• 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

退行性非典型组织细胞增多症。异常原胸腺细胞分化、T细胞受体基因重排及淋巴结受累。

Regressing atypical histiocytosis. Aberrant prothymocyte differentiation, T-cell receptor gene rearrangements, and nodal involvement.

作者信息

Jaworsky C, Cirillo-Hyland V, Petrozzi J W, Lessin S R, Murphy G F

机构信息

Department of Dermatology, University of Pennsylvania, Philadelphia 19104.

出版信息

Arch Dermatol. 1990 Dec;126(12):1609-16. doi: 10.1001/archderm.126.12.1609.

DOI:10.1001/archderm.126.12.1609
PMID:1701620
Abstract

Two cases of regressing atypical histiocytosis were studied. New findings reported include the presence of CD1 epitope on large atypical histiocytoid cells and apparent early lymph node involvement. Because regressing atypical histiocytosis may demonstrate aberrant thymic differentiation antigen expression and T-cell receptor gene rearrangements, initial lymph node involvement, and eventuation in conventional lymphoma in some cases, the alternative term regressing-phase anaplastic lymphoma is proposed as a more accurate designation for this entity.

摘要

对两例消退性非典型组织细胞增多症进行了研究。报告的新发现包括在大型非典型组织细胞样细胞上存在CD1表位以及明显的早期淋巴结受累。由于消退性非典型组织细胞增多症可能表现出异常的胸腺分化抗原表达和T细胞受体基因重排、初始淋巴结受累,且在某些情况下最终发展为传统淋巴瘤,因此建议使用替代术语“消退期间变性淋巴瘤”来更准确地命名这一实体。

相似文献

1
Regressing atypical histiocytosis. Aberrant prothymocyte differentiation, T-cell receptor gene rearrangements, and nodal involvement.退行性非典型组织细胞增多症。异常原胸腺细胞分化、T细胞受体基因重排及淋巴结受累。
Arch Dermatol. 1990 Dec;126(12):1609-16. doi: 10.1001/archderm.126.12.1609.
2
Regressing atypical histiocytosis, a regressing cutaneous phase of Ki-1-positive anaplastic large cell lymphoma. Immunocytochemical, nucleic acid, and cytogenetic studies of a new case in view of current opinion.消退性非典型组织细胞增多症,即Ki-1阳性间变性大细胞淋巴瘤的消退性皮肤期。鉴于当前观点,对一例新病例进行免疫细胞化学、核酸和细胞遗传学研究。
Cancer. 1992 Jul 15;70(2):476-83. doi: 10.1002/1097-0142(19920715)70:2<476::aid-cncr2820700216>3.0.co;2-5.
3
Primary anaplastic large-cell lymphoma of the skin. A case report suggesting that regressing atypical histiocytosis and lymphomatoid papulosis are subsets.原发性皮肤间变性大细胞淋巴瘤。一例病例报告提示消退性非典型组织细胞增多症和淋巴瘤样丘疹病是其亚型。
J Am Acad Dermatol. 1994 Feb;30(2 Pt 2):358-63. doi: 10.1016/s0190-9622(94)70040-0.
4
Self-regressing S100-negative CD1a-positive cutaneous histiocytosis.
Am J Dermatopathol. 2013 Jun;35(4):e57-9. doi: 10.1097/DAD.0b013e31827adc72.
5
Lineage differentiation of canine lymphoma/leukemias and aberrant expression of CD molecules.犬淋巴瘤/白血病的谱系分化及CD分子的异常表达
Vet Immunol Immunopathol. 2005 Jul 15;106(3-4):179-96. doi: 10.1016/j.vetimm.2005.02.020.
6
Primary and secondary cutaneous Ki-1+ (CD30+) anaplastic large cell lymphomas. Morphologic, immunohistologic, and clinical-characteristics.原发性和继发性皮肤Ki-1+(CD30+)间变性大细胞淋巴瘤。形态学、免疫组织学及临床特征
Am J Pathol. 1989 Aug;135(2):359-67.
7
Regressing atypical histiocytosis and lymphomatoid papulosis: variants of the same disorder?
Br J Dermatol. 1990 Oct;123(4):515-21. doi: 10.1111/j.1365-2133.1990.tb01458.x.
8
Double immunostaining with CD1A and CD68 in the phenotypic characterization of indeterminate cell histiocytosis.在不确定细胞组织细胞增多症的表型特征分析中使用CD1A和CD68进行双重免疫染色。
Cesk Patol. 2008 Apr;44(2):37-9.
9
Immunohistochemical expression of Langerin in Langerhans cell histiocytosis and non-Langerhans cell histiocytic disorders.朗格汉斯细胞组织细胞增多症和非朗格汉斯细胞组织细胞增生性疾病中Langerin的免疫组化表达
Am J Surg Pathol. 2008 Apr;32(4):615-9. doi: 10.1097/PAS.0b013e31815b212b.
10
Large-cell anaplastic (Ki-1-positive) lymphoma complicated by disseminated intravascular coagulation.大细胞间变性(Ki-1阳性)淋巴瘤合并弥散性血管内凝血。
Arch Pathol Lab Med. 1991 Feb;115(2):188-92.

引用本文的文献

1
Ki-1 positive anaplastic large cell lymphoma of skin.皮肤Ki-1阳性间变性大细胞淋巴瘤
J Clin Pathol. 1991 Jul;44(7):614. doi: 10.1136/jcp.44.7.614-a.