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Childhood hepatic angiosarcoma--a case report.

C S Premalata1, Rekha V Kumar, L Appaji

  • 1Department of Pathology, Kidwai Memorial Institute of Oncology, M.H. Marigowda Road, Bangalore. prema_venka@hotmail.com

Indian Journal of Pathology & Microbiology
|December 22, 2005
PubMed
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Hepatic angiosarcoma (HAS) is a rare childhood liver cancer. This case highlights its rarity and discusses the link between infantile hemangioendothelioma (IHE) and HAS.

Area of Science:

  • Pediatric oncology
  • Hepatobiliary pathology

Background:

  • Hepatic angiosarcoma (HAS) is exceptionally rare in pediatric populations.
  • Distinguishing HAS from other pediatric liver tumors can be challenging.

Observation:

  • A six-year-old girl presented with acute abdominal pain, fever, and an epigastric mass.
  • Initial clinical diagnosis was hepatoblastoma.
  • A left hepatic lobectomy was performed.

Findings:

  • Histopathological examination confirmed the diagnosis of hepatic angiosarcoma.
  • The findings underscore the importance of thorough histopathological analysis.

Implications:

  • This case emphasizes the rarity of childhood hepatic angiosarcoma.

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  • It prompts further discussion on the relationship between infantile hemangioendothelioma (IHE) and HAS.
  • Accurate diagnosis is crucial for appropriate management of pediatric liver tumors.