Chang Patrick C, Fischbein Nancy J, Holliday Roy A
Department of Radiology, University of California, San Francisco, School of Medicine, San Francisco, CA 94143, USA.
AJNR Am J Neuroradiol. 2003 Aug;24(7):1310-6.
Skull base osteomyelitis typically arises as a complication of ear infection in older diabetic patients, involves the temporal bone, and has Pseudomonas aeruginosa as the usual pathogen. Atypical skull base osteomyelitis arising from the sphenoid or occipital bones without associated external otitis occurs much less frequently and initially may have headache as the only symptom. The purpose of this study was to review the clinical and MR imaging features of central skull base osteomyelitis.
We retrospectively reviewed MR images obtained in six patients with central skull base osteomyelitis. No patient had predisposing external otitis or osteomyelitis of the temporal bone.
All of our patients presented with headache, no external ear pain, and cranial nerve deficits. Five of six patients had a predisposition to infection, and the erythrocyte sedimentation rate was elevated in the five patients in whom it was checked. In each case, the diagnosis was delayed until MR imaging demonstrated central skull base abnormality, and the diagnosis was then confirmed with tissue sampling. The most consistent imaging findings were clival bone marrow T1 hypointensity and preclival soft tissue infiltration. Five of six patients were cured with no recurrence of skull base infection over a 2-4-year follow-up period.
In the setting of headache, cranial neuropathy, elevated erythrocyte sedimentation rate, and abnormal clival imaging findings, central skull base osteomyelitis should be considered as the likely diagnosis. Early tissue sampling and appropriate treatment may prevent or limit further complications such as intracranial extension, empyema, or death.
颅底骨髓炎通常发生于老年糖尿病患者,是耳部感染的并发症,累及颞骨,常见病原体为铜绿假单胞菌。由蝶骨或枕骨引发且无外耳道炎的非典型颅底骨髓炎较为少见,初期可能仅以头痛为唯一症状。本研究旨在回顾中央颅底骨髓炎的临床及磁共振成像(MR)特征。
我们回顾性分析了6例中央颅底骨髓炎患者的MR图像。所有患者均无外耳道炎或颞骨骨髓炎的易感因素。
所有患者均有头痛症状,无耳部疼痛及颅神经功能缺损。6例患者中有5例存在感染易感性,5例患者的红细胞沉降率检查结果升高。每例患者在MR成像显示中央颅底异常之前诊断均被延误,之后经组织取样确诊。最一致的影像学表现为斜坡骨髓T1加权像低信号及斜坡前软组织浸润。6例患者中有5例在2至4年的随访期内治愈,颅底感染无复发。
在出现头痛、颅神经病变、红细胞沉降率升高及斜坡影像学异常的情况下,应考虑中央颅底骨髓炎为可能的诊断。早期组织取样及适当治疗可预防或限制进一步的并发症,如颅内蔓延、积脓或死亡。