From the Section of Neuroradiology, Department of Radiology, University of Alabama at Birmingham, Birmingham, Alabama.
From the Section of Neuroradiology, Department of Radiology, University of Alabama at Birmingham, Birmingham, Alabama
AJNR Am J Neuroradiol. 2021 Mar;42(3):404-413. doi: 10.3174/ajnr.A7015. Epub 2021 Jan 21.
Skull base osteomyelitis is a relatively rare condition, generally occurring as a complication of advanced otologic or sinus infection in immunocompromised patients. Skull base osteomyelitis is generally divided into 2 broad categories: typical and atypical. Typical skull base osteomyelitis occurs secondary to uncontrolled infection of the temporal bone region, most often from necrotizing external otitis caused by in a patient with diabetes. Atypical skull base osteomyelitis occurs in the absence of obvious temporal bone infection or external auditory canal infection. It may be secondary to advanced sinusitis or deep face infection or might occur in the absence of a known local source of infection. Atypical skull base osteomyelitis preferentially affects the central skull base and can be caused by bacterial or fungal infections. Clinically, typical skull base osteomyelitis presents with signs and symptoms of otitis externa or other temporal bone infection. Both typical and atypical forms can produce nonspecific symptoms including headache and fever, and progress to cranial neuropathies and meningitis. Early diagnosis can be difficult both clinically and radiologically, and the diagnosis is often delayed. Radiologic evaluation plays a critical role in the diagnosis of skull base osteomyelitis, with CT and MR imaging serving complementary roles. CT best demonstrates cortical and trabecular destruction of bone. MR imaging is best for determining the overall extent of disease and best demonstrates involvement of marrow space and extraosseous soft tissue. Nuclear medicine studies can also be contributory to diagnosis and follow-up. The goal of this article was to review the basic pathophysiology, clinical findings, and key radiologic features of skull base osteomyelitis.
颅底骨髓炎是一种相对罕见的疾病,通常发生于免疫功能低下的患者中耳或鼻窦感染的晚期并发症。颅底骨髓炎一般分为 2 大类:典型和非典型。典型颅底骨髓炎继发于颞骨区域失控的感染,最常见于糖尿病患者的坏死性外耳道炎引起的感染。非典型颅底骨髓炎在无明显颞骨感染或外耳道感染的情况下发生。它可能继发于严重的鼻窦炎或深部面部感染,也可能在无明确局部感染源的情况下发生。非典型颅底骨髓炎优先影响颅底中央,可由细菌或真菌感染引起。临床上,典型的颅底骨髓炎表现为外耳道炎或其他颞骨感染的体征和症状。典型和非典型形式都可产生非特异性症状,包括头痛和发热,并进展为颅神经病变和脑膜炎。临床和影像学诊断都很困难,诊断常常被延误。放射学评估在颅底骨髓炎的诊断中起着至关重要的作用,CT 和 MRI 成像发挥着互补的作用。CT 最能显示骨皮质和小梁的破坏。MRI 最适合确定疾病的整体范围,并最好显示骨髓空间和骨外软组织的受累情况。核医学研究也有助于诊断和随访。本文的目的是回顾颅底骨髓炎的基本病理生理学、临床发现和关键的放射学特征。