TY - JOUR
T1 - Undifferentiated embryonal sarcoma of the liver successfully treated with chemotherapy and liver resection
AU - Baron, Pedro W.
AU - Majlessipour, Fatenah
AU - Bedros, Antranik A.
AU - Zuppan, Craig W.
AU - Ben-Youssef, Ramzi
AU - Yanni, George
AU - Ojogho, Okechukwu N.
AU - Concepcion, Waldo
N1 - Funding Information:
Acknowledgement This work was supported by a grant from the Loma Linda Transplantation Institute, Loma Linda, CA.
PY - 2007/1
Y1 - 2007/1
N2 - Undifferentiated embryonal sarcoma is the third most common malignant tumor of the liver in children, accounting for 13% of hepatic malignancies in this age group. It has been considered an aggressive neoplasm with very poor prognosis until the late 1980s, when long-term survivors were reported after multiagent chemotherapy followed by resection. We, herein, report two pediatric cases of undifferentiated embryonal sarcoma treated successfully with surgical resection after neoadjuvant chemotherapy based on therapy used in childhood soft tissue sarcomas and in childhood hepatic malignancies. The first patient also had a concurrent cerebellar tumor (pilocytic astrocytoma), for which he first underwent craniotomy and resection, delaying the liver tumor resection by 10 weeks. They are alive and tumor free at 48 months (case no. 1) and 18 months (case no. 2) following neoadjuvant chemotherapy and liver resection. © The Society for Surgery of the Alimentary Tract 2007.
AB - Undifferentiated embryonal sarcoma is the third most common malignant tumor of the liver in children, accounting for 13% of hepatic malignancies in this age group. It has been considered an aggressive neoplasm with very poor prognosis until the late 1980s, when long-term survivors were reported after multiagent chemotherapy followed by resection. We, herein, report two pediatric cases of undifferentiated embryonal sarcoma treated successfully with surgical resection after neoadjuvant chemotherapy based on therapy used in childhood soft tissue sarcomas and in childhood hepatic malignancies. The first patient also had a concurrent cerebellar tumor (pilocytic astrocytoma), for which he first underwent craniotomy and resection, delaying the liver tumor resection by 10 weeks. They are alive and tumor free at 48 months (case no. 1) and 18 months (case no. 2) following neoadjuvant chemotherapy and liver resection. © The Society for Surgery of the Alimentary Tract 2007.
KW - Cerebellar tumor
KW - Chemotherapy
KW - Liver resection
KW - Malignant liver tumor
KW - Humans
KW - Sarcoma/drug therapy
KW - Male
KW - Combined Modality Therapy
KW - Hepatectomy
KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use
KW - Adolescent
KW - Liver Neoplasms/drug therapy
KW - Neoadjuvant Therapy
KW - Child
UR - https://www.scopus.com/pages/publications/34250201488
UR - https://www.scopus.com/pages/publications/34250201488#tab=citedBy
UR - https://www.mendeley.com/catalogue/48dd6c13-3dbe-322c-8300-7fd41f616c44/
U2 - 10.1007/s11605-006-0044-4
DO - 10.1007/s11605-006-0044-4
M3 - Article
C2 - 17390190
SN - 1091-255X
VL - 11
SP - 73
EP - 75
JO - Journal of Gastrointestinal Surgery
JF - Journal of Gastrointestinal Surgery
IS - 1
ER -