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神经囊尾蚴病

Neurocysticercosis.

作者信息

Mukherjee A, Roy T, Mukherjee S, Basu N, Duttamunshi A

机构信息

Bangur Institute of Neurology.

出版信息

J Assoc Physicians India. 1993 May;41(5):287-9.

PMID:8300463
Abstract

Sixty-two cases of neurocysticercosis (NCC) were examined over a period of five years. Convulsive seizure was the commonest presentation (57%). The other modes of presentation included features of raised intracranial pressure (19%) meningoencephalitis (9%), "Stroke" like onset (4%) and progressive dementia (6%). Clinical signs were scanty. Six patients had papilloedema, five had hemiparesis while three had isolated cranial nerve palsies. Soft tissue calcification and mucocutaneous nodules were infrequent and was found in 13 (21%) and 5 cases (8%) respectively. Clinical suspicion supported by CT scan and Immunobiologic tests using ELISA were the mainstay in diagnosis. Praziquantel and Albendazole were found effective in the treatment of neurocysticercosis, but because of serious side effects encountered in some cases, the drugs should be used cautiously in selected cases only.

摘要

在五年时间里对62例神经囊尾蚴病(NCC)患者进行了检查。惊厥发作是最常见的表现形式(57%)。其他表现形式包括颅内压升高(19%)、脑膜脑炎(9%)、“卒中”样起病(4%)和进行性痴呆(6%)。临床体征较少。6例患者有视乳头水肿,5例有偏瘫,3例有孤立的脑神经麻痹。软组织钙化和皮肤黏膜结节不常见,分别在13例(21%)和5例(8%)中发现。临床怀疑并经CT扫描及使用酶联免疫吸附测定(ELISA)的免疫生物学检测支持是诊断的主要依据。吡喹酮和阿苯达唑被发现对神经囊尾蚴病有效,但由于在某些病例中出现严重副作用,这些药物仅应在特定病例中谨慎使用。

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