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Medical treatment of an unusual cerebral hydatid disease

BACKGROUND: Hydatid disease is a worldwide zoonosis produced by the larval stage of cestodes of the Echinococcus genus. Hydatid disease primarily involves the liver and lungs. The brain is involved in less than 2% of cases. Surgery has long been the only choice for the treatment, but chemotherapy ha...

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Autores principales: Chen, Shu, Li, Ning, Yang, Feifei, Wu, Jiqin, Hu, Yuekai, Yu, Shenglei, Chen, Qi, Wang, Xuan, Wang, Xinyu, Liu, Yuanyuan, Zheng, Jianming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756415/
https://www.ncbi.nlm.nih.gov/pubmed/29304756
http://dx.doi.org/10.1186/s12879-017-2935-2
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author Chen, Shu
Li, Ning
Yang, Feifei
Wu, Jiqin
Hu, Yuekai
Yu, Shenglei
Chen, Qi
Wang, Xuan
Wang, Xinyu
Liu, Yuanyuan
Zheng, Jianming
author_facet Chen, Shu
Li, Ning
Yang, Feifei
Wu, Jiqin
Hu, Yuekai
Yu, Shenglei
Chen, Qi
Wang, Xuan
Wang, Xinyu
Liu, Yuanyuan
Zheng, Jianming
author_sort Chen, Shu
collection PubMed
description BACKGROUND: Hydatid disease is a worldwide zoonosis produced by the larval stage of cestodes of the Echinococcus genus. Hydatid disease primarily involves the liver and lungs. The brain is involved in less than 2% of cases. Surgery has long been the only choice for the treatment, but chemotherapy has been successfully replaced surgery in some special cases. CASE PRESENTATION: We report a rare hydatid disease case which presented with multiple lesions in right frontal lobe, an uncommon site, and in the liver and lungs. A 28-year-old woman presented with 6 months history of recurrent convulsion. Cranial magnetic resonance imaging found multiple lesions in right frontal lobe, so she was hospitalized for surgical treatment and received sodium valproate by oral for controlling epilepsy. Before the operation, other lesions were found in the liver and lungs by computerized tomography scan. There were multiple pulmonary nodules near the pleura and large cyst in the liver. The pathology of liver showed that it may be a hydatid disease. Then, positive serum antibodies for echinococcus antigen further confirmed our diagnosis. Since her central nerve system was involved, she received four pills (800 mg, about 17 mg/kg/day) albendazole treatment for 18 months without operation. Her symptoms abated and a follow-up magnetic resonance imaging showed that the lesion had obviously diminished after treatment. She was recurrence free 2 years after we stopped albendazole treatment. CONCLUSIONS: This case reveals an uncommon pattern of intracranial hydatid disease. Albendazole can be beneficial for some inoperable cerebral hydatid disease patients.
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spelling pubmed-57564152018-01-09 Medical treatment of an unusual cerebral hydatid disease Chen, Shu Li, Ning Yang, Feifei Wu, Jiqin Hu, Yuekai Yu, Shenglei Chen, Qi Wang, Xuan Wang, Xinyu Liu, Yuanyuan Zheng, Jianming BMC Infect Dis Case Report BACKGROUND: Hydatid disease is a worldwide zoonosis produced by the larval stage of cestodes of the Echinococcus genus. Hydatid disease primarily involves the liver and lungs. The brain is involved in less than 2% of cases. Surgery has long been the only choice for the treatment, but chemotherapy has been successfully replaced surgery in some special cases. CASE PRESENTATION: We report a rare hydatid disease case which presented with multiple lesions in right frontal lobe, an uncommon site, and in the liver and lungs. A 28-year-old woman presented with 6 months history of recurrent convulsion. Cranial magnetic resonance imaging found multiple lesions in right frontal lobe, so she was hospitalized for surgical treatment and received sodium valproate by oral for controlling epilepsy. Before the operation, other lesions were found in the liver and lungs by computerized tomography scan. There were multiple pulmonary nodules near the pleura and large cyst in the liver. The pathology of liver showed that it may be a hydatid disease. Then, positive serum antibodies for echinococcus antigen further confirmed our diagnosis. Since her central nerve system was involved, she received four pills (800 mg, about 17 mg/kg/day) albendazole treatment for 18 months without operation. Her symptoms abated and a follow-up magnetic resonance imaging showed that the lesion had obviously diminished after treatment. She was recurrence free 2 years after we stopped albendazole treatment. CONCLUSIONS: This case reveals an uncommon pattern of intracranial hydatid disease. Albendazole can be beneficial for some inoperable cerebral hydatid disease patients. BioMed Central 2018-01-05 /pmc/articles/PMC5756415/ /pubmed/29304756 http://dx.doi.org/10.1186/s12879-017-2935-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Chen, Shu
Li, Ning
Yang, Feifei
Wu, Jiqin
Hu, Yuekai
Yu, Shenglei
Chen, Qi
Wang, Xuan
Wang, Xinyu
Liu, Yuanyuan
Zheng, Jianming
Medical treatment of an unusual cerebral hydatid disease
title Medical treatment of an unusual cerebral hydatid disease
title_full Medical treatment of an unusual cerebral hydatid disease
title_fullStr Medical treatment of an unusual cerebral hydatid disease
title_full_unstemmed Medical treatment of an unusual cerebral hydatid disease
title_short Medical treatment of an unusual cerebral hydatid disease
title_sort medical treatment of an unusual cerebral hydatid disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756415/
https://www.ncbi.nlm.nih.gov/pubmed/29304756
http://dx.doi.org/10.1186/s12879-017-2935-2
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