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Twenty-six years of involvement with cystic echinococcosis: a case report
INTRODUCTION: Spinal hydatidosis, a zoonotic disease caused by infection with Echinococcus spp. larvae, is rare, but its treatment remains a significant medical challenge. Approximately 70% of patients with spinal hydatidosis have lesions in their liver, 0–15% have lung involvement, and only 0.5–2%...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114538/ https://www.ncbi.nlm.nih.gov/pubmed/33980278 http://dx.doi.org/10.1186/s13256-021-02810-9 |
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author | Safari, Hosein Mirzavand, Somayeh Rafiei, Abdollah Beiromvand, Molouk |
author_facet | Safari, Hosein Mirzavand, Somayeh Rafiei, Abdollah Beiromvand, Molouk |
author_sort | Safari, Hosein |
collection | PubMed |
description | INTRODUCTION: Spinal hydatidosis, a zoonotic disease caused by infection with Echinococcus spp. larvae, is rare, but its treatment remains a significant medical challenge. Approximately 70% of patients with spinal hydatidosis have lesions in their liver, 0–15% have lung involvement, and only 0.5–2% have bone involvement. CASE PRESENTATION: Here we report a 38-year-old Iranian man with spinal hydatidosis, who had a history of eight times surgery in over of 26 years due to hydatid cyst in the liver, lungs, and chest wall. At the most recent admission to hospital he presented with chest pain, paraplegia, and urinary incontinence. Magnetic resonance imaging revealed thoracic spinal hydatid disease. He underwent surgery, and the hydatid cysts were completely removed. Lower extremity forces recovered dramatically and completely within 4 weeks. CONCLUSION: Spinal hydatidosis is a rare disease, but it is associated with a high degree of morbidity, mortality, and poor prognosis. Because of the infiltrative nature of hydatid disease, surgery alone is rarely curative. The current case study demonstrates the importance of a suitable surgical approach, adequate intraoperative prophylaxis to prevent cyst rupture, and prolonged complete paraplegia. |
format | Online Article Text |
id | pubmed-8114538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81145382021-05-12 Twenty-six years of involvement with cystic echinococcosis: a case report Safari, Hosein Mirzavand, Somayeh Rafiei, Abdollah Beiromvand, Molouk J Med Case Rep Case Report INTRODUCTION: Spinal hydatidosis, a zoonotic disease caused by infection with Echinococcus spp. larvae, is rare, but its treatment remains a significant medical challenge. Approximately 70% of patients with spinal hydatidosis have lesions in their liver, 0–15% have lung involvement, and only 0.5–2% have bone involvement. CASE PRESENTATION: Here we report a 38-year-old Iranian man with spinal hydatidosis, who had a history of eight times surgery in over of 26 years due to hydatid cyst in the liver, lungs, and chest wall. At the most recent admission to hospital he presented with chest pain, paraplegia, and urinary incontinence. Magnetic resonance imaging revealed thoracic spinal hydatid disease. He underwent surgery, and the hydatid cysts were completely removed. Lower extremity forces recovered dramatically and completely within 4 weeks. CONCLUSION: Spinal hydatidosis is a rare disease, but it is associated with a high degree of morbidity, mortality, and poor prognosis. Because of the infiltrative nature of hydatid disease, surgery alone is rarely curative. The current case study demonstrates the importance of a suitable surgical approach, adequate intraoperative prophylaxis to prevent cyst rupture, and prolonged complete paraplegia. BioMed Central 2021-05-12 /pmc/articles/PMC8114538/ /pubmed/33980278 http://dx.doi.org/10.1186/s13256-021-02810-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Safari, Hosein Mirzavand, Somayeh Rafiei, Abdollah Beiromvand, Molouk Twenty-six years of involvement with cystic echinococcosis: a case report |
title | Twenty-six years of involvement with cystic echinococcosis: a case report |
title_full | Twenty-six years of involvement with cystic echinococcosis: a case report |
title_fullStr | Twenty-six years of involvement with cystic echinococcosis: a case report |
title_full_unstemmed | Twenty-six years of involvement with cystic echinococcosis: a case report |
title_short | Twenty-six years of involvement with cystic echinococcosis: a case report |
title_sort | twenty-six years of involvement with cystic echinococcosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114538/ https://www.ncbi.nlm.nih.gov/pubmed/33980278 http://dx.doi.org/10.1186/s13256-021-02810-9 |
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