Pediatric Auricular Angiosarcoma: A Rare Case Report and Review of the Literature.

IF 0.7 Q4 ONCOLOGY

Case Reports in Oncology Pub Date : 2025-03-03 eCollection Date: 2025-01-01 DOI:10.1159/000543993

Ika Dewi Mayangsari, Ayu Astria Sriyana, Marlinda Adham, Harim Priyono, Aris Rahmanda, Novie Amelia Chozie, Meilania Saraswati, Indrati Suroyo

{"title":"Pediatric Auricular Angiosarcoma: A Rare Case Report and Review of the Literature.","authors":"Ika Dewi Mayangsari, Ayu Astria Sriyana, Marlinda Adham, Harim Priyono, Aris Rahmanda, Novie Amelia Chozie, Meilania Saraswati, Indrati Suroyo","doi":"10.1159/000543993","DOIUrl":null,"url":null,"abstract":"Introduction: Limited evidence exists regarding the clinical characteristics of auricular angiosarcoma in the pediatric population. To our knowledge, this represents the inaugural case report of auricular angiosarcoma in early childhood. This report aims to delineate the unique clinical features and findings associated with pediatric auricular angiosarcoma.Case presentation: We report a 7-year-old girl presented with a 2-year history of an enlarging, intermittently painful purplish-red mass in the left ear canal and undergo surgery with adjuvant chemotherapy.Conclusion: Although a rarity, auricular angiosarcoma can manifest in pediatric patients, necessitating vigilant consideration for diagnosis in this population. The evaluation and management of auricular angiosarcoma in pediatric cases demands heightened caution due to the patients' young age and the high risk of recurrence and metastases following primary treatments.","PeriodicalId":9625,"journal":{"name":"Case Reports in Oncology","volume":"18 1","pages":"429-435"},"PeriodicalIF":0.7000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11952820/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000543993","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}

引用次数: 0

Abstract

Introduction: Limited evidence exists regarding the clinical characteristics of auricular angiosarcoma in the pediatric population. To our knowledge, this represents the inaugural case report of auricular angiosarcoma in early childhood. This report aims to delineate the unique clinical features and findings associated with pediatric auricular angiosarcoma.

Case presentation: We report a 7-year-old girl presented with a 2-year history of an enlarging, intermittently painful purplish-red mass in the left ear canal and undergo surgery with adjuvant chemotherapy.

Conclusion: Although a rarity, auricular angiosarcoma can manifest in pediatric patients, necessitating vigilant consideration for diagnosis in this population. The evaluation and management of auricular angiosarcoma in pediatric cases demands heightened caution due to the patients' young age and the high risk of recurrence and metastases following primary treatments.

查看原文本刊更多论文

小儿耳廓血管肉瘤：一例罕见病例报告及文献复习。

前言：关于小儿人群中耳廓血管肉瘤的临床特征，证据有限。据我们所知，这是儿童早期耳廓血管肉瘤的首次病例报告。本报告旨在描述小儿耳廓血管肉瘤的独特临床特征和相关发现。病例介绍：我们报告一名7岁的女孩，在左耳道出现了一个扩大的、间歇性疼痛的紫红色肿块，已有2年的历史，并接受了手术和辅助化疗。结论：耳廓血管肉瘤虽然罕见，但也可在儿科患者中出现，这一人群的诊断需要警惕。由于患儿年龄小，初次治疗后复发和转移的风险高，对小儿耳廓血管肉瘤的评估和治疗需要高度谨慎。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊