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Unusual Neurological Complication Of Typhoid Fever

机译:伤寒的异常神经系统并发症

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A 36-year-old male with typhoid fever presented with conduction aphasia and parietal lobe dysfunction due to an infarct in the left posterior parieto-temporal cortex documented by CT Scan. This case highlights an unusual neurological complication of typhoid fever hitherto not reported in the literature. Introduction Typhoid fever caused by Salmonella group of organisms has a high prevalence in tropical countries of Asia and Africa. Classically described clinical manifestations are rarely encountered due to early diagnosis and institution of antibiotic therapy. Of all the complications described in typhoid fever, the neuropsychiatric manifestations are the most varied and fascinating for the medical world. Here we present a case of typhoid fever developing cortical infarction with aphasia and parietal lobe dysfunction. Case Report A 36-year-old male was admitted to the hospital with 20 days history of fever and headache. He was receiving treatment before admission to our hospital as typhoid fever based on positive Widal test (initial titre 1:80 later 1:320) with ciprofloxacin and gentamycin. On the day of admission, there was history of sudden onset of giddiness with altered sensorium for one hour. Following this, the patient became responsive but was unable to communicate freely due to reduced word output for which he was brought to the hospital.Clinical examination showed an anxious, febrile (39.6° C) patient with mild splenomegaly. The patient was conscious, well oriented, with well-preserved comprehension for spoken words, but had severely impaired naming and repetition. No focal motor deficit was present. All primary modalities of sensations were intact. However, tactile localization and two-point discrimination were impaired on right half of the body. Parietal lobe dysfunction was documented by presence of dyscalculia, ideational apraxia with inattention to tactile and auditory stimulation. Right to left disorientation and finger anomia were also present. Reading and writing could not be tested in detail, as the patient was not literate, and could write only his name. No visual field defect was documented.Haemoglobin concentration was 15.3g/dL, white blood cell count was 6900cells/mm3, platelet count was 2,18,000/mm3 and ESR was 20mm in the first hour. Biochemical parameters were normal. Chest X-ray was normal. Mantoux test and serology for HIV were negative. Malaria and urinary tract infections were ruled out.A diagnosis of typhoid fever was considered in view of Widal test being strongly positive (1:640 titer after admission for both somatic and flagellar antigen). A rising titer was also documented. Blood cultures were sterile, probably due to prior antibiotic therapy.CT scan of the brain revealed a hypo-dense lesion involving the left posterior parieto-temporal cortex suggestive of an early infarct (Figure 1). Lumbar puncture showed normal opening pressure and CSF analysis revealed no abnormality.
机译:一名患有伤寒的36岁男性因CT扫描记录到左后顶颞颞皮层梗塞而出现传导性失语和顶叶功能障碍。该病例突出了迄今为止文献中尚未报道的伤寒异常神经系统并发症。简介由沙门氏菌群引起的伤寒在亚洲和非洲的热带国家盛行。由于早期诊断和采用抗生素治疗,很少会遇到经典描述的临床表现。在伤寒描述的所有并发症中,神经精神病学表现是医学界最多样化,最令人着迷的。在这里,我们介绍了一例伤寒导致发展为失语和顶叶功能障碍的皮层梗死。病例报告一名36岁的男性入院,有20天的发烧和头痛病史。在入院前,他接受环丙沙星和庆大霉素的阳性Widal试验(初次滴度为​​1:80,之后为1:320)接受伤寒治疗。在入院当天,有突然发作的头晕史,感觉改变了一个小时。此后,患者反应灵敏,但由于单词输出减少而无法自由交流,因此他被送往医院。临床检查显示,一名焦虑,发热(39.6°C)的患者患有轻度脾肿大。病人意识清晰,方向明确,对口头语言的理解力得到很好的保护,但严重损害了命名和重复能力。没有聚焦运动障碍。感觉的所有主要方式均完好无损。但是,在身体的右半部有触觉定位和两点歧视。顶叶功能障碍的存在是由于粘膜粘连症,概念性失用症以及不重视触觉和听觉刺激而引起的。从右到左迷失方向和手指异常也存在。阅读和写作无法详细测试,因为患者不识字,只能写自己的名字。没有发现视野缺损。第一小时血红蛋白浓度为15.3g / dL,白细胞计数为6900cells / mm3,血小板计数为2,18,000 / mm3,ESR为20mm。生化指标正常。胸部X线检查正常。 Mantoux测试和HIV血清学检查均为阴性。排除了疟疾和尿路感染。考虑到Widal试验呈强阳性(体细胞和鞭毛抗原均以1:640滴度滴定),因此诊断为伤寒。滴度也有记录。血液培养物是无菌的,可能是由于先前的抗生素治疗所致。脑部CT扫描显示低密度病变,累及左后顶颞颞皮层,提示早期梗死(图1)。腰椎穿刺显示打开压力正常,CSF分析未发现异常。

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