Pulmonary tumor thrombotic microangiopathy from metastatic epithelioid angiosarcoma

Funda Demirag1, Ebru Cakir, Ulku Yazici

  • 1Atatürk Chest Diseases and Chest Surgery Education and Research Hospital, Department of Pathology, Ankara, Turkey;

Insights

Metastatic epithelioid angiosarcoma can cause pulmonary tumor thrombotic microangiopathy. Tumor cells expressing VEGF and topoisomerase II suggest potential therapeutic targets for this rare lung condition.

Area of Science:

  • Oncology
  • Pulmonary Medicine
  • Pathology

Background:

  • The lung is a frequent site for cancer metastasis through the bloodstream.
  • Tumor emboli lodging in lung vessels can lead to intimal proliferation, a hallmark of pulmonary tumor thrombotic microangiopathy (PTTM).
  • PTTM is rarely diagnosed before death.

Observation:

  • A case of a 60-year-old woman with metastatic epithelioid angiosarcoma involving the lung is presented.
  • Histopathological examination revealed tumor emboli within lung vasculature.
  • Tumor cells were found to be positive for Vascular Endothelial Growth Factor (VEGF) and topoisomerase II.

Findings:

  • The observed fibrocellular and fibromuscular intimal proliferation is consistent with PTTM.
  • VEGF expression in tumor cells may play a role in the development of PTTM.
  • Topoisomerase II positivity indicates potential sensitivity to specific therapeutic inhibitors.

Implications:

  • This case highlights the importance of considering PTTM in patients with metastatic cancer to the lung.
  • VEGF and topoisomerase II may represent therapeutic targets for managing PTTM.
  • Early diagnosis and targeted therapies could improve outcomes for patients with this rare condition.

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