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A case of eosinophilic granulomatosis with polyangitis(EGPA)diagnosed through rupture of hepatic aneurysm Toru Otsuka 1 1Radiology Department Saga-Ken Medical Centre Koseikan Keyword: 好酸球性多発血管炎性肉芽腫症 , 肝動脈瘤 , 動脈瘤 pp.685-691
Published Date 2023/7/10
DOI https://doi.org/10.18888/rp.0000002390
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We report a 79-year-old female with asthma manifesting acute abdominal pain. Diagnosed with acute cholecystitis, she was treated with antibiotics. On day 9, she suffered from hypovolemic shock. Contrast-enhanced CT revealed hemorrhagic ascites with multiple intrahepatic and mesenchymal aneurysms;intrahepatic one was probably ruptured. Angiography showed countless intrahepatic and mesenchymal aneurysms, and transarterial embolization for the ruptured one was performed. She followed an uneventful course without developing any complications. On the basis of multiple intrahepatic and mesenchymal aneurysms, her history of asthma, and eosinophilia in blood test, she was diagnosed as EGPA.


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