Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Mar 1;43(2):e203-e206.
doi: 10.1097/MPH.0000000000001674.

Pediatric Metastatic Cardiac Angiosarcoma Successfully Treated With Multimodal Therapy: Case Report and Review of Literature

Affiliations
Review

Pediatric Metastatic Cardiac Angiosarcoma Successfully Treated With Multimodal Therapy: Case Report and Review of Literature

Jane Koo et al. J Pediatr Hematol Oncol. .

Abstract

Cardiac angiosarcoma (AS) is an extremely rare, malignant vascular tumor with <10 cases reported in the pediatric literature. Prognosis is dismal with overall survival often <1 year from initial diagnosis. In this report, we present the case of a 10-year-old boy with metastatic cardiac AS who is currently alive and is the longest pediatric survivor of metastatic cardiac AS reported in the literature. This is the only published pediatric case to successfully use a combination of surgical resection, conventional chemotherapy, radiation and targeted therapies including bevacizumab and pazopanib for metastatic cardiac AS.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Fresneau B, Oberlin O, Brugieres L, et al. Malignant primary cardiac tumors in childhood and adolescence. Arch Pediatr. 2010;17:495–501.
    1. Bien E, Stachowicz-Stencel T, Balcerska A, et al. Angiosarcoma in children—still uncontrollable oncological problem. The report of the Polish Paediatric Rare Tumours Study. Eur J Cancer Care (Engl). 2009;18:411–420.
    1. Ayadi L, Khabir A. Pediatric angiosarcoma of soft tissue: a rare clinicopathologic entity. Arch Pathol Lab Med. 2010;134:481–485.
    1. Abraham JA, Hornicek FJ, Kaufman AM, et al. Treatment and outcome of 82 patients with angiosarcoma. Ann Surg Oncol. 2007;14:1953–1967.
    1. Yu K, Liu Y, Wang H, et al. Epidemiological and pathological characteristics of cardiac tumors: a clinical study of 242 cases. Interact Cardiovasc Thorac Surg. 2007;6:636–639.

MeSH terms