Crone M D, Wallace R G
Musgrave Park Hospital, Belfast, UK.
Skeletal Radiol. 1990;19(4):245-50. doi: 10.1007/BF00191665.
The radiographic features of a unique autosomal dominant bone dysplasia are presented. The features are classified as generalised and/or focal. Generalised features are either altered trabecular pattern or modelling abnormalities. Focal features comprise lytic areas which progressively enlarge, producing expansion of the bone and eventual disintegration due to fibrous and finally fatty replacement of the normal medulla. Almost 90% of these lesions occur in the appendicular skeleton. Clinically, hearing loss is the earliest manifestation of the disease, presenting sometimes as early as 4 years of age. Apical and cervical resorption of teeth is extremely common, resulting in premature loss of teeth. Radiologically, the differential diagnosis refers to Paget's disease, polyostotic fibrous dysplasia, and osteofibrous dysplasia. The progressive destruction of the bone is similar to massive osteolysis (Gorham's disease). The radiographic features in combination with the histopathology render the condition unique.
本文介绍了一种独特的常染色体显性骨发育不良的影像学特征。这些特征分为全身性和/或局灶性。全身性特征包括小梁模式改变或塑形异常。局灶性特征包括溶骨性区域,其逐渐扩大,导致骨质膨胀,最终由于正常骨髓被纤维组织取代并最终被脂肪组织取代而崩解。这些病变几乎90%发生在四肢骨骼。临床上,听力丧失是该病最早的表现,有时早在4岁时就会出现。牙齿根尖和颈部吸收极为常见,导致牙齿过早脱落。在放射学上,鉴别诊断包括佩吉特病、多骨纤维发育不良和骨纤维发育不良。骨质的进行性破坏类似于大块骨质溶解(戈勒姆病)。影像学特征与组织病理学相结合使得该病症独具特色。