{"title":"一例罕见的获得性A型血友病合并大疱性类天疱疮并发脑真菌脓肿和多重机会性感染","authors":"Maffi G","doi":"10.52768/2379-1039/1989","DOIUrl":null,"url":null,"abstract":"Acquired A Haemophilia (AHA) is a rare autoimmune disease caused by production of anti VIII factors antibodies that could cause multiple haemorrhagic manifestations. Usually idiopathic, could be related with other conditions, such as Bullous Pemphigoid (BP), an autoimmune dermatologic disease.","PeriodicalId":90942,"journal":{"name":"Open journal of clinical & medical case reports","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A rare case of acquired A haemophilia associated with bullous pemphigoid complicated by cerebral fungal abscesses and multiple opportunistic infections\",\"authors\":\"Maffi G\",\"doi\":\"10.52768/2379-1039/1989\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Acquired A Haemophilia (AHA) is a rare autoimmune disease caused by production of anti VIII factors antibodies that could cause multiple haemorrhagic manifestations. Usually idiopathic, could be related with other conditions, such as Bullous Pemphigoid (BP), an autoimmune dermatologic disease.\",\"PeriodicalId\":90942,\"journal\":{\"name\":\"Open journal of clinical & medical case reports\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Open journal of clinical & medical case reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.52768/2379-1039/1989\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open journal of clinical & medical case reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52768/2379-1039/1989","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A rare case of acquired A haemophilia associated with bullous pemphigoid complicated by cerebral fungal abscesses and multiple opportunistic infections
Acquired A Haemophilia (AHA) is a rare autoimmune disease caused by production of anti VIII factors antibodies that could cause multiple haemorrhagic manifestations. Usually idiopathic, could be related with other conditions, such as Bullous Pemphigoid (BP), an autoimmune dermatologic disease.