Shimizu Y, Kagawa S, Onuma T
No Shinkei Geka. 1986 Feb;14(2):209-13.
A rare case of cerebral cysticercosis is reported. The patient, a 49-year-old man, had been to Central America several times since 1963. He had an episode of seizure in March 1980 and again in August 1983, and was admitted to our hospital. Skull X-ray, cerebral angiography, scintigraphy, EEG, CSF examination, Chest X-ray, blood and urine examinations were all normal. CT scan only revealed a small lesion in the left frontal lobe as a well circumscribed round low density area with ring-like enhancement. An operation was performed for a suspected brain tumor. However, a cyst was found in the left frontal lobe and was totally extirpated. The microscopic examination revealed a scolex, hooks, and a cyst characteristic of cysticercosis. Postoperative examinations, X-ray of extremities, abdominal CT and immunological reactions of cysticercosis showed no abnormal findings. Cerebral cysticercosis, a rare disease in Japan, may increase proportionally with the increase of world travel. In this case, CT scan was useful for the diagnosis of cysticercosis.
报告了一例罕见的脑囊尾蚴病病例。患者为一名49岁男性,自1963年以来曾多次前往中美洲。他在1980年3月和1983年8月各有一次癫痫发作,随后入院。头颅X线、脑血管造影、闪烁扫描、脑电图、脑脊液检查、胸部X线、血液和尿液检查均正常。CT扫描仅显示左额叶有一个小病变,为边界清晰的圆形低密度区,有环状强化。因怀疑为脑肿瘤而进行了手术。然而,在左额叶发现了一个囊肿并将其完全切除。显微镜检查发现有一个头节、小钩以及具有囊尾蚴病特征的囊肿。术后检查,包括四肢X线、腹部CT和囊尾蚴病免疫反应均未发现异常。脑囊尾蚴病在日本是一种罕见疾病,其发病率可能会随着全球旅行的增加而成比例上升。在本病例中,CT扫描对囊尾蚴病的诊断很有用。