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Updated: Jul 5, 2026

Laparoscopic Anatomical Right Hemihepatectomy via the In Situ Anterior Approach
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Published on: August 8, 2025

Hepatic angiosarcoma manifested as recurrent hemoperitoneum.

Seung-Woo Lee1, Chun-Young Song, Young-Hwa Gi

  • 1Division of Gastroenterology and Hepatology, Department of Internal Medicine, Dae Jeon St. Mary's Hospital, The Catholic University of Korea, 520-2 Dae Heung Dong, Joong Gu, Dae Jeon, Seoul 301-723, Korea.

World Journal of Gastroenterology
|May 14, 2008
PubMed
Summary

We present a rare case of primary hepatic angiosarcoma, a fast-progressing liver cancer. This uncommon tumor presented unusually as recurrent hemoperitoneum, highlighting diagnostic challenges.

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Area of Science:

  • Hepatobiliary Medicine
  • Surgical Oncology
  • Gastroenterology

Background:

  • Angiosarcoma is a rare malignancy, comprising less than 1% of all sarcomas.
  • Primary hepatic angiosarcoma is exceptionally rare and often presents with vague symptoms.
  • This aggressive cancer is associated with a high mortality rate.

Observation:

  • The case involved recurrent hemoperitoneum, an uncommon presentation for liver tumors.
  • Initial symptoms were nonspecific, delaying diagnosis.
  • The patient presented with a rare manifestation of primary hepatic angiosarcoma.

Findings:

  • The diagnosis of primary hepatic angiosarcoma was confirmed.
  • The tumor's presentation as recurrent hemoperitoneum is a key finding.
  • Rapid progression and high mortality are characteristic of this condition.

Implications:

  • This case underscores the importance of considering rare diagnoses in patients with unexplained hemoperitoneum.
  • Early recognition of hepatic angiosarcoma is crucial for potential intervention, despite its rarity.
  • Further research into the diagnostic and therapeutic strategies for rare liver cancers is warranted.