International Journal of Colorectal Disease

, Volume 23, Issue 8, pp 745–756

Rapidly progressive metastatic multicentric epithelioid angiosarcoma of the small bowel: a case report and a review of literature

Authors

    • Department of Internal MedicineSt. Joseph Mercy Hospital
  • Amudha R. M. Daniel
    • Department of Internal MedicineSt. Joseph Mercy Hospital
  • Erik J. Carson
    • Division of Hematology and Oncology, Department of Internal MedicineSt. Joseph Mercy Hospital
  • Andrew T. Catanzaro
    • Division of Gastroenterology, Department of Internal MedicineSt. Joseph Mercy Hospital
  • Thomas M. Shehab
    • Division of Gastroenterology, Department of Internal MedicineSt. Joseph Mercy Hospital
  • Joseph A. Tworek
    • Department of PathologySt. Joseph Mercy Hospital
Review

DOI: 10.1007/s00384-007-0420-x

Cite this article as:
Grewal, J.S., Daniel, A.R.M., Carson, E.J. et al. Int J Colorectal Dis (2008) 23: 745. doi:10.1007/s00384-007-0420-x

Abstract

Background

Angiosarcoma is a rare high-grade neoplasm that frequently involves the skin and subcutaneous tissue. Rarely, angiosarcoma can occur in the gastrointestinal tract where it frequently exhibits multicentric epithelioid morphology.

Design

We report a case of multicentric epithelioid angiosarcoma (EAS) of the small intestine in a 73-year-old male patient who presented with weakness and melena, and was found to have bleeding lesions in the small intestine on upper gastrointestinal endoscopy. In addition to this case, we extensively reviewed the clinical and pathological features of previously reported cases of angiosarcoma of the small intestine in the English literature since 1970.

Results

Our patient presented with rare and aggressive EAS of the small intestine. Despite surgical resection of the lesions, the patient continued to worsen and developed rapidly progressive metastatic disease. He died within 4 months of the diagnosis.

Conclusions

Angiosarcoma, especially of the deep tissues and the gastrointestinal tract, is very aggressive and rapidly metastatic. The survival rate in these patients is extremely poor, and most patients die within 6 months to 1 year of the diagnosis. Treatment usually involves surgical resection of the bleeding lesions and frequent blood transfusions for symptom alleviation.

Keywords

Epithelioid angiosarcomaSmall intestine

Copyright information

© Springer-Verlag 2007