粘膜血管平滑肌瘤：对诊断有价值的粘膜镜检查结果。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2025-02-24 DOI:10.1136/bcr-2024-262999

Harry Fruchtman, Danielle Peterson, Scott Diamond, Bijan Safai

{"title":"粘膜血管平滑肌瘤：对诊断有价值的粘膜镜检查结果。","authors":"Harry Fruchtman, Danielle Peterson, Scott Diamond, Bijan Safai","doi":"10.1136/bcr-2024-262999","DOIUrl":null,"url":null,"abstract":"This article presents a female patient in her 40s who presented with a tender violaceous bump on her upper right lip. Our primary differential diagnosis was an arteriovenous malformation. Punch biopsy revealed the lesion to be an angioleiomyoma (ALM). The punch biopsy was sufficient for the complete removal of the lesion, and the lesion did not recur to date. There were no complications. We discuss the dermatoscopic description of an ALM and its clinical picture.","PeriodicalId":9080,"journal":{"name":"BMJ Case Reports","volume":"18 2","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2025-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mucosal angioleiomyoma: mucoscopic findings adding value to diagnosis.\",\"authors\":\"Harry Fruchtman, Danielle Peterson, Scott Diamond, Bijan Safai\",\"doi\":\"10.1136/bcr-2024-262999\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This article presents a female patient in her 40s who presented with a tender violaceous bump on her upper right lip. Our primary differential diagnosis was an arteriovenous malformation. Punch biopsy revealed the lesion to be an angioleiomyoma (ALM). The punch biopsy was sufficient for the complete removal of the lesion, and the lesion did not recur to date. There were no complications. We discuss the dermatoscopic description of an ALM and its clinical picture.\",\"PeriodicalId\":9080,\"journal\":{\"name\":\"BMJ Case Reports\",\"volume\":\"18 2\",\"pages\":\"\"},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2025-02-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMJ Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1136/bcr-2024-262999\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMJ Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/bcr-2024-262999","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}

引用次数: 0

摘要

这篇文章介绍了一位40多岁的女性患者，她的右上唇出现了一个柔软的紫色肿块。我们最初的鉴别诊断是动静脉畸形。穿刺活检显示病变为血管平滑肌瘤（ALM）。穿孔活检足以完全切除病变，病变至今未复发。没有并发症。我们讨论皮肤镜描述的一个ALM和它的临床图片。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文

微信好友朋友圈 QQ好友复制链接

本刊更多论文

Mucosal angioleiomyoma: mucoscopic findings adding value to diagnosis.

This article presents a female patient in her 40s who presented with a tender violaceous bump on her upper right lip. Our primary differential diagnosis was an arteriovenous malformation. Punch biopsy revealed the lesion to be an angioleiomyoma (ALM). The punch biopsy was sufficient for the complete removal of the lesion, and the lesion did not recur to date. There were no complications. We discuss the dermatoscopic description of an ALM and its clinical picture.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

BMJ Case Reports Medicine-Medicine (all)

CiteScore

1.40

自引率

0.00%

发文量

1588

期刊介绍： BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.