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Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings
BACKGROUND: Neurocysticercosis (NCC) is common in eastern Africa, but disease presentation varies considerably. Most patients have single or few NCC-typical lesions in their brain but some present with a large number of lesions. We present three patients with positive antibody-based serology for Tae...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324188/ https://www.ncbi.nlm.nih.gov/pubmed/37408061 http://dx.doi.org/10.1186/s13256-023-03974-2 |
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author | Stelzle, D. Makasi, C. Welte, T. M. Ruether, C. Schmidt, V. Gabriel, S. Bottieau, E. Fleury, A. Ngowi, B. J. Winkler, A. S. |
author_facet | Stelzle, D. Makasi, C. Welte, T. M. Ruether, C. Schmidt, V. Gabriel, S. Bottieau, E. Fleury, A. Ngowi, B. J. Winkler, A. S. |
author_sort | Stelzle, D. |
collection | PubMed |
description | BACKGROUND: Neurocysticercosis (NCC) is common in eastern Africa, but disease presentation varies considerably. Most patients have single or few NCC-typical lesions in their brain but some present with a large number of lesions. We present three patients with positive antibody-based serology for Taenia solium cysticercosis screened at the Vwawa district hospital, Mbozi district, southern Tanzania, in whom extensive NCC was confirmed by neuroimaging. CASE PRESENTATIONS: Patient 1 was a 55-year-old female from the tribe Malila smallholder farmer who has had four generalized tonic–clonic epileptic seizures over a period of 11 years and one episode of transient left hemiparesis one year before seizure onset. The patient also reported monthly to weekly episodes of severe, progressive, unilateral headache. The computed tomography (CT) scan of the brain showed 25 NCC lesions of which 15 were in the vesicular stage. Patient 2 was a 30-year-old male from tribe Nyha mechanic who reported monthly episodes of moderate to severe, progressive, bilateral headache, but no epileptic seizures. The CT scan showed 63 NCC lesions of which 50 were in the vesicular stage. Patient 3 was a 54-year-old female from the tribe Malila smallholder farmer who suffered from frequent generalized tonic–clonic epileptic seizures with potential signs of focal seizure onset. She also reported weekly to daily episodes of severe, progressive, unilateral headache. The CT scan showed 29 NCC lesions of which 28 were in the vesicular stage. CONCLUSIONS: Clinical presentation of NCC with multiple brain lesions varies considerably ranging from few epileptic seizures and severe headache to severe epilepsy with frequent epileptic seizures. Individuals with neurological signs/symptoms that may be due to NCC, based for example on epidemiological criteria or serological evidence of cysticercosis, are recommended to undergo neuroimaging before anthelminthic treatment is considered. |
format | Online Article Text |
id | pubmed-10324188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103241882023-07-07 Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings Stelzle, D. Makasi, C. Welte, T. M. Ruether, C. Schmidt, V. Gabriel, S. Bottieau, E. Fleury, A. Ngowi, B. J. Winkler, A. S. J Med Case Rep Case Report BACKGROUND: Neurocysticercosis (NCC) is common in eastern Africa, but disease presentation varies considerably. Most patients have single or few NCC-typical lesions in their brain but some present with a large number of lesions. We present three patients with positive antibody-based serology for Taenia solium cysticercosis screened at the Vwawa district hospital, Mbozi district, southern Tanzania, in whom extensive NCC was confirmed by neuroimaging. CASE PRESENTATIONS: Patient 1 was a 55-year-old female from the tribe Malila smallholder farmer who has had four generalized tonic–clonic epileptic seizures over a period of 11 years and one episode of transient left hemiparesis one year before seizure onset. The patient also reported monthly to weekly episodes of severe, progressive, unilateral headache. The computed tomography (CT) scan of the brain showed 25 NCC lesions of which 15 were in the vesicular stage. Patient 2 was a 30-year-old male from tribe Nyha mechanic who reported monthly episodes of moderate to severe, progressive, bilateral headache, but no epileptic seizures. The CT scan showed 63 NCC lesions of which 50 were in the vesicular stage. Patient 3 was a 54-year-old female from the tribe Malila smallholder farmer who suffered from frequent generalized tonic–clonic epileptic seizures with potential signs of focal seizure onset. She also reported weekly to daily episodes of severe, progressive, unilateral headache. The CT scan showed 29 NCC lesions of which 28 were in the vesicular stage. CONCLUSIONS: Clinical presentation of NCC with multiple brain lesions varies considerably ranging from few epileptic seizures and severe headache to severe epilepsy with frequent epileptic seizures. Individuals with neurological signs/symptoms that may be due to NCC, based for example on epidemiological criteria or serological evidence of cysticercosis, are recommended to undergo neuroimaging before anthelminthic treatment is considered. BioMed Central 2023-07-06 /pmc/articles/PMC10324188/ /pubmed/37408061 http://dx.doi.org/10.1186/s13256-023-03974-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Stelzle, D. Makasi, C. Welte, T. M. Ruether, C. Schmidt, V. Gabriel, S. Bottieau, E. Fleury, A. Ngowi, B. J. Winkler, A. S. Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings |
title | Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings |
title_full | Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings |
title_fullStr | Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings |
title_full_unstemmed | Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings |
title_short | Report of three patients with extensive neurocysticercosis in rural southern Tanzania: neurological, serological and neuroradiological findings |
title_sort | report of three patients with extensive neurocysticercosis in rural southern tanzania: neurological, serological and neuroradiological findings |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324188/ https://www.ncbi.nlm.nih.gov/pubmed/37408061 http://dx.doi.org/10.1186/s13256-023-03974-2 |
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