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Primary care challenges of an obscure case of “Alice in Wonderland” syndrome in a patient with severe malaria in a resource-constrained setting: a case report

机译:在资源有限的情况下,患有严重疟疾的患者中“爱丽丝梦游仙境(Alice in Wonderland)”综合征的一例晦涩病例的初级保健挑战:一例病例报告

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“Alice in Wonderland” syndrome (AIWS) is a rare neurological abnormality characterized by distortions of visual perceptions, body schema and experience of time. AIWS has been reported in patients with various infections such as infectious mononucleosis, H1N1 influenza, Cytomegalovirus encephalitis, and typhoid encephalopathy. However, AIWS occurring in a patient with severe malaria is less familiar and could pose serious primary care challenges in a low-income context. A 9-year-old male of black African ethnicity was brought by his parents to our primary care hospital because for 2?days he had been experiencing intermittent sudden perceptions of his parents’ heads and objects around him either “shrinking” or “expanding”. The visual perceptions were usually brief and resolved spontaneously. One week prior to the onset of the visual problem, he had developed an intermittent high grade fever that was associated with other severe constitutional symptoms. Based on the historical and clinical data that were acquired, severe malaria was suspected and this was confirmed by hyperparasitaemia on blood film analysis. The patient was treated with quinine for 10?days. Apart from a single episode of generalized tonic-clonic seizures that was observed on the first day of treatment, the overall?clinical progress was good. The visual illusions completely resolved and no further abnormalities were recorded during 3?months of follow-up. Symptoms of AIWS usually resolve spontaneously or after treatment of an underlying cause. In our case, the successful treatment of severe malaria coincided with a complete regression of AIWS whose aetiology was poorly-elucidated given the resource constraints. In any case, the good outcome of our patient aligns with previous reports on acute AIWS that highlight a limited need for excessive investigation and treatment modalities which are, in passing, predominantly unaffordable in resource-limited primary care settings.
机译:“爱丽丝梦游仙境”综合症(AIWS)是一种罕见的神经系统异常,其特征是视觉感知,身体模式和时间经历的扭曲。据报道,AIWS可用于多种感染的患者,例如传染性单核细胞增多症,H1N1流感,巨细胞病毒性脑炎和伤寒性脑病。然而,在严重疟疾患者中发生的AIWS较不为人所知,并且在低收入情况下可能构成严重的初级保健挑战。一名9岁的非洲黑人种族男性,其父母将其带到我们的初级保健医院,因为他连续2天对自己父母的头部和周围物体感到断断续续的突然“收缩”或“扩张” 。视觉感受通常是短暂的并且自发地解决。视觉问题发作前一周,他出现了间歇性高烧,并伴有其他严重的体质症状。根据获得的历史和临床数据,怀疑有严重的疟疾,这在血膜分析中被高寄生虫血症所证实。病人接受奎宁治疗10天。在治疗的第一天,除了观察到单发的强直阵挛性癫痫发作外,总体临床进展良好。视力错觉完全消失,在随访的3个月内未发现任何异常。 AIWS的症状通常会自发缓解或在治疗根本原因后解决。在我们的案例中,重症疟疾的成功治疗与AIWS的完全消退相吻合,而AIWS的病因学在资源有限的情况下难以阐明。无论如何,我们患者的良好结果与先前关于急性AIWS的报道相吻合,该报道强调了对过度调查和治疗方式的有限需求,而这些手段通常在资源有限的初级保健环境中是负担不起的。

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