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双侧视网膜母细胞瘤后发生的骨干毛细血管扩张性骨肉瘤作为第二原发肿瘤。

Diaphyseal telangiectatic osteosarcoma as a second tumor after bilateral retinoblastomas.

作者信息

Brown M J, Logan P M, O'Connell J X, Janzen D L, Connell D G

机构信息

Department of Radiology, University of British Columbia, Vancouver, Canada.

出版信息

Skeletal Radiol. 1996 Oct;25(7):685-8. doi: 10.1007/s002560050160.

Abstract

In this report, we describe the clinical, imaging, and pathologic findings in a case of diaphyseal telangiectatic osteosarcoma arising 23 years after successful treatment of bilateral retinoblastomas. To our knowledge, telangiectatic osteosarcoma occurring as a second tumor in this setting, outside the radiation treatment field, has not been previously reported. The association of the RB-1 gene defect with retinoblastomas and other tumors is discussed. Also, the computed tomography and magnetic resonance imaging findings in telangiectatic osteosarcoma are described and discussed.

摘要

在本报告中,我们描述了一例双侧视网膜母细胞瘤成功治疗23年后发生的骨干毛细血管扩张性骨肉瘤的临床、影像学和病理表现。据我们所知,在这种情况下,作为第二肿瘤发生在放疗野之外的毛细血管扩张性骨肉瘤此前尚未见报道。本文还讨论了RB-1基因缺陷与视网膜母细胞瘤及其他肿瘤的关联。此外,还描述并讨论了毛细血管扩张性骨肉瘤的计算机断层扫描和磁共振成像表现。

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