Abstract
Primary hepatic angiosarcoma (PHA) is a rare and aggressive mesenchymal liver tumor with a poor prognosis and high mortality. Treatment options are limited to palliative chemotherapy with surgical resection reserved for the few cases that present early. We present a case of a patient who presented with jaundice and elevated liver enzymes. Imaging identified a diffusely heterogeneous liver consistent with cirrhosis, findings of portal hypertension, and 2 ill-defined liver lesions. Biopsy results confirmed PHA. Primary hepatic angiosarcoma does not have a typical presentation but should be considered for any patient presenting with an infiltrative liver mass.
Original language | English (US) |
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Journal | Journal of Investigative Medicine High Impact Case Reports |
Volume | 10 |
DOIs | |
State | Published - 2022 |
Bibliographical note
Publisher Copyright:© 2022 American Federation for Medical Research.
Keywords
- abnormal liver enzymes
- hepatic angiosarcoma
- malignant liver tumor
- mortality
PubMed: MeSH publication types
- Case Reports
- Journal Article