Wu R K, Trumble T E, Ruwe P A
Department of Orthopaedics and Rehabilitation, Yale University School of Medicine, New Haven, Connecticut.
Clin Orthop Relat Res. 1991 Apr(265):306-9.
This report describes a family of three siblings with a long history of polyostotic Paget's disease. Because of the severe osseous involvement with Paget's disease, all three patients had problems that required orthopedic surgery. Subsequent to these surgeries, two patients developed osteogenic sarcoma at sites unrelated to their past procedures, one in the sacrum and one in the calvarium. Both patients died shortly after their diagnosis because of the aggressive spread of the tumor. Although the etiology of Paget's disease and its complication of osteogenic sarcoma still remain to be clarified, this and other case reports suggest a possible environmental or hereditary contribution to developing osteogenic sarcoma in Paget's disease. Patients with a familial clustering of polyostotic Paget's disease may benefit from more thorough screening tests to detect malignant transformation.
本报告描述了一个有三兄弟姐妹的家庭,他们患有多骨型佩吉特病的病史很长。由于佩吉特病严重累及骨骼,所有三名患者都有需要进行骨科手术的问题。这些手术后,两名患者在与过去手术无关的部位发生了骨肉瘤,一名在骶骨,一名在颅骨。两名患者在诊断后不久因肿瘤的侵袭性扩散而死亡。尽管佩吉特病及其骨肉瘤并发症的病因仍有待阐明,但本病例报告和其他病例报告表明,在佩吉特病中发生骨肉瘤可能存在环境或遗传因素。有多骨型佩吉特病家族聚集性的患者可能受益于更全面的筛查测试以检测恶性转化。