Sugiyama M, Okada T, Higuchi H, Yabe Y, Kobayashi N, Teramoto A
Department of Neurosurgery, Ebina General Hospital East, Japan.
No Shinkei Geka. 2000 Sep;28(9):807-10.
In Japan neurocysticercosis is a rare disease. We report a case of neurocysticercosis with a review of the literature. A 29-year-old man presented focal seizure on the left side. Physical and neurological findings on admission were unremarkable. CT and MRI showed a mass with ring-like enhancement and perifocal edema in the right frontal lobe, as well as multiple small masses with calcification. The main mass measuring 8 mm in diameter, was suspected as the eliptogenic focus, and was totally removed via the transcortical approach. Postsurgically seizures did not recur, and histological examination of the mass confirmed a cysticercus. A therapeutic course of albendazole and praziquantel administered postsurgically was effective for the multiple intraparenchymal masses.
在日本,神经囊尾蚴病是一种罕见疾病。我们报告一例神经囊尾蚴病病例并对文献进行综述。一名29岁男性出现左侧局灶性癫痫发作。入院时体格检查和神经系统检查未发现异常。CT和MRI显示右额叶有一个环状强化伴灶周水肿的肿块,以及多个有钙化的小肿块。直径8毫米的主要肿块被怀疑为致痫灶,通过经皮质入路将其完全切除。术后癫痫未复发,肿块的组织学检查证实为囊尾蚴。术后给予阿苯达唑和吡喹酮的治疗疗程对多个脑实质内肿块有效。