Primary pulmonary epithelioid angiosarcoma: A case report and literature review

J Cancer Res Ther. 2018 Jun;14(Supplement):S533-S535. doi: 10.4103/0973-1482.176419.

Abstract

Primary pulmonary epithelioid angiosarcoma is an extremely rare malignancy. Herein, we report the case of an elderly Chinese patient with primary pulmonary epithelioid angiosarcoma. The 72-year-old man presented with a 1-month history of persistent hemoptysis and left chest pain and weight loss of 3 kg. A chest computed tomography (CT) scan revealed two masses (maximum size 3.0 cm × 2.0 cm and 0.8 cm × 0.5 cm) in right lower lobe. We performed a left thoracotomy for tumor resection. Pathological examination showed that there was a significant amount of hemorrhage, fibrinous exudates, degeneration, and necrosis. With immunohistochemical analysis, tumor cells had strong expression of CD34, FLI-1, vimentin. Morphological and immunohistochemical findings supported the diagnosis of epithelioid angiosarcoma.

Keywords: Angiosarcoma; epithelioid; immunohistochemistry; pathology; pulmonary.

Publication types

  • Case Reports
  • Letter
  • Review

MeSH terms

  • Aged
  • Biopsy
  • Combined Modality Therapy
  • Hemangiosarcoma / diagnosis*
  • Hemangiosarcoma / metabolism
  • Hemangiosarcoma / therapy
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms / diagnosis*
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / therapy
  • Male
  • Tomography, X-Ray Computed
  • Treatment Outcome