Reis C, Genden E M, Bederson J B, Som P M
Department of Neuroradiology, S. João University Hospital, Porto, Portugal.
Br J Radiol. 2008 Feb;81(962):e31-4. doi: 10.1259/bjr/19620568.
A 52-year-old man with long-standing craniofacial polyostotic fibrous dysplasia (FD) and no history of prior radiation therapy developed a spontaneous right temporal bone osteosarcoma. Such spontaneous sarcomatous degeneration of FD is rare, particularly in the calvarium/skull, where, to our knowledge, only six prior cases have been reported in the literature. We report this case because it is a rare entity with well-documented CT and MR images, and to emphasize the importance of depicting imaging features of sarcomatous degeneration among the complex imaging findings of FD.
一名52岁男性,患有长期的颅面多骨型纤维发育不良(FD),且无既往放疗史,发生了自发性右颞骨骨肉瘤。FD的这种自发性肉瘤样变性很罕见,尤其是在颅骨,据我们所知,文献中仅报道过6例先前病例。我们报告此病例是因为它是一种罕见的疾病,有详细记录的CT和MR图像,并且强调在FD复杂的影像学表现中描绘肉瘤样变性影像学特征的重要性。