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一名曾接受尤因肉瘤治疗的患者的骨肉瘤诊断。

Diagnosis of osteosarcoma in a patient previously treated for Ewing sarcoma.

作者信息

Hoshi Manabu, Ieguchi Makoto, Yamato Kazumi, Tokimasa Sadao, Nakamura Hiroaki

机构信息

Department of Orthopedic Surgery, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-Machi, Abeno-Ku, Osaka, 545-8585, Japan,

出版信息

Skeletal Radiol. 2014 Sep;43(9):1319-24. doi: 10.1007/s00256-014-1880-z. Epub 2014 Apr 11.

Abstract

Primary malignant bone tumors, whether Ewing sarcoma or osteosarcoma, are a rare type of tumor. The sequential occurrence of two bone sarcomas, Ewing sarcoma and high-grade osteosarcoma, in the same patient at two different locations is an exceptionally rare phenomenon. We present the case of a 13-year-old girl who presented with a high-grade osteoblastic osteosarcoma of the distal femur, 7 years after treatment for Ewing sarcoma of the left pelvis. She did not receive radiation therapy. Following the recent developing multidisciplinary therapy, long-term follow-up for monitoring latent treatment-related adverse effects may be necessary for survivors of primary malignant bone tumors.

摘要

原发性恶性骨肿瘤,无论是尤因肉瘤还是骨肉瘤,都是一种罕见的肿瘤类型。在同一患者的两个不同部位先后发生两种骨肉瘤,即尤因肉瘤和高级别骨肉瘤,是一种极其罕见的现象。我们报告了一例13岁女孩的病例,她在接受左骨盆尤因肉瘤治疗7年后,出现了股骨远端的高级别成骨细胞性骨肉瘤。她未接受放射治疗。随着近期多学科治疗的发展,对于原发性恶性骨肿瘤幸存者而言,长期随访以监测潜在的治疗相关不良反应可能是必要的。

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