with the prognosis and clinical course of LYP.

PATIENTS AND METHODS

The clinical and pathological features of LYP in a medical center database were retrospectively retrieved.

RESULTS

Overall, 58 LYP patients were included in the study. The mean age at diagnosis was 39.1 years and the female-to-male ratio was 1:1.2. More than two-thirds (40/58, 69.0%) of the patients showed a chronic and recurrent disease course. A longer pre-diagnosis duration (odds ratio (OR), 1.01; 95% confidence interval (CI), 1.00-1.03) was significantly associated with secondary lymphoma development. Lower extremity involvement (OR, 10.40; 95% CI, 1.17-92.28) and the absence of eosinophils in the lesions (OR, 11.28; 95% CI, 1.01-126.24) were found to be significantly associated with the chronic and recurrent course of LYP.

CONCLUSION

A longer pre-diagnosis duration is associated with secondary lymphoma, while a lower extremity involvement and the absence of lesional eosinophil infiltration are associated with the chronicity of LYP.

摘要

背景

蕈样肉芽肿(LYP)的临床表现和病理特征多种多样。本研究旨在评估与 LYP 预后和临床病程相关的临床和病理特征。

患者与方法

本研究通过回顾性检索医疗中心数据库中 LYP 的临床和病理特征。

结果

总体而言,本研究纳入了 58 例 LYP 患者。诊断时的平均年龄为 39.1 岁,男女比例为 1:1.2。超过三分之二(40/58,69.0%)的患者表现为慢性和复发性疾病过程。较长的预诊断时间(比值比(OR),1.01;95%置信区间(CI),1.00-1.03)与继发性淋巴瘤的发生显著相关。下肢受累(OR,10.40;95%CI,1.17-92.28)和病变中无嗜酸性粒细胞浸润(OR,11.28;95%CI,1.01-126.24)与 LYP 的慢性和复发性病程显著相关。

结论

较长的预诊断时间与继发性淋巴瘤相关,而下肢受累和病变中无嗜酸性粒细胞浸润与 LYP 的慢性病程相关。

相似文献

1
Clinicopathological Factors Associated with the Prognosis and Chronicity of Lymphomatoid Papulosis: A Retrospective Cohort Study.与蕈样肉芽肿预后和慢性化相关的临床病理因素:一项回顾性队列研究。
Clin Lymphoma Myeloma Leuk. 2022 Jul;22(7):e541-e548. doi: 10.1016/j.clml.2022.02.004. Epub 2022 Feb 24.
2
Frequency and Risk Factors for Associated Lymphomas in Patients With Lymphomatoid Papulosis.淋巴瘤样丘疹病患者相关淋巴瘤的发生率及危险因素
Oncologist. 2016 Jan;21(1):76-83. doi: 10.1634/theoncologist.2015-0242. Epub 2015 Dec 14.
3
Paediatric-onset lymphomatoid papulosis: results of a multicentre retrospective cohort study on behalf of the EORTC Cutaneous Lymphoma Tumours Group (CLTG).儿童发病的蕈样肉芽肿病:EORTC 皮肤淋巴瘤肿瘤学组(CLTG)代表进行的一项多中心回顾性队列研究结果。
Br J Dermatol. 2024 Jul 16;191(2):233-242. doi: 10.1093/bjd/ljae150.
4
Localized lymphomatoid papulosis: Unilesional lymphomatoid papulosis, regional lymphomatoid papulosis, and persistent agmination of lymphomatoid papulosis.局限性蕈样肉芽肿病:单发性蕈样肉芽肿病、区域性蕈样肉芽肿病和蕈样肉芽肿病持续聚集。
Clin Dermatol. 2022 Nov-Dec;40(6):622-638. doi: 10.1016/j.clindermatol.2022.07.010. Epub 2022 Jul 28.
5
Lymphomatoid papulosis: Treatment response and associated lymphomas in a study of 180 patients.蕈样肉芽肿病:180 例患者研究中的治疗反应和相关淋巴瘤。
J Am Acad Dermatol. 2016 Jan;74(1):59-67. doi: 10.1016/j.jaad.2015.09.013. Epub 2015 Oct 28.
6
Evaluation of Associated Lymphomas and Their Risk Factors in Patients with Lymphomatoid Papulosis: A Retrospective Single-Center Study from Turkey.评价土耳其单中心回顾性研究中蕈样肉芽肿患者伴发淋巴瘤及其危险因素。
Turk J Haematol. 2021 Feb 25;38(1):49-56. doi: 10.4274/tjh.galenos.2020.2020.0685. Epub 2021 Jan 4.
7
Acral lymphomatoid papulosis: Report of five cases, differential diagnosis, and review.肢端淋巴组织增生性蕈样肉芽肿:五例报告、鉴别诊断及复习。
J Cutan Pathol. 2021 May;48(5):650-658. doi: 10.1111/cup.13929. Epub 2021 Jan 13.
8
Histopathological aspects and differential diagnosis of CD8 positive lymphomatoid papulosis.CD8阳性淋巴瘤样丘疹病的组织病理学特征及鉴别诊断
J Cutan Pathol. 2016 Nov;43(11):963-973. doi: 10.1111/cup.12779. Epub 2016 Aug 30.
9
[Lymphomatoid papulosis in a 2 1/2-year-old boy].[一名2岁半男童的淋巴瘤样丘疹病]
Hautarzt. 2011 Nov;62(11):807-9. doi: 10.1007/s00105-011-2245-3.
10
Lymphomatoid papulosis: is a second lymphoma commoner among East Asians?蕈样肉芽肿:是东亚人中更为常见的第二种淋巴瘤吗?
Clin Exp Dermatol. 2012 Mar;37(2):118-21. doi: 10.1111/j.1365-2230.2011.04124.x. Epub 2011 Jul 25.

引用本文的文献

1
Primary Cutaneous CD30+ Lymphoproliferative Disorders in South Korea: A Nationwide, Multi-Center, Retrospective, Clinical, and Prognostic Study.韩国原发性皮肤CD30+淋巴增殖性疾病:一项全国性、多中心、回顾性、临床及预后研究
Ann Dermatol. 2025 Apr;37(2):75-85. doi: 10.5021/ad.24.120.