Cystic Presentation of Primary Hepatic Angiosarcoma
نویسندگان
چکیده
Chand, Jithin T.; Kumar, Arun; Sebastian, George M.; Appukuttan, Murali Author Information
منابع مشابه
Hepatic angiosarcoma. Presentation of two cases.
Hepatic angiosarcoma is a rare primary tumor of the liver with a mesenchymal origin. Diagnosis is difficult because clinical manifestations and imaging studies are inconclusive. In many cases a diagnosis is obtained during necropsy, not being apparent during the course of disease. It is associated with several risk factors, but these contribute to explaining only a few of all reported cases. Wh...
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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...
متن کاملFulminant 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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1Department of Dermatology, Venereology & Leprology, SMGS Hospital, Government Medical College, University of Jammu, Jammu-180001 Jammu & Kashmir, India, 2Department of Pathology, SMGS Hospital, Government Medical College, University of Jammu, Jammu-180001 Jammu & Kashmir, India, 3Department of Radio-Diagnosis, SMGS Hospital, Government Medical College, University of Jammu, Jammu-180001 Jammu &...
متن کاملPrimary hepatic angiosarcoma: difficulty in clinical, radiological, and pathological diagnosis.
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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ژورنال
عنوان ژورنال: Formosan Journal of Surgery
سال: 2023
ISSN: ['1682-606X', '2213-5413']
DOI: https://doi.org/10.1097/fs9.0000000000000066