TY - JOUR
T1 - Extraosseous Ewing's sarcoma of the pancreas
AU - Bose, Prithviraj
AU - Murugan, Paari
AU - Gillies, Elizabeth
AU - Holter, Jennifer L.
PY - 2012/8
Y1 - 2012/8
N2 - The Ewing's family of tumors (EFT) comprises a molecularly defined group of ''small round blue cell tumors'', consisting of Ewing's sarcoma of bone (ESB), extraosseous Ewing's sarcoma (EES), peripheral primitive neuroectodermal tumor (pPNET), and Askin's tumor. Characteristic translocations that disrupt the EWSR1 gene located at 22q12 create novel fusion genes that are central to the pathogenesis. The EFT also shares certain clinical characteristics, such as a peak incidence during the teenage years, a tendency to spread rapidly, and responsiveness to the same chemotherapeutic regimens and radiation therapy. Nearly all patients have occult disseminated disease at diagnosis; hence, chemotherapy is routinely used. Improvements in multimodality treatment have had a dramatic impact on outcomes. EES/pPNET has been reported in a variety of sites, including the pancreas, though this is extremely rare. We describe a case of pancreatic EES/ pPNET in a 35-year-old woman and provide a brief review of the relevant literature.
AB - The Ewing's family of tumors (EFT) comprises a molecularly defined group of ''small round blue cell tumors'', consisting of Ewing's sarcoma of bone (ESB), extraosseous Ewing's sarcoma (EES), peripheral primitive neuroectodermal tumor (pPNET), and Askin's tumor. Characteristic translocations that disrupt the EWSR1 gene located at 22q12 create novel fusion genes that are central to the pathogenesis. The EFT also shares certain clinical characteristics, such as a peak incidence during the teenage years, a tendency to spread rapidly, and responsiveness to the same chemotherapeutic regimens and radiation therapy. Nearly all patients have occult disseminated disease at diagnosis; hence, chemotherapy is routinely used. Improvements in multimodality treatment have had a dramatic impact on outcomes. EES/pPNET has been reported in a variety of sites, including the pancreas, though this is extremely rare. We describe a case of pancreatic EES/ pPNET in a 35-year-old woman and provide a brief review of the relevant literature.
KW - Ewing's sarcoma
KW - Extraosseous Ewing's sarcoma
KW - PNET
KW - Pancreas
KW - Primitive neuroectodermal tumor
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U2 - 10.1007/s10147-011-0311-6
DO - 10.1007/s10147-011-0311-6
M3 - Article
C2 - 21892669
AN - SCOPUS:84867336293
SN - 1341-9625
VL - 17
SP - 399
EP - 406
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 4
ER -