• 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

混合性血管痣(皮肤血管性孪生痣)伴两例 Dyke-Davidoff-Masson 型颅内血管畸形。

Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients.

机构信息

Chair of Pediatrics, Department of Educational Sciences, University of Catania, Catania, Italy.

出版信息

Am J Med Genet A. 2012 Nov;158A(11):2870-80. doi: 10.1002/ajmg.a.35221. Epub 2012 Sep 18.

DOI:10.1002/ajmg.a.35221
PMID:22991195
Abstract

The term twin spotting refers to phenotypes characterized by the spatial and temporal co-occurrence of two (or more) different nevi arranged in variable cutaneous patterns, and can be associated with extra-cutaneous anomalies. Several examples of twin spotting have been described in humans including nevus vascularis mixtus, cutis tricolor, lesions of overgrowth, and deficient growth in Proteus and Elattoproteus syndromes, epidermolytic hyperkeratosis of Brocq, and the so-called phacomatoses pigmentovascularis and pigmentokeratotica. We report on a 28-year-old man and a 15-year-old girl, who presented with a previously unrecognized association of paired cutaneous vascular nevi of the telangiectaticus and anemicus types (naevus vascularis mixtus) distributed in a mosaic pattern on the face (in both patients) and over the entire body (in the man) and a complex brain malformation (in both patients) consisting of cerebral hemiatrophy, hypoplasia of the cerebral vessels and homolateral hypertrophy of the skull and sinuses (known as Dyke-Davidoff-Masson malformation). Both patients had facial asymmetry and the young man had facial dysmorphism, seizures with EEG anomalies, hemiplegia, insulin-dependent diabetes mellitus (IDDM), autoimmune thyroiditis, a large hepatic cavernous vascular malformation, and left Legg-Calvé-Perthes disease (LCPD) [LCPD-like presentation]. Array-CGH analysis and mutation analysis of the RASA1 gene were normal in both patients.

摘要

双斑(twin spotting)一词是指两种(或更多)不同痣在空间和时间上同时出现,并以不同的皮肤模式排列的表型,可伴有皮肤外异常。在人类中已经描述了几种双斑的例子,包括混合性血管痣、三色痣、过度生长病变和 Proteus 和 Elattoproteus 综合征中的生长不良、Brocq 表皮松解性角化过度症,以及所谓的色素血管性和色素角化性 phacomatoses。我们报告了一名 28 岁男性和一名 15 岁女孩,他们以前未被识别的关联是伴有毛细血管扩张型和贫血型(混合性血管痣)的成对皮肤血管痣,呈镶嵌模式分布在面部(在两名患者中)和全身(在男性中),以及复杂的脑畸形(在两名患者中),包括大脑偏侧萎缩、脑血管发育不良和同侧颅骨和窦肥大(称为 Dyke-Davidoff-Masson 畸形)。两名患者均有面部不对称,年轻男性有面部畸形、EEG 异常的癫痫、偏瘫、胰岛素依赖型糖尿病(IDDM)、自身免疫性甲状腺炎、大的肝海绵状血管畸形和左侧 Legg-Calvé-Perthes 病(LCPD)[LCPD 样表现]。在两名患者中,阵列-CGH 分析和 RASA1 基因突变分析均正常。

相似文献

1
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients.混合性血管痣(皮肤血管性孪生痣)伴两例 Dyke-Davidoff-Masson 型颅内血管畸形。
Am J Med Genet A. 2012 Nov;158A(11):2870-80. doi: 10.1002/ajmg.a.35221. Epub 2012 Sep 18.
2
Mixed vascular nevus syndrome: a report of four new cases and a literature review.混合性血管痣综合征:4例新病例报告及文献复习
Quant Imaging Med Surg. 2016 Oct;6(5):515-524. doi: 10.21037/qims.2016.10.09.
3
Hereditary neurocutaneous angiomatosis. Report of four cases.
J Neurosurg. 1996 Dec;85(6):1135-42. doi: 10.3171/jns.1996.85.6.1135.
4
Naevus vascularis mixtus and mixed vascular naevus syndrome.混合性血管痣和混合性血管痣综合征。
Clin Exp Dermatol. 2021 Jan;46(1):34-41. doi: 10.1111/ced.14369. Epub 2020 Aug 26.
5
Facial capillary malformation and Dyke-Davidoff-Masson syndrome.面部毛细管畸形和 Dyke-Davidoff-Masson 综合征。
Pediatr Neurol. 2010 Sep;43(3):202-4. doi: 10.1016/j.pediatrneurol.2010.04.011.
6
[Syndromes with vascular skin anomalies].[伴有血管性皮肤异常的综合征]
Hautarzt. 2019 Jul;70(7):474-480. doi: 10.1007/s00105-019-4418-4.
7
Dyke-Davidoff-Masson syndrome: A rare cause of cerebral hemiatrophy in children.戴克-戴维多夫-马森综合征:儿童大脑半球萎缩的罕见病因。
J Pediatr Neurosci. 2016 Jul-Sep;11(3):252-254. doi: 10.4103/1817-1745.193365.
8
Dyke-Davidoff-Masson syndrome.戴克-戴维多夫-马森综合征
Indian Pediatr. 2008 Nov;45(11):927-8.
9
Corpus callosum arteriovenous malformation with persistent trigeminal artery.伴有持续性三叉动脉的胼胝体动静脉畸形
Br J Neurosurg. 2011 Dec;25(6):736-40. doi: 10.3109/02688697.2011.554583. Epub 2011 Apr 18.
10
DYKE-DAVIDOFF-MASSON SYNDROME-A Rare Cause of Cerebral Hemiatrophy in a 17-Years-Old Ethiopian Patient: A Case Report.戴克-大卫多夫-马森综合征——一名17岁埃塞俄比亚患者脑半球萎缩的罕见病因:病例报告
Ethiop J Health Sci. 2019 Mar;29(2):287-290. doi: 10.4314/ejhs.v29i2.16.

引用本文的文献

1
A six-attribute classification of genetic mosaicism.六种属性的遗传嵌合体分类。
Genet Med. 2020 Nov;22(11):1743-1757. doi: 10.1038/s41436-020-0877-3. Epub 2020 Jul 14.
2
[Syndromes with vascular skin anomalies].[伴有血管性皮肤异常的综合征]
Hautarzt. 2019 Jul;70(7):474-480. doi: 10.1007/s00105-019-4418-4.
3
Mixed vascular nevus syndrome: a report of four new cases and a literature review.混合性血管痣综合征:4例新病例报告及文献复习
Quant Imaging Med Surg. 2016 Oct;6(5):515-524. doi: 10.21037/qims.2016.10.09.
4
Stickler syndrome associated with epilepsy: report of three cases.与癫痫相关的斯蒂克勒综合征:三例报告。
Eur J Pediatr. 2015 May;174(5):697-701. doi: 10.1007/s00431-015-2514-8. Epub 2015 Mar 27.
5
Dyke-davidoff-masson syndrome: cases of two brothers and literature review.戴克-戴维多夫-马森综合征:两兄弟的病例及文献综述
J Epilepsy Res. 2014 Jun 30;4(1):24-7. doi: 10.14581/jer.14006. eCollection 2014 Jun.
6
[How frequently does genetic mosaicism occur in the skin?].[皮肤中基因镶嵌现象的发生频率如何?]
Hautarzt. 2014 Jun;65(6):536-41. doi: 10.1007/s00105-013-2716-9.