Kadia Benjamin Momo, Ekabe Cyril Jabea, Agborndip Ettamba
Foumbot District Hospital, Foumbot, Cameroon.
Grace Community Health and Development Association, Kumba, Cameroon.
BMC Infect Dis. 2017 Dec 22;17(1):789. doi: 10.1186/s12879-017-2918-3.
"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.
“爱丽丝梦游仙境综合征”(AIWS)是一种罕见的神经异常,其特征为视觉感知、身体形象和时间体验的扭曲。AIWS已在患有各种感染的患者中被报道,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,AIWS出现在重症疟疾患者中则鲜为人知,并且在低收入环境中可能给初级保健带来严重挑战。
一名9岁的非洲裔黑人男性被父母带到我们的初级保健医院,因为两天来他一直间歇性地突然感觉他父母的头部以及周围的物体要么“缩小”要么“变大”。这些视觉感知通常很短暂且会自行缓解。在视觉问题出现前一周,他出现了间歇性高热,并伴有其他严重的全身症状。根据所获取的病史和临床资料,怀疑为重症疟疾,血涂片分析发现高寄生虫血症证实了这一诊断。该患者接受了10天的奎宁治疗。除了在治疗第一天观察到一次全身性强直阵挛发作外,总体临床进展良好。视觉幻觉完全消失,在3个月的随访期间未记录到进一步的异常情况。
AIWS的症状通常会自行缓解或在治疗潜在病因后缓解。在我们的病例中,重症疟疾的成功治疗与AIWS的完全消退同时发生,鉴于资源限制,其病因难以明确。无论如何,我们患者的良好预后与先前关于急性AIWS的报道一致,这些报道强调在资源有限的初级保健环境中,过度检查和治疗方式的需求有限,而这些方式通常难以负担。