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Hepatic angiosarcoma in a child: successful therapy with surgery and adjuvant chemotherapy.

Abstract
We report a 3-year and 11-month-old Caucasian female, who initially presented with an unresectable hepatic angiosarcoma. After three courses of chemotherapy with adriamycin/cisplatin, the tumor decreased in size considerably, allowing complete surgical resection. She also received postoperative chemotherapy with alternating cycles of ifosfamide/etoposide, cisplatinum/adriamycin, and vincristine/actinomycin D/cyclophosphamide for 18 months. She remains disease-free for greater than 44 months from the initial diagnosis. Our experience suggests that total excision of the tumor, together with an aggressive chemotherapy regimen, can improve the disease-free survival for children with this highly malignant vascular tumor of the liver.
AuthorsS W Gunawardena, L M Trautwein, M J Finegold, A K Ogden
JournalMedical and pediatric oncology (Med Pediatr Oncol) Vol. 28 Issue 2 Pg. 139-43 (Feb 1997) ISSN: 0098-1532 [Print] United States
PMID8986151 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Dactinomycin
  • Vincristine
  • Etoposide
  • Doxorubicin
  • Cyclophosphamide
  • Cisplatin
  • Ifosfamide
Topics
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Chemotherapy, Adjuvant
  • Child, Preschool
  • Cisplatin (administration & dosage)
  • Combined Modality Therapy
  • Cyclophosphamide (administration & dosage)
  • Dactinomycin (administration & dosage)
  • Doxorubicin (administration & dosage)
  • Drug Administration Schedule
  • Etoposide (administration & dosage)
  • Female
  • Hemangiosarcoma (drug therapy, surgery)
  • Humans
  • Ifosfamide (administration & dosage)
  • Liver Neoplasms (drug therapy, surgery)
  • Vincristine (administration & dosage)

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