Primary hepatic angiosarcoma mistaken for a giant hemangioma
Primary hepatic angiosarcoma (PHA) is a rare hepatic mesenchymal tumor that accounts for 2% of all primary malignant liver tumors. It typically presents with nonspecific symptoms, is highly aggressive, and there are limited treatment options. Imaging characteristics of PHA overlap with that of hepatic hemangioma, a common benign hepatic lesion, creating a potential diagnostic pitfall. We present a case of PHA that mimicked hepatic hemangioma on imaging. We review the differentiating characteristics between these two hepatic tumors. PHAs demonstrate irregular/infiltrating margins, higher lesion multiplicity, higher risk of tumor rupture, and rapid growth, which are not typically seen with hepatic hemangiomas.
Authors
- Mitchell P. Wilson (ORCID: https://orcid.org/0000-0002-1630-5138)
- Gavin Low (ORCID: https://orcid.org/0000-0002-4959-8934)
- Safwat Girgis
- Xu Jing Qian (ORCID: https://orcid.org/0009-0009-7805-0562)
Institutions
- University of Alberta Hospital (CA)
Publication Details
- Journal
- Intractable & Rare Diseases Research
- Published
- 2024-12-20
- DOI
- https://doi.org/10.5582/irdr.2024.01045
- Primary Topic
- Vascular Tumors and Angiosarcomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00