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肝囊尾蚴病。1例罕见病例报告。

Hepatic cysticercosis. Report of an unusual case.

作者信息

Sickel J Z, Fultz P J, Penwarden B, Laczin J

机构信息

Department of Pathology, University of Rochester Medical Center, NY 14627, USA.

出版信息

J Clin Gastroenterol. 1995 Mar;20(2):160-3.

PMID:7769202
Abstract

We report a case of hepatic cysticercosis in a 62-year-old man who had been diagnosed with a colonic adenocarcinoma 9 years previously. Additional clinical studies failed to show disease in the soft tissues, brain, orbit and heart. The patient was successfully treated with a course of praziquantel and prednisone and is alive and well 28 months after diagnosis. This is the first reported case of hepatic cysticercosis that has resulted in significant morbidity.

摘要

我们报告一例62岁男性肝囊尾蚴病患者,该患者9年前被诊断为结肠腺癌。进一步的临床检查未发现软组织、脑、眼眶及心脏有病变。患者接受了一个疗程的吡喹酮和泼尼松治疗,治疗成功,诊断后28个月仍存活且情况良好。这是首例有显著发病率的肝囊尾蚴病报告病例。

相似文献

1
Hepatic cysticercosis. Report of an unusual case.肝囊尾蚴病。1例罕见病例报告。
J Clin Gastroenterol. 1995 Mar;20(2):160-3.
2
Hepatic cysticercosis: a rare entity.肝囊尾蚴病:一种罕见病症。
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[Epilepsy, intracranial hypertension, confusional syndrome and cutaneous cysticercosis. Apropos of 1 case observed in a hospital in Benin].[癫痫、颅内高压、意识模糊综合征与皮肤囊尾蚴病。关于在贝宁一家医院观察到的1例病例]
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Isolated cysticercosis of the liver - A rare case report on diagnosis and management of an incidental finding during prepyloric perforation peritonitis repair.孤立性肝囊尾蚴病——关于胃幽门穿孔性腹膜炎修补术中偶然发现的诊断与处理的罕见病例报告
Trop Parasitol. 2024 Jul-Dec;14(2):120-123. doi: 10.4103/tp.tp_62_23. Epub 2024 Sep 3.
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Disseminated cysticercosis: rare manifestation of a common disease.
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