一例神经梅毒并发全身瘫痪且同时感染艾滋病毒但未获治疗的特殊病例

O. T. D. Perera, K. Ranasinghe, B. Gk, M. Wimalarathna, G. D. K. N. Karunarathna, S. C. Wijesiriwardena, Senior Consultant Psychiatrist C K Ranasinghe, T. D. Perera
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引用次数: 0

摘要

精神错乱性全身瘫痪或麻痹性痴呆是神经梅毒一种罕见的常规表现。在青霉素和艾滋病毒时代,观察和诊断神经梅毒的典型表现是一项挑战。42岁的单身男性出现了急性行为障碍,在快速发展的健忘和功能退化的背景下听到了声音,以至于日常生活需要他人帮助,小便失禁持续了9个月。他的精神变化最初始于令人痛苦的失眠,导致每天饮酒 30 单位。调查显示,在扩展认知评估中,额叶和优势顶叶功能明显受损。血液检查显示,患者患有正常红细胞性贫血,炎症指标升高:CRP、ESR、CPK升高,甲状腺功能正常。梅毒血清学检查呈阳性。随后,眼科医生进行的检查发现了眼部梅毒。脑脊液分析梅毒呈阴性,这些变化很可能与未经治疗的艾滋病毒感染有关,CD4细胞计数为104个/μL。神经影像学检查显示他全身皮质萎缩,脑室扩大。他在接受神经梅毒治疗的同时,也开始接受艾滋病毒治疗,但病情改善甚微:结论:神经梅毒仍然是年轻患者快速进展性痴呆的重要病因。结论:神经梅毒仍然是年轻患者快速进展性痴呆症的重要病因,合并艾滋病病毒感染会加重病情的严重性和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A peculiar case of neurosyphilis presenting with general paresis of the insane with concurrent untreated HIV infection
General paresis of insane or dementia paralytica is a rare conventional manifestation of neurosyphilis. In the era of penicillin and HIV it is a challenge to observe and diagnose typical presentations of neurosyphilis.42-year-old single male presented with an acute behavioural disturbance with hearing voices in a background of rapidly progressing forgetfulness and functional deterioration to the extent of needing support for his activities of daily living with urine incontinence for nine months duration. His beha-vioural change had first started with distressing insomnia leading to consumption of alcohol 30 units a day. Gradually displayed disorganised and dis-inhibited behaviour with some overactivity and was treated as a mood disorder with poor response and rapid deterioration of functioning.Investigations revealed marked impairment of frontal lobe and dominant parietal lobe functions in extended cognitive assessment. Blood investigations revealed normocytic normochromic anaemia with raised inflammatory markers: CRP, ESR, CPK with normal thyroid function. Syphilis serology was positive. Subsequently the examination carried out by an eye surgeon detected ocular syphilis. CSF analysis was negative for syphilis and the changes were most likely related to the untreated HIV infection with a CD4 count of 104 cells/μL. Neuroimaging showed generalized cortical atrophy with enlarged ventricles. He was treated for neurosyphilis as well as and treatment for HIV was initiated, but there was minimal improvement.Conclusions: Neurosyphilis remains as an important aetiology to be considered in rapidly progressing dementia in young patients. Comorbid HIV infection worsens the severity and prognosis.
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