Small intestinal angiosarcoma on clinical presentation, diagnosis, management and prognosis:
A case report and review of the literature - PMC Back to Top Skip to main content NIH NLM …

Angiosarcoma is a rare disease with a poor prognosis; significantly, patients with intestinal
angiosarcomas who survive over 1 year after diagnosis are extraordinarily rare. This article …

Angiosarcoma is an aggressive mesenchymal sarcoma of endothelial cell origin with high
mortality. Its occurrence in the small intestine is exceedingly low. In addition to the rarity of …

Abstract Primary Gastrointestinal Angiosarcoma (PGAS) constitutes a rare malignant tumor
arising from vascular or lymphatic endothelial cells. The aim of this study was to review the …

Angiosarcoma is a rare form of soft tissue sarcoma. Primary small intestinal angiosarcomas
are especially uncommon. The clinical presentations of small intestinal angiosarcomas vary …

Introduction Intestinal angiosarcomas are an extremely rare and aggressive vascular
tumors, with a few cases reported in the literature. Presentation of case A 45 years-old male …

Primary malignant tumors of the small intestine are rare, comprising less than 2% of all
gastrointestinal tumors. An 85-year-old woman was admitted with fever of 40 C and marked …

Angiosarcomas are aggressive neoplasms that arise from endothelial cells and can develop
in any part of the body. Gastrointestinal angiosarcomas are very uncommon and can have a …

Angiosarcomas developing in unusual sites such as the small bowel are rare, and fewer
than 65 cases have been reported in the literature. They are not uncommonly associated …

A man in his 40s presented to an emergency department after experiencing worsening
abdominal pain for 2 days. Contrast-enhanced CT of the abdomen and pelvis revealed …