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Natural History of Treated Subarachnoid Neurocysticercosis
Subarachnoid neurocysticercosis (SUBNCC) is usually caused by an aberrant proliferative form of Taenia solium causing mass effect and arachnoiditis. Thirty of 34 SUBNCC patients were treated with extended cysticidal and anti-inflammatory regimens and followed up a median of 4.2 years posttreatment (...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society of Tropical Medicine and Hygiene
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947806/ https://www.ncbi.nlm.nih.gov/pubmed/31642423 http://dx.doi.org/10.4269/ajtmh.19-0436 |
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author | Nash, Theodore E. O’Connell, Elise M. Hammoud, Dima A. Wetzler, Lauren Ware, JeanAnne M. Mahanty, Siddhartha |
author_facet | Nash, Theodore E. O’Connell, Elise M. Hammoud, Dima A. Wetzler, Lauren Ware, JeanAnne M. Mahanty, Siddhartha |
author_sort | Nash, Theodore E. |
collection | PubMed |
description | Subarachnoid neurocysticercosis (SUBNCC) is usually caused by an aberrant proliferative form of Taenia solium causing mass effect and arachnoiditis. Thirty of 34 SUBNCC patients were treated with extended cysticidal and anti-inflammatory regimens and followed up a median of 4.2 years posttreatment (range: 15 for ≥ 4 years, 20 ≥ 2 years, 26 > 1 year, and 3 < 1 year). The median ages at the time of first symptom, diagnosis, and enrollment were 29.7, 35.6, and 37.9 years, respectively; 58.8% were male and 82.4% were Hispanic. The median time from immigration to symptoms (minimum incubation) was 10 years and the estimated true incubation period considerably greater. Fifty percent also had other forms of NCC. Common complications were hydrocephalus (56%), shunt placement (41%), infarcts (18%), and symptomatic spinal disease (15%). Thirty patients (88.2%) required prolonged treatment with albendazole (88.2%, median 0.55 year) and/or praziquantel (61.8%; median 0.96 year), corticosteroids (88.2%, median 1.09 years), methotrexate (50%, median 1.37 years), and etanercept (34.2%, median 0.81 year), which led to sustained inactive disease in 29/30 (96.7%) patients. Three were treated successfully for recurrences and one has continuing infection. Normalization of cerebral spinal fluid parameters and cestode antigen levels guided treatment decisions. All 15 patients with undetectable cestode antigen values have sustained inactive disease. There were no deaths and moderate morbidity posttreatment. Corticosteroid-related side effects were common, avascular necrosis of joints being the most serious (8/33, 24.2%). Prolonged cysticidal treatment and effective control of inflammation led to good clinical outcomes and sustained inactive disease which is likely curative. |
format | Online Article Text |
id | pubmed-6947806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society of Tropical Medicine and Hygiene |
record_format | MEDLINE/PubMed |
spelling | pubmed-69478062020-01-27 Natural History of Treated Subarachnoid Neurocysticercosis Nash, Theodore E. O’Connell, Elise M. Hammoud, Dima A. Wetzler, Lauren Ware, JeanAnne M. Mahanty, Siddhartha Am J Trop Med Hyg Articles Subarachnoid neurocysticercosis (SUBNCC) is usually caused by an aberrant proliferative form of Taenia solium causing mass effect and arachnoiditis. Thirty of 34 SUBNCC patients were treated with extended cysticidal and anti-inflammatory regimens and followed up a median of 4.2 years posttreatment (range: 15 for ≥ 4 years, 20 ≥ 2 years, 26 > 1 year, and 3 < 1 year). The median ages at the time of first symptom, diagnosis, and enrollment were 29.7, 35.6, and 37.9 years, respectively; 58.8% were male and 82.4% were Hispanic. The median time from immigration to symptoms (minimum incubation) was 10 years and the estimated true incubation period considerably greater. Fifty percent also had other forms of NCC. Common complications were hydrocephalus (56%), shunt placement (41%), infarcts (18%), and symptomatic spinal disease (15%). Thirty patients (88.2%) required prolonged treatment with albendazole (88.2%, median 0.55 year) and/or praziquantel (61.8%; median 0.96 year), corticosteroids (88.2%, median 1.09 years), methotrexate (50%, median 1.37 years), and etanercept (34.2%, median 0.81 year), which led to sustained inactive disease in 29/30 (96.7%) patients. Three were treated successfully for recurrences and one has continuing infection. Normalization of cerebral spinal fluid parameters and cestode antigen levels guided treatment decisions. All 15 patients with undetectable cestode antigen values have sustained inactive disease. There were no deaths and moderate morbidity posttreatment. Corticosteroid-related side effects were common, avascular necrosis of joints being the most serious (8/33, 24.2%). Prolonged cysticidal treatment and effective control of inflammation led to good clinical outcomes and sustained inactive disease which is likely curative. The American Society of Tropical Medicine and Hygiene 2020-01 2019-10-21 /pmc/articles/PMC6947806/ /pubmed/31642423 http://dx.doi.org/10.4269/ajtmh.19-0436 Text en © The American Society of Tropical Medicine and Hygiene This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Articles Nash, Theodore E. O’Connell, Elise M. Hammoud, Dima A. Wetzler, Lauren Ware, JeanAnne M. Mahanty, Siddhartha Natural History of Treated Subarachnoid Neurocysticercosis |
title | Natural History of Treated Subarachnoid Neurocysticercosis |
title_full | Natural History of Treated Subarachnoid Neurocysticercosis |
title_fullStr | Natural History of Treated Subarachnoid Neurocysticercosis |
title_full_unstemmed | Natural History of Treated Subarachnoid Neurocysticercosis |
title_short | Natural History of Treated Subarachnoid Neurocysticercosis |
title_sort | natural history of treated subarachnoid neurocysticercosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947806/ https://www.ncbi.nlm.nih.gov/pubmed/31642423 http://dx.doi.org/10.4269/ajtmh.19-0436 |
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