Calleja Michele, Amary Fernanda, O'Donnell Paul
Department of Radiology, The Royal National Orthopaedic Hospital, Stanmore, HA7 4LP, UK.
Department of Histopathology, The Royal National Orthopaedic Hospital, Stanmore, UK.
Skeletal Radiol. 2019 Jan;48(1):151-157. doi: 10.1007/s00256-018-2975-8. Epub 2018 May 27.
Mazabraud's syndrome is a rare disorder characterised by the association of fibrous dysplasia with intramuscular myxomas. We present a 36-year-old woman with right anterior knee pain and a buttock mass. Imaging showed aggressive bone destruction within an area of fibrous dysplasia in the right femur and a mass with myxoid signal characteristics in the right adductor region. Biopsy of the femur revealed both fibrous dysplasia and a high-grade spindle cell sarcoma. Biopsy of the adductor mass confirmed a soft-tissue myxoma. Molecular genetic analysis revealed an identical R201H substitution in the GNAS1 gene in the sarcoma, the myxoma, and also the conventional fibrous dysplasia.
马扎布罗综合征是一种罕见的疾病,其特征为骨纤维发育不良与肌内黏液瘤并存。我们报告一名36岁女性,有右膝前部疼痛和臀部肿块。影像学检查显示右股骨骨纤维发育不良区域内有侵袭性骨质破坏,右内收肌区域有一个具有黏液样信号特征的肿块。股骨活检显示既有骨纤维发育不良又有高级别梭形细胞肉瘤。内收肌肿块活检证实为软组织黏液瘤。分子遗传学分析显示,肉瘤、黏液瘤以及传统的骨纤维发育不良中GNAS1基因均存在相同的R201H替代突变。