{"title":"动静脉畸形破裂血管内鱿鱼栓塞术后的胼胝体肉芽肿。","authors":"Linford Fernandes, Fathallah Ismail Islim, Fozia Saeed, Tufail Patankar, Zeid Yasiry","doi":"10.1136/bcr-2024-261079","DOIUrl":null,"url":null,"abstract":"<p><p>A late adolescent patient was admitted after a collapse and was found to have an intracranial haemorrhage due to an underlying midline arteriovenous malformation (AVM). The patient underwent trans-arterial squid embolisation of the AVM with good radiological resolution. 18 months later, the patient presented with new onset headaches. Cranial imaging demonstrated an enhancing lesion at the site of the previously thrombosed AVM in the corpus callosum. This was deemed to be a foreign body granuloma, a rare complication of intravascular embolisation of AVMs. The patient continued to have periodic imaging with subsequent scans demonstrating progressive changes in the granuloma and this was then resected surgically. We describe the natural history of the granuloma formation, outline the cranial imaging features associated with this rare condition and review the literature of similar cases.</p>","PeriodicalId":9080,"journal":{"name":"BMJ Case Reports","volume":"17 11","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Corpus callosum granuloma after endovascular squid embolisation of a ruptured arteriovenous malformation.\",\"authors\":\"Linford Fernandes, Fathallah Ismail Islim, Fozia Saeed, Tufail Patankar, Zeid Yasiry\",\"doi\":\"10.1136/bcr-2024-261079\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A late adolescent patient was admitted after a collapse and was found to have an intracranial haemorrhage due to an underlying midline arteriovenous malformation (AVM). The patient underwent trans-arterial squid embolisation of the AVM with good radiological resolution. 18 months later, the patient presented with new onset headaches. Cranial imaging demonstrated an enhancing lesion at the site of the previously thrombosed AVM in the corpus callosum. This was deemed to be a foreign body granuloma, a rare complication of intravascular embolisation of AVMs. The patient continued to have periodic imaging with subsequent scans demonstrating progressive changes in the granuloma and this was then resected surgically. We describe the natural history of the granuloma formation, outline the cranial imaging features associated with this rare condition and review the literature of similar cases.</p>\",\"PeriodicalId\":9080,\"journal\":{\"name\":\"BMJ Case Reports\",\"volume\":\"17 11\",\"pages\":\"\"},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2024-11-07\",\"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-2024-261079\",\"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-2024-261079","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Corpus callosum granuloma after endovascular squid embolisation of a ruptured arteriovenous malformation.
A late adolescent patient was admitted after a collapse and was found to have an intracranial haemorrhage due to an underlying midline arteriovenous malformation (AVM). The patient underwent trans-arterial squid embolisation of the AVM with good radiological resolution. 18 months later, the patient presented with new onset headaches. Cranial imaging demonstrated an enhancing lesion at the site of the previously thrombosed AVM in the corpus callosum. This was deemed to be a foreign body granuloma, a rare complication of intravascular embolisation of AVMs. The patient continued to have periodic imaging with subsequent scans demonstrating progressive changes in the granuloma and this was then resected surgically. We describe the natural history of the granuloma formation, outline the cranial imaging features associated with this rare condition and review the literature of similar cases.
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.