Key result
A 39-year-old male liver transplant recipient developed de novo hepatic angiosarcoma 7.5 years post-transplant, presenting with atypical imaging findings including retention of gadoxetate disodium on MRI.
Why the study?
De novo primary hepatic angiosarcoma is exceedingly rare in transplanted livers, with only one previous case reported, and diagnosis is challenging due to non-specific presentation and overlapping imaging findings.
Case Report (n=1)
Highlights the diagnostic complexities and imaging findings of an exceedingly rare de novo hepatic angiosarcoma in a transplanted liver.
Warrants consideration of angiosarcoma in atypical post-transplant liver lesions; leaves open standardized diagnostic criteria and surveillance.
De novo primary hepatic angiosarcoma is an exceedingly rare malignancy in transplanted livers. Only 1 previous case has been reported in the literature. The diagnosis is usually challenging due to non-specific clinical presentation and overlapping imaging findings with other conditions. These rapidly progressing, multifocal lesions have previously been described to have varied growth patterns but are typically hypo-enhancing on gadoxetate disodium (Primovist) enhanced MRI. Surgical resection and adjuvant chemotherapy are potential options of treatment for hepatic angiosarcomas. Despite this, prognosis of patients at diagnosis is extremely poor. In this report we present imaging findings of a liver transplant recipient despite biopsy-confirmed hepatic angiosarcoma, and discuss the diagnostic complexities involved.
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Chow et al. (2025) conducted a case report in Hepatic angiosarcoma (n=1). Liver transplantation and immunosuppression was evaluated. A 39-year-old male liver transplant recipient developed de novo hepatic angiosarcoma 7.5 years post-transplant, presenting with atypical imaging findings including retention of gadoxetate disodium on MRI.
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