Chandrasekharan Rajsekar, Kulkarni Chinmay, Pullara Sreekumar Karumathil, Moorthy Srikanth
Department of Radiology, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala.
Indian J Radiol Imaging. 2022 Jun 30;32(2):278-284. doi: 10.1055/s-0042-1744523. eCollection 2022 Jun.
We report magnetic resonance imaging (MRI) in a case with otosyphilis, which is a rare manifestation of neurosyphilis. A 50-year-old male presented with progressive hearing loss on the left side and recent-onset palsy of the left 7th and 12th cranial nerves. Computed tomography imaging showed destructive bone lesions involving the petrous temporal bone, middle ear, and mastoid region with a pathognomonic pattern of bone destruction depicted in the volume rendering technique images. MRI showed features of destructive bone lesions (gummatous lesion), meningoneuritis, and labyrinthitis. Pathological examination and treponemal antibody absorption test favored the diagnosis. Otosyphilis should be considered as a differential diagnosis in an adult patient with destructive lesions of the petrous temporal bone. To the best of our knowledge, MRI in otosyphilis has not been reported.
我们报告了一例耳梅毒的磁共振成像(MRI)表现,耳梅毒是神经梅毒的一种罕见表现。一名50岁男性,出现左侧进行性听力丧失以及近期新发的左侧第7和第12颅神经麻痹。计算机断层扫描成像显示岩颞骨、中耳和乳突区域有破坏性骨病变,容积再现技术图像呈现出特征性的骨破坏模式。MRI显示有破坏性骨病变(树胶样肿病变)、脑膜神经炎和迷路炎的特征。病理检查和梅毒螺旋体抗体吸收试验支持该诊断。对于患有岩颞骨破坏性病变的成年患者,应考虑耳梅毒作为鉴别诊断。据我们所知,尚未有耳梅毒的MRI报道。