Kim Ealmaan
Division of Skull Base Surgery, Department of Neurosurgery, Keimyung University School of Medicine, Dongsan Medical Center, Daegu, Korea.
J Korean Neurosurg Soc. 2010 Nov;48(5):441-4. doi: 10.3340/jkns.2010.48.5.441. Epub 2010 Nov 30.
Fibrous dysplasia (FD) of craniofacial structures is well documented, however, its involvement of the clivus is seldom described. We report a case of clival FD in a young man who presented with headache localized to the occipital area. The radiological studies revealed a monostotic disease confined to the clivus, with typical findings of hypointensity on magnetic resonance images and ground-glass density on computed tomography. The diagnosis of FD was confirmed on pathological examination of specimens taken through transsphenoidal surgery. The patient showed reduction of symptoms and no change of residual lesion on follow-up imaging taken 2.5 years later after surgery. This study includes clinical aspect, radiographic appearance, differential diagnosis and treatment strategy of this rare skull base lesion.
颅面结构的骨纤维异常增殖症(FD)已有充分记载,然而,其累及斜坡的情况却鲜有描述。我们报告一例年轻男性斜坡FD病例,该患者表现为局限于枕部区域的头痛。影像学研究显示为局限于斜坡的单骨型病变,在磁共振成像上有典型的低信号表现,在计算机断层扫描上有磨玻璃样密度。通过经蝶窦手术获取的标本经病理检查确诊为FD。患者术后2.5年的随访影像显示症状减轻,残余病变无变化。本研究涵盖了这种罕见颅底病变的临床情况、影像学表现、鉴别诊断及治疗策略。