Malignant primary cardiac tumors in childhood and adolescence

被引:4
作者
Fresneau, B. [1 ]
Oberlin, O. [1 ]
Brugieres, L. [1 ]
Valteau-Couanet, D. [1 ]
Patte, C. [1 ]
机构
[1] Inst Gustave Roussy, Serv Oncol Pediat, F-94800 Villejuif, France
来源
ARCHIVES DE PEDIATRIE | 2010年 / 17卷 / 05期
关键词
B-CELL LYMPHOMAS; PEDIATRIC-ONCOLOGY; EXPERIENCE; DIAGNOSIS; CHILDREN; INVOLVEMENT; SURVIVAL; SOCIETY; TRIAL; HEART;
D O I
10.1016/j.arcped.2010.02.009
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Primary heart tumors are uncommon in children. The majority of them are benign, with only 10% malignant. Among malignant cardiac tumors, sarcoma (rhabdomyosarcoma, align sarcoma, synovial sarcoma) and lymphoma (Burkitt's lymphoma, large B-cell lymphoma, lymphoblastic lymphoma) predominate. There are few published pediatric series on malignant primary cardiac tumors. We report here 3 observations of primary malignant cardiac tumors, 2 cases of sarcoma (angiosarcoma and synovial sarcoma) and 1 case of Burkitt's lymphoma. A precise pathological diagnosis is necessary for the proper management of these patients. For sarcoma, treatment associates surgery and chemotherapy. Surgery should be as complete as possible because of the lack of chemotherapy sensitivity of some sarcomas, mainly angiosarcoma and synovial sarcoma. The the prognosis of cardiac sarcoma remains poor. For primary cardiac lymphoma, management should not he different from lymphoma in other locations. Chemotherapy is the main treatment, and surgery has to be used only when complications occur. Prognosis depends on histology and not lymphoma location, and so is better than the prognosis for sarcoma. (C) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:495 / 501
页数:7
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