Case of Primary Hepatic Angiosarcoma Presenting With Jaundice and Infiltrative Liver Masses

Adnan Shaaban, Chimaobi Anugwom, Alma Habib, Tetyana Mettler, Shahid Jaffer, Mary Thomson

Research output: Contribution to journalArticlepeer-review

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 languageEnglish (US)
JournalJournal of Investigative Medicine High Impact Case Reports
Volume10
DOIs
StatePublished - 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

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