Neurosyphilis (NS) is an infection of the central nervous system, caused by the invasion of Treponema pallidum, which can occur in any stage of syphilis, particularly in the late stages of the disease. 1 NS presents with various clinical features, such as mimicking early onset Alzheimer's disease (AD), mild frontotemporal dementia (FTD) or primary psychiatric disease (PPD). 1-3 Brain magnetic resonance imaging (B-MRI) features seen in NS vary, and are usually presented as cerebral infarction, sulci widening, global/hippocampal predominant atrophy, white matter lesions, or meningitis. 4-7 Recently, diffuse temporoparietal hypometabolism and spared thalamic metabolism, in fluorodeoxy-glucose-positron emission tomography (FDG-PET), have been reported as new findings in NS. 3 In the current case report, the authors describe a patient with NS, who exhibited varied and complex clinical symptoms. B-MRI showed severe atrophy, involving bilateral medial temporal lobes (MTL), and abnormalities were detected in FDG-PET scan.
CASE REPORTA 49-year-old male patient was hospitalized with a history of psychiatric manifestations since 10 months, personality changes, and progressive cognitive impairments. The patient had a history of exhibiting depressive behavior and at times anger, for about 10 months before admission. He also displayed the habit of repeating words and frequently mentioning past episodes. Sometimes, during conversations, the patient interrupted inappropriately or spoke on irrelevant subjects.Approximately 7-month before hospitalization, the patient experienced delusion and insomnia. He believed he was a genius with an IQ of 190. Occasionally,The clinical features and brain magnetic resonance image (B-MRI) findings in neurosyphilis (NS) are highly varied. Cortical atrophy, especially involving the medial temporal lobes (MTL), is a remarkable radiographic feature, reported in B-MRI scans, in cases of NS presenting with severe cognitive impairments. The observed MTL atrophy is similar to the atrophy seen in neurodegenerative disorders such as Alzheimer's disease (AD) or frontotemporal dementia (FTD). A fluorodeoxy-glucose-positron emission tomography (FDG-PET), used for the diagnosis of AD, commonly reveals global cortical hypometabolism, sparing basal ganglia and thalamus, in NS. We report a case of NS, with complex symptoms and bilateral MTL atrophy. FDG-PET imaging showed bilateral thalamic and right visual cortical glucose reduction, as well as diffuse cortical hypometabolism. This type of FDG-PET pattern is a new finding in the field of NS. FIG. 2. Fluorodeoxy-glucose-positron emission tomography. (A) Hypometabolism observed in bilateral frontal, parietal, and temporal lobes (more prominent on the right) (black arrows), and thalamus (white arrows). (B) Statistical parametric mapping analysis showing the hypometabolism in bilateral frontal, parietal, and temporal lobes, compared with age-matched controls. A B 176 http://www.j-nn.org