表现为米-古二氏综合征的神经囊尾蚴病。

Neurocysticercosis presenting as Millard Gubler syndrome.

作者信息

Prasad Rajniti, Kapoor Kanika, Srivastava Arvind, Mishra Op

机构信息

Department of Pediatrics, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India.

出版信息

J Neurosci Rural Pract. 2012 Sep;3(3):375-7. doi: 10.4103/0976-3147.102634.

DOI:10.4103/0976-3147.102634

PMID:23189006

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3505345/

Abstract

Neurocysticercosis is a common childhood neurological illness in India. A variety of presentations have been reported in the literature, including weber syndrome. Neurocysticercosis, manifesting as Millard Gubler syndrome, have not been reported in literature. Therefore, we report a child presented to us with Millard Gubler syndrome due to pontomedullary neurocysticercosis and was treated successfully.

摘要

神经囊尾蚴病是印度常见的儿童神经疾病。文献报道了多种表现形式，包括韦伯综合征。而以米拉德·古布勒综合征表现的神经囊尾蚴病，文献中尚未见报道。因此，我们报告一名因桥延髓神经囊尾蚴病出现米拉德·古布勒综合征的儿童，并成功治愈。