• 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

Familial cutaneous cylindromas: investigations in five generations of a family.

作者信息

Gerretsen A L, Beemer F A, Deenstra W, Hennekam F A, van Vloten W A

机构信息

Department of Dermatology, University Hospital Utrecht, The Netherlands.

出版信息

J Am Acad Dermatol. 1995 Aug;33(2 Pt 1):199-206. doi: 10.1016/0190-9622(95)90234-1.

DOI:10.1016/0190-9622(95)90234-1
PMID:7622645
Abstract

BACKGROUND

Multiple cutaneous cylindromas are probably inherited in an autosomal dominant way.

OBJECTIVE

Our purpose was to describe a large family with cutaneous cylindromas, trichoepitheliomas, and milia occurring in five generations and to elucidate further the mode of inheritance.

METHODS

We examined 39 family members and obtained information on 31 other members from reports of relatives.

RESULTS

The pedigree included 237 members, 118 male and 119 female, with 30 affected patients (11 male, 19 female). Between 33% and 100% of the children of affected family members had one or more of these skin lesions. Female-to-female, female-to-male, male-to-female, and male-to-male inheritance occurred.

CONCLUSION

Multiple cutaneous cylindromas are inherited in an autosomal dominant way with variable clinical expression. Penetrance reaches 100% in adult life. This condition is associated with trichoepitheliomas and milia.

摘要

相似文献

1
Familial cutaneous cylindromas: investigations in five generations of a family.
J Am Acad Dermatol. 1995 Aug;33(2 Pt 1):199-206. doi: 10.1016/0190-9622(95)90234-1.
2
Brooke-Spiegler syndrome.布鲁克-施皮格勒综合征
J Eur Acad Dermatol Venereol. 2001 Jul;15(4):346-9.
3
The clinicopathological features of familial cylindromas and trichoepitheliomas (Brooke-Spiegler syndrome): a report of two families.家族性圆柱瘤和毛发上皮瘤(布鲁克-施皮格勒综合征)的临床病理特征:两个家族的报告
Clin Exp Dermatol. 1992 Sep;17(5):332-6. doi: 10.1111/j.1365-2230.1992.tb00223.x.
4
[Brooke-Spiegler syndrome].[布鲁克-施皮格勒综合征]
Ann Dermatol Venereol. 1999 Jun-Jul;126(6-7):513-7.
5
The pathogenesis of familial multiple cylindromas, trichoepitheliomas, milia, and spiradenomas.家族性多发性圆柱瘤、毛发上皮瘤、粟丘疹和汗腺螺旋腺瘤的发病机制。
Am J Dermatopathol. 1995 Jun;17(3):271-80. doi: 10.1097/00000372-199506000-00010.
6
A syndrome of trichoepitheliomas, milia, and cylindromas.毛发上皮瘤、粟丘疹和圆柱瘤综合征。
Arch Dermatol. 1975 May;111(5):610-4.
7
Familial multiple glomus tumors: report of a pedigree and literature review.家族性多发性血管球瘤:一例家系报告及文献复习
Ann Plast Surg. 1994 Jan;32(1):89-91. doi: 10.1097/00000637-199401000-00013.
8
[Brooke-Spiegler syndrome: an heterogeneous entity].布鲁克-施皮格勒综合征:一种异质性疾病
Actas Dermosifiliogr. 2006 Dec;97(10):669-72. doi: 10.1016/s0001-7310(06)73492-5.
9
A clinicopathologic and molecular biologic study of patients presenting with few adnexal tumors (two to four) from the morphological spectrum of Brooke-Spiegler syndrome.一项针对表现为布鲁克-施皮格勒综合征形态学谱中少数附件肿瘤(两到四个)患者的临床病理和分子生物学研究。
Am J Dermatopathol. 2013 Feb;35(1):19-24. doi: 10.1097/DAD.0b013e318255dd37.
10
Novel and recurrent germline and somatic mutations in a cohort of 67 patients from 48 families with Brooke-Spiegler syndrome including the phenotypic variant of multiple familial trichoepitheliomas and correlation with the histopathologic findings in 379 biopsy specimens.来自48个家庭的67例布鲁克-施皮格勒综合征患者队列中的新型和复发性种系及体细胞突变,包括多发性家族性毛发上皮瘤的表型变异,以及与379份活检标本的组织病理学结果的相关性。
Am J Dermatopathol. 2013 Feb;35(1):34-44. doi: 10.1097/DAD.0b013e31824e7658.

引用本文的文献

1
Multiple Trichoepithelioma Syndrome: A Case Report.多发性毛发上皮瘤综合征:一例报告
Cureus. 2023 Aug 4;15(8):e42930. doi: 10.7759/cureus.42930. eCollection 2023 Aug.
2
The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene.在1型多发性家族性毛发上皮瘤、布鲁克-施皮格勒综合征和家族性圆柱瘤患者中检测到的CYLD p.R758X全球复发性无义突变代表了该基因中的一个突变热点。
BMC Genet. 2016 Feb 9;17:36. doi: 10.1186/s12863-016-0346-9.
3
Malignant cylindroma in a patient with Brooke-Spiegler syndrome.
一名患有布鲁克-施皮格勒综合征患者的恶性圆柱瘤。
Dermatol Pract Concept. 2015 Apr 30;5(2):61-5. doi: 10.5826/dpc.0502a09. eCollection 2015 Apr.
4
Enucleation of cylindromas in Brooke-Spiegler syndrome: a novel surgical technique.布鲁克-施皮格勒综合征中圆柱瘤的摘除术:一种新的手术技术。
Dermatol Surg. 2014 Dec;40(12):1438-9. doi: 10.1097/DSS.0000000000000142.
5
Malignant cylindroma of the scalp arising in a setting of multiple cylindromatosis: a case report.多发性圆柱瘤病背景下发生的头皮恶性圆柱瘤:一例报告
Head Neck Pathol. 2009 Dec;3(4):315-9. doi: 10.1007/s12105-009-0138-x. Epub 2009 Sep 16.
6
Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.两个携带CYLD突变的大型多代家族中的肿瘤图谱分析:对疾病管理和肿瘤诱发的意义
Arch Dermatol. 2009 Nov;145(11):1277-84. doi: 10.1001/archdermatol.2009.262.
7
Genetics of skin appendage neoplasms and related syndromes.皮肤附属器肿瘤及相关综合征的遗传学
J Med Genet. 2005 Nov;42(11):811-9. doi: 10.1136/jmg.2004.025577.
8
Defective laminin 5 processing in cylindroma cells.圆柱瘤细胞中纤连蛋白5加工缺陷。
Am J Pathol. 2002 Feb;160(2):459-68. doi: 10.1016/S0002-9440(10)64865-1.
9
Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family.疑似结节性硬化症的家族性圆柱瘤病及在一个大家族中对圆柱瘤病基因座CYLD1的确认
J Med Genet. 1998 Oct;35(10):841-5. doi: 10.1136/jmg.35.10.841.