Surgically Diagnosed Primary Hepatic Angiosarcoma

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Surgically Diagnosed Primary Hepatic Angiosarcoma

Primary hepatic angiosarcoma is a rare tumor originating from endothelial cells in the liver and accounts for approximately 1% of all hepatic malignant tumors. It is difficult to diagnose due to the lack of specific symptoms or tumor markers. No effective treatment exists, but complete surgical resection may achieve a good outcome. Since most primary hepatic angiosarcomas are already at an adva...

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Fulminant Hepatic Failure Secondary to Primary Hepatic Angiosarcoma

Background. Hepatic angiosarcoma is a rare and aggressive tumor that often presents at an advanced stage with nonspecific symptoms. Objective. To report a case of primary hepatic angiosarcoma in an otherwise healthy man with normal liver function tests two months prior to presenting with a short period of jaundice that progressed to fulminant hepatic failure. Methods. Case report and review of ...

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Hepatic angiosarcoma is a rare primary mesenchymal malignancy. Prognosis is poor and mortality occurs early. The diagnosis is challenging. Our case was an asymptomatic 70 year-old man referred, with incidental ultrasonography finding of multiple liver nodules. Diagnostic laparoscopic liver biopsy and the histopathological examination reported a haemangioma. Six months later, he became symptomat...

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A 64-year-old man presented with a 2monthhistoryofmelena.Healsohadahistory of chronic renal disease, hypertension, and diabetes mellitus, and he had worked at a leather factory for decades. He was diagnosed as having primary hepatic angiosarcoma and had undergone right lobectomy 4 months before this admission. Esophagogastroduodenoscopy and colonoscopy failed todetect thebleeding source. Capsul...

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ژورنال

عنوان ژورنال: Internal Medicine

سال: 2018

ISSN: 0918-2918,1349-7235

DOI: 10.2169/internalmedicine.9318-17