Extraosseous Ewing's Sarcoma of the Pancreas: An Uncommon but Treatable Disease

  • Saif M
  • Kaley K
N/ACitations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

Extraosseous Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) is a rare but aggressive and malignant tumor, and has been reported in various sites such as the lungs, biliary tract, kidney, prostate, stomach, esophagus, oral cavity, salivary glands, urinary bladder, uterus, cervix, gonads, and vagina. However, the pancreas is considered to be an extremely uncommon site and only a handful of cases have been published to date. We present here another case of a pancreatic ES/PNET. Our case intensifies the importance to recognize this rare type of tumor in the pancreas as there is a broad spectrum of tumors with a similar morphology that includes sheets of small, round blue cells. As observed in our present case, this problem is markedly challenged when the tumor site of origin is uncertain.

Cite

CITATION STYLE

APA

Saif, M. W., & Kaley, K. (2017). Extraosseous Ewing’s Sarcoma of the Pancreas: An Uncommon but Treatable Disease. Cureus. https://doi.org/10.7759/cureus.1882

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free