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Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis
Introduction: Alveolar echinococcosis (AE) is a rare parasitic disease caused by the infection of Echinococcus multilocularis. AE may mimic malignancy both in clinical presentation and radiological imaging, which is often misdiagnosed as metastatic tumor. Recently, next-generation sequencing (NGS) t...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299116/ https://www.ncbi.nlm.nih.gov/pubmed/34306012 http://dx.doi.org/10.3389/fgene.2021.666225 |
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author | Li, Ke Ma, Yubao Ban, Rui Shi, Qiang |
author_facet | Li, Ke Ma, Yubao Ban, Rui Shi, Qiang |
author_sort | Li, Ke |
collection | PubMed |
description | Introduction: Alveolar echinococcosis (AE) is a rare parasitic disease caused by the infection of Echinococcus multilocularis. AE may mimic malignancy both in clinical presentation and radiological imaging, which is often misdiagnosed as metastatic tumor. Recently, next-generation sequencing (NGS) technologies are increasingly being used to address a diverse range of biological questions. Here, we describe a rare case of alveolar echinococcosis diagnosed by pan-pathogen screening, using next-generation sequencing. To the best of our knowledge, this is the first reported case of AE which was definitely diagnosed relying NGS of cerebrospinal fluid (CSF). Case Presentation: A 33-year-old man presented with repeat seizure and progressive headache for six months. Head magnetic resonance imaging (MRI) showed multiple masses with edema. Lung and abdominal computer tomography (CT) revealed multiple masses in bilateral lung, liver and the right adrenal gland. Bacterial, tuberculosis and fungal infection were excluded by CSF examination. Repeated target biopsy on the masses in the lung and liver showed as fibrous connective tissue without positive findings. NGS of CSF was performed and detected nucleic acid sequences of E. multilocularis. Consequently, the patient has accepted 1-year albendazole therapy. His case was followed up through imaging procedures. Conclusion: The next-generation sequencing of CSF is a reliable and sensitive diagnostic method for the detection of pathogenic microorganisms, and may allow the accurate diagnosis of alveolar echinococcosis. In view of this case, we recommend NGS as a potential tool for diagnosis of cerebral AE, especially if repeated biopsies are negative. |
format | Online Article Text |
id | pubmed-8299116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82991162021-07-24 Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis Li, Ke Ma, Yubao Ban, Rui Shi, Qiang Front Genet Genetics Introduction: Alveolar echinococcosis (AE) is a rare parasitic disease caused by the infection of Echinococcus multilocularis. AE may mimic malignancy both in clinical presentation and radiological imaging, which is often misdiagnosed as metastatic tumor. Recently, next-generation sequencing (NGS) technologies are increasingly being used to address a diverse range of biological questions. Here, we describe a rare case of alveolar echinococcosis diagnosed by pan-pathogen screening, using next-generation sequencing. To the best of our knowledge, this is the first reported case of AE which was definitely diagnosed relying NGS of cerebrospinal fluid (CSF). Case Presentation: A 33-year-old man presented with repeat seizure and progressive headache for six months. Head magnetic resonance imaging (MRI) showed multiple masses with edema. Lung and abdominal computer tomography (CT) revealed multiple masses in bilateral lung, liver and the right adrenal gland. Bacterial, tuberculosis and fungal infection were excluded by CSF examination. Repeated target biopsy on the masses in the lung and liver showed as fibrous connective tissue without positive findings. NGS of CSF was performed and detected nucleic acid sequences of E. multilocularis. Consequently, the patient has accepted 1-year albendazole therapy. His case was followed up through imaging procedures. Conclusion: The next-generation sequencing of CSF is a reliable and sensitive diagnostic method for the detection of pathogenic microorganisms, and may allow the accurate diagnosis of alveolar echinococcosis. In view of this case, we recommend NGS as a potential tool for diagnosis of cerebral AE, especially if repeated biopsies are negative. Frontiers Media S.A. 2021-07-09 /pmc/articles/PMC8299116/ /pubmed/34306012 http://dx.doi.org/10.3389/fgene.2021.666225 Text en Copyright © 2021 Li, Ma, Ban and Shi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Li, Ke Ma, Yubao Ban, Rui Shi, Qiang Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis |
title | Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis |
title_full | Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis |
title_fullStr | Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis |
title_full_unstemmed | Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis |
title_short | Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis |
title_sort | case report: diagnosis of human alveolar echinococcosis via next-generation sequencing analysis |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299116/ https://www.ncbi.nlm.nih.gov/pubmed/34306012 http://dx.doi.org/10.3389/fgene.2021.666225 |
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