Daly B D, Chow C C, Cockram C S
Department of Diagnostic Radiology and Organ Imaging, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, N.T.
Postgrad Med J. 1994 Jan;70(819):10-6. doi: 10.1136/pgmj.70.819.10.
Clinical, endocrinological and computed tomographic features of three patients with unusual manifestations or complications of craniofacial involvement of fibrous dysplasia are presented. One patient with polyostotic fibrous dysplasia presented in late pregnancy with acute onset of bilateral optic nerve compression and blindness secondary to a rapidly expanding mass of fibrous dysplasia tissue involving the sphenoid, pituitary and optic chiasm regions. A second patient with polyostotic fibrous dysplasia developed thyrotoxicosis and probable gigantism/acromegaly in keeping with a rare form of McCune-Albright syndrome. Extensive bony distortion of the skull and facial bones by fibrous dysplasia made clinical recognition of these complications more difficult. A third patient had monostotic fibrous dysplasia with marked sclerosis of the sphenoid bone on plain radiographs which mimicked appearances of a meningioma and resulted in a negative craniotomy as computed tomography was not yet available at the time of presentation. Each case demonstrated rare complications of craniofacial fibrous dysplasia and highlighted the wide spectrum of appearances in which it may manifest, often resulting in overlap and diagnostic confusion with other disease processes. The value of computed tomography in assessment is emphasized.
本文介绍了3例纤维结构不良累及颅面部出现异常表现或并发症患者的临床、内分泌及计算机断层扫描特征。1例多骨型纤维结构不良患者在妊娠晚期出现急性双侧视神经受压及失明,继发于蝶骨、垂体和视交叉区域纤维结构不良组织迅速增大的肿块。第2例多骨型纤维结构不良患者发生甲状腺毒症及可能的巨人症/肢端肥大症,符合一种罕见的麦库恩-奥尔布赖特综合征。纤维结构不良导致颅骨和面部骨骼广泛骨质变形,使这些并发症的临床识别更加困难。第3例患者为单骨型纤维结构不良,平片显示蝶骨明显硬化,类似脑膜瘤表现,由于就诊时尚无计算机断层扫描,导致开颅手术结果为阴性。每个病例均显示了颅面部纤维结构不良的罕见并发症,并突出了其可能出现的广泛表现,常导致与其他疾病过程重叠及诊断混淆。强调了计算机断层扫描在评估中的价值。