先天性纤维脂肪瘤伴颈内静脉错构瘤改变：首次发表病例报告。

Q2 Medicine

Methodist DeBakey cardiovascular journal Pub Date : 2024-12-26 eCollection Date: 2024-01-01 DOI:10.14797/mdcvj.1519

Samer Regal, Tamer A Khafagy, Mohamed S AbdelGawad, Ehab M Saad, Ahmed A Ali

{"title":"先天性纤维脂肪瘤伴颈内静脉错构瘤改变：首次发表病例报告。","authors":"Samer Regal, Tamer A Khafagy, Mohamed S AbdelGawad, Ehab M Saad, Ahmed A Ali","doi":"10.14797/mdcvj.1519","DOIUrl":null,"url":null,"abstract":"A 25-year-old female presented with a congenital painless growing mass on the right side of her neck with symptoms of tinnitus and difficulty breathing. Imaging revealed an aneurysm of the internal jugular vein reaching a maximum diameter of 9.2 cm, shifting the trachea and right thyroid lobe to the left side. Simple excision was sufficient to treat compression symptoms and prevent potential thrombosis and embolism. This is the first reported case of aneurysmal internal jugular vein with fibrofatty degeneration and hamartomatous wall morphology associated with compression symptoms.","PeriodicalId":39207,"journal":{"name":"Methodist DeBakey cardiovascular journal","volume":"20 1","pages":"113-118"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11673465/pdf/","citationCount":"0","resultStr":"{\"title\":\"Congenital Fibrolipoma with Hamartomatous Changes of the Internal Jugular Vein: First Published Case Report.\",\"authors\":\"Samer Regal, Tamer A Khafagy, Mohamed S AbdelGawad, Ehab M Saad, Ahmed A Ali\",\"doi\":\"10.14797/mdcvj.1519\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A 25-year-old female presented with a congenital painless growing mass on the right side of her neck with symptoms of tinnitus and difficulty breathing. Imaging revealed an aneurysm of the internal jugular vein reaching a maximum diameter of 9.2 cm, shifting the trachea and right thyroid lobe to the left side. Simple excision was sufficient to treat compression symptoms and prevent potential thrombosis and embolism. This is the first reported case of aneurysmal internal jugular vein with fibrofatty degeneration and hamartomatous wall morphology associated with compression symptoms.\",\"PeriodicalId\":39207,\"journal\":{\"name\":\"Methodist DeBakey cardiovascular journal\",\"volume\":\"20 1\",\"pages\":\"113-118\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11673465/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Methodist DeBakey cardiovascular journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14797/mdcvj.1519\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methodist DeBakey cardiovascular journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14797/mdcvj.1519","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}

引用次数: 0

摘要

25岁女性，颈部右侧先天性无痛性生长肿块，伴有耳鸣和呼吸困难。影像学显示颈内静脉动脉瘤最大直径达9.2 cm，气管和右甲状腺叶向左侧移位。单纯的切除足以治疗压迫症状，防止潜在的血栓形成和栓塞。这是首次报道的动脉瘤性颈内静脉纤维脂肪变性和错构瘤壁形态与压迫症状相关的病例。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Congenital Fibrolipoma with Hamartomatous Changes of the Internal Jugular Vein: First Published Case Report.

A 25-year-old female presented with a congenital painless growing mass on the right side of her neck with symptoms of tinnitus and difficulty breathing. Imaging revealed an aneurysm of the internal jugular vein reaching a maximum diameter of 9.2 cm, shifting the trachea and right thyroid lobe to the left side. Simple excision was sufficient to treat compression symptoms and prevent potential thrombosis and embolism. This is the first reported case of aneurysmal internal jugular vein with fibrofatty degeneration and hamartomatous wall morphology associated with compression symptoms.

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

Methodist DeBakey cardiovascular journal Medicine-Medicine (all)

CiteScore

2.30

自引率

0.00%

发文量