Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan 812-8582.
Hum Pathol. 2013 Jun;44(6):1184-9. doi: 10.1016/j.humpath.2012.11.011. Epub 2013 Jan 31.
Bone infarct-associated sarcoma is a rare sarcoma, accounting for less than 1% of all bone sarcomas. Its histology usually reflects a high-grade sarcoma, such as malignant fibrous histiocytoma of bone or conventional osteosarcoma. Low-grade sarcoma arising from bone infarct has not been described well in the literature. Here, we present a 17-year follow-up of a female patient with bone infarct in her right humerus, from which a low-grade central osteosarcoma developed during follow-up. A histologic diagnosis of low-grade central osteosarcoma was confirmed by immunohistochemical expression of MDM2 and CDK4. She underwent a wide resection surgery. As of 4 years after surgery, she has remained free of any evidence of recurrence or metastasis. Here, we present clinical and pathologic findings of our case in detail and discuss the differential diagnoses of this extremely rare condition.
骨梗死相关肉瘤是一种罕见的肉瘤,占所有骨肉瘤的比例不到 1%。其组织学通常反映出高级别的肉瘤,如骨恶性纤维组织细胞瘤或常规骨肉瘤。文献中尚未很好地描述源于骨梗死的低级别的肉瘤。在此,我们报告了一名女性患者的 17 年随访结果,该患者右侧肱骨有骨梗死,随访过程中发展为低度中央型骨肉瘤。通过免疫组织化学表达 MDM2 和 CDK4 证实了低度中央型骨肉瘤的组织学诊断。她接受了广泛的切除术。手术后 4 年,她没有任何复发或转移的迹象。在此,我们详细介绍了我们病例的临床和病理发现,并讨论了这种极其罕见情况的鉴别诊断。