Zreik Riyam T, Littrell Laurel A, Jin Long, Oliveira Andre M, Fritchie Karen J
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905.
Department of Radiology, Mayo Clinic, Rochester, MN 55905.
Hum Pathol. 2017 Apr;62:170-174. doi: 10.1016/j.humpath.2016.09.030. Epub 2016 Oct 19.
Malignant transformation of fibrous dysplasia (FD) is exceedingly rare, occurring in less than 1% of all FD cases, and has been described in both monostotic and polyostotic forms of this entity. We report a case of a large proximal femur mass arising in a 45-year-old man. The biopsy revealed a high-grade pleomorphic malignancy that focally expressed multiple keratins. Based on the presence of keratin immunoreactivity, the morphologic differential diagnosis included metastatic sarcomatoid carcinoma. However, review of the clinical information revealed a history of polyostotic FD, and imaging findings were compatible with malignant transformation of FD. The resected neoplasm was biphasic and composed of areas of conventional FD admixed with a high-grade pleomorphic malignancy. Activating GNAS mutations were identified in both components. To the best of our knowledge, this is the first description of keratin expression in malignant transformation of FD.
骨纤维异常增殖症(FD)的恶变极为罕见,在所有FD病例中发生率不到1%,且在单骨型和多骨型FD中均有报道。我们报告一例发生于一名45岁男性的近端股骨巨大肿块病例。活检显示为高级别多形性恶性肿瘤,局部表达多种角蛋白。基于角蛋白免疫反应性的存在,形态学鉴别诊断包括转移性肉瘤样癌。然而,回顾临床资料发现有多骨型FD病史,影像学表现与FD恶变相符。切除的肿瘤为双相性,由传统FD区域与高级别多形性恶性肿瘤混合组成。在两个成分中均检测到激活的GNAS突变。据我们所知,这是首次描述FD恶变中角蛋白的表达情况。