Whatley T G, Brown P C, Frew A L
J Oral Surg. 1979 Feb;37(2):117-9.
The case presented here represents an aggressive form of polyostotic fibrous dysplasia. Because of lack of evidence to substantiate precocious puberty and abnormal pigmentation, Albright syndrome cannot be established. Because of the nature of this disease, its clinical course and prognosis are unpredictable. However, it is believed that continued growth of the lesion may necessitate additional surgery.
此处呈现的病例代表了一种侵袭性的多骨型纤维性发育不良。由于缺乏证据证实性早熟和色素沉着异常，故无法确诊为奥尔布赖特综合征。鉴于这种疾病的性质，其临床病程和预后难以预测。然而，据信病变的持续生长可能需要进一步手术。
