Literature DB >> 8986151

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

S W Gunawardena1, L M Trautwein, M J Finegold, A K Ogden.   

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.

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Year:  1997        PMID: 8986151     DOI: 10.1002/(sici)1096-911x(199702)28:2<139::aid-mpo9>3.0.co;2-l

Source DB:  PubMed          Journal:  Med Pediatr Oncol        ISSN: 0098-1532


  2 in total

Review 1.  The role of liver transplantation in the management of paediatric liver tumours.

Authors:  Mark D Stringer
Journal:  Ann R Coll Surg Engl       Date:  2007-01       Impact factor: 1.891

2.  Clinical characteristics of primary hepatic angiosarcoma outcomes: a SEER database analysis.

Authors:  Dong Zeng; Xianghua Zeng; Jun Duan; Diangang Chen; Bo Zhu
Journal:  Transl Cancer Res       Date:  2021-01       Impact factor: 1.241

  2 in total

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