Terada K, Seno K, Uetsuhara K, Asakura T
Department of Neurosurgery, Oshima Prefectural Hospital, Kagoshima.
No Shinkei Geka. 1990 Apr;18(4):391-5.
A rare case of a 40-year-old woman with cerebral cysticercosis is reported. She has lived on the Island of Tokunoshima and has never travelled overseas. She was hospitalized in the hospital of Kagoshima University in 1980. A small cyst in the right temporal lobe, and a calcified area in the left parietal lobe was noticed on CT scan. When she was admitted to our hospital in December 1986, the cyst in the right temporal lobe was larger than it was 6 years before. An operation was performed for the cyst in the right temporal lobe. The cyst was pathologically confirmed as cysticercosis. Postoperatively, immunological reaction of cysticercosis was positive, but X-rays and CT scan of extremities showed no abnormal findings. Cerebral cysticercosis is a rare disease in Japan. CT scan is very useful in the diagnosis of this disease. Multiple cysts and calcified area in the parenchymal region are specific findings on CT scan.
报告了一例40岁脑囊尾蚴病女性的罕见病例。她生活在德之岛,从未出过国。1980年她在鹿儿岛大学医院住院。CT扫描发现右侧颞叶有一个小囊肿,左侧顶叶有一个钙化区。1986年12月她入住我院时,右侧颞叶的囊肿比6年前更大。对右侧颞叶的囊肿进行了手术。囊肿经病理证实为囊尾蚴病。术后,囊尾蚴病的免疫反应呈阳性,但四肢的X线和CT扫描未发现异常。脑囊尾蚴病在日本是一种罕见疾病。CT扫描对该病的诊断非常有用。实质区域的多个囊肿和钙化区是CT扫描的特异性表现。