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颅后窝囊尾蚴病

Cysticercosis in the posterior cranial fossa.

作者信息

Cheepsattayakorn R, Tantachamroon T

机构信息

Department of Pathology, Faculty of Medicine, Chiang Mai University, Thailand.

出版信息

J Med Assoc Thai. 1994 Oct;77(10):544-8.

PMID:7745377
Abstract

Two cases of neurocysticercosis from Maharaj Nakorn Chiang Mai Hospital were reported with autopsy and surgical findings. The autopsy case was a 14-year-old girl who had a single cyst at the cisterna ambiens of the pineal region, causing hydrocephalus and severe brain edema accompanied with increased intracranial pressure and psychiatric problems but no definite localizing signs. The surgical case was a 35-year-old man with symptoms of increased intracranial pressure, localizing signs of ataxia of the left lower extremity and hearing loss in the right ear. Computed brain tomography showed a posterior fossa cyst with obstructive hydrocephalus. The cyst and the tissues from CP angle region were removed and sent to the Department of Pathology. Histopathologic appearance of both cases showed cysticercosis.

摘要

报告了清迈玛哈拉吉医院的两例神经囊尾蚴病病例,并给出了尸检和手术结果。尸检病例是一名14岁女孩,松果体区环池有单个囊肿,导致脑积水和严重脑水肿,伴有颅内压升高和精神问题,但无明确的定位体征。手术病例是一名35岁男性,有颅内压升高症状、左下肢共济失调定位体征和右耳听力丧失。脑部计算机断层扫描显示后颅窝囊肿伴梗阻性脑积水。切除囊肿及小脑脑桥角区组织并送至病理科。两例病例的组织病理学表现均显示为囊尾蚴病。

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1
Cysticercosis in the posterior cranial fossa.颅后窝囊尾蚴病
J Med Assoc Thai. 1994 Oct;77(10):544-8.
2
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3
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