Osteosarcoma with Cardiac Metastasis in a 22-year-old Man: A Case Report and Review of Cardiac Tumors

被引：6

作者：

Pinder, Marco ^{[1
]}

CharafEddine, Ahmad ^{[2
]}

Parnell, Aimee S. ^{[2
]}

DiBardino, Daniel J. ^{[3
]}

Knudson, Jarrod D. ^{[4
,5
]}

机构：

[1] Univ Mississippi, Med Ctr, Batson Childrens Hosp, Dept Pediat, Jackson, MS 39216 USA

[2] Univ Mississippi, Med Ctr, Batson Childrens Hosp, Dept Pediat,Div Cardiol, Jackson, MS 39216 USA

[3] Univ Mississippi, Med Ctr, Batson Childrens Hosp, Dept Surg,Div Congenital Heart Surg, Jackson, MS 39216 USA

[4] Univ Mississippi, Med Ctr, Blair E Batson Hosp Children, Dept Pediat,Div Crit Care, Jackson, MS 39216 USA

[5] Univ Mississippi, Med Ctr, Blair E Batson Hosp Children, Div Cardiol, Jackson, MS 39216 USA

来源：

CONGENITAL HEART DISEASE | 2014年 / 9卷 / 05期

关键词：

Cardiac Tumors; Osteosarcoma; Cardiac Surgery; MULTICENTER EXPERIENCE; TUBEROUS SCLEROSIS; OSTEOGENIC-SARCOMA; CHILDREN; HEART; MALIGNANCIES; RHABDOMYOMA; DIAGNOSIS; NEONATE; FETAL;

D O I：

10.1111/chd.12113

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Primary osteosarcoma accounts for 3% of all childhood cancer. It commonly occurs during the adolescent growth spurt and is more common in boys than girls and in African Americans than white people. The 5-year survival is approximately 79%. Cardiac metastasis of osteosarcoma is exceedingly rare; we present an unusual case in a 22-year-old man with significant intracardiac tumor burden. Additionally, we review the current pediatric cardiac tumor literature.

引用

页码：E147 / E152

页数：6

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