<?xml version="1.0" encoding="UTF-8"?> <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd"> <ArticleSet> <Article> <Journal> <PublisherName>jmedicalcasereports</PublisherName> <JournalTitle>Frontiers in Medical Case Reports</JournalTitle> <PISSN>I</PISSN> <EISSN>S</EISSN> <Volume-Issue>Volume 5; Issue 1</Volume-Issue> <PartNumber/> <IssueTopic>Multidisciplinary</IssueTopic> <IssueLanguage>English</IssueLanguage> <Season>(Jan-Feb, 2024)</Season> <SpecialIssue>N</SpecialIssue> <SupplementaryIssue>N</SupplementaryIssue> <IssueOA>Y</IssueOA> <PubDate> <Year>-0001</Year> <Month>11</Month> <Day>30</Day> </PubDate> <ArticleType>Medical Case Reports</ArticleType> <ArticleTitle>Inguinal Arteriovenous Malformation</ArticleTitle> <SubTitle/> <ArticleLanguage>English</ArticleLanguage> <ArticleOA>Y</ArticleOA> <FirstPage>1</FirstPage> <LastPage>5</LastPage> <AuthorList> <Author> <FirstName>Abdul</FirstName> <LastName>Raheem</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>N</CorrespondingAuthor> <ORCID/> <FirstName>Syed Ali</FirstName> <LastName>Arsal</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Taha</FirstName> <LastName>Basit</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Syeda</FirstName> <LastName>Areeba</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Muhammad Salar</FirstName> <LastName>Abro</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Ashish</FirstName> <LastName>Kumar</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> </Author> </AuthorList> <DOI/> <Abstract>Arteriovenous malformations (AVMs) are rare disorders, with inguinal region involvement being particularly uncommon, as they typically manifest in the neck, limbs, trunk, and intracranial or extracranial sites. Despite their varied presentation across organs and tissues, AVMs can lead to cardiac failures due to high output, necessitating management even in asymptomatic cases. We present the case of a 37-year-old male with a known history of hypertension and severe depressive disorder, referred to the urology department for bilateral renal calculi evaluation. The patient complained of sudden-onset, moderate-intensity left-sided flank pain, with no signs of infection or constitutional symptoms. A non-contrast CT scan revealed bilateral renal calculi and an intriguing mass in the scroto-inguinal region. Further investigation through contrast-enhanced computed tomography identified an AVM originating from the right internal iliac artery, located a few millimeters next to the scrotum. A multidisciplinary team, including interventional radiology, urology, and vascular surgery, collaborated to develop a curative strategy. Angioembolization was performed successfully in a single session, involving catheterization and ligation of the feeder vessel using a lipiodol-glue mixture. Postoperatively, the patient remained stable with mild pyrexia (99__degreesignF), a heart rate of 76 bpm, and blood pressure fluctuating between 110-125 mmHg systolic and 72-80 mmHg diastolic. The absence of glue leakage upon saline injection confirmed the effectiveness of embolization. The patient experienced relief from pain and was mobilized on the second postoperative day. This case underscores the importance of a comprehensive approach in managing rare presentations of AVMs, emphasizing successful angioembolization as a viable therapeutic option.</Abstract> <AbstractLanguage>English</AbstractLanguage> <Keywords>Arteriovenous Malformation,Inguinal Avm,Embolotherapy,Computed Tomography Angiography</Keywords> <URLs> <Abstract>https://jmedicalcasereports.org/ubijournal-v1copy/journals/abstract.php?article_id=15017&title=Inguinal Arteriovenous Malformation</Abstract> </URLs> <References> <ReferencesarticleTitle>References</ReferencesarticleTitle> <ReferencesfirstPage>16</ReferencesfirstPage> <ReferenceslastPage>19</ReferenceslastPage> <References>Greene AK, Orbach DB. Management of arteriovenous malformations. Clin Plast Surg 2011; 38: 95-106. Igari K, Kudo T, Toyofuku T, Jibiki M, Inoue Y. Surgical Treatment with or without Embolotherapy for Arteriovenous Malformations. Ann Vasc Dis 2013; 6: 46-51. Maddy K, Chalamgari A, Ariwodo O, Nisseau-Bey Z, Maldonado J, Lucke-Wold B. An updated review on the genetics of arteriovenous malformations. Gene Protein Dis 2023; 2: 0312. Nakabayashi R, Matsubara T, Shimada G. Arteriovenous malformation of the spermatic cord mimicking reducible inguinal hernia. Asian J Endosc Surg 2023; 16: 575-578. Nakabayashi R, Matsubara T, Shimada G. Arteriovenous malformation of the spermatic cord mimicking reducible inguinal hernia. Asian J Endosc Surg 2023; 16: 575-578. Nazari I, Zargar MA, Panahi P, Alavi SMA. Pelvic arteriovenous malformation (AVM) with recurrent hematuria: A case report. Int J Surg Case Rep 2023; 110: 108701. Schimmel K, Ali MK, Tan SY, Teng J, Do HM, Steinberg GK, Stevenson DA, Spiekerkoetter E. Arteriovenous Malformations-Current Understanding of the Pathogenesis with Implications for Treatment. Int J Mol Sci 2021; 22: 9037. Sountoulides P, Bantis A, Asouhidou I, Aggelonidou H. Arteriovenous malformation of the spermatic cord as the cause of acute scrotal pain: a case report. J Med Case Rep 2007; 1: 110. Tseng WK, Su IC, Chen MT, Lee JJ. Spontaneous Regression of Parapharyngeal Arteriovenous Malformation. Vasc Endovascular Surg 2018; 52: 313-315. Yakes WF. Endovascular management of high-flow arteriovenous malformations. Semin Intervent Radiol 2004; 21: 49-58.</References> </References> </Journal> </Article> </ArticleSet>