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Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis

BACKGROUND: The gold standard for the diagnosis of schistosomiasis is the detection of the parasite's characteristic eggs in urine, stool, or rectal and bladder biopsy specimens. Direct detection of eggs is difficult and not always possible in patients with low egg-shedding rates. Confocal lase...

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Autores principales: Fritzsche, Carlos, Stachs, Oliver, Holtfreter, Martha Charlotte, Nohr-Łuczak, Constanze, Guthoff, Rudolf Friedrich, Reisinger, Emil Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328486/
https://www.ncbi.nlm.nih.gov/pubmed/22529947
http://dx.doi.org/10.1371/journal.pone.0034869
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author Fritzsche, Carlos
Stachs, Oliver
Holtfreter, Martha Charlotte
Nohr-Łuczak, Constanze
Guthoff, Rudolf Friedrich
Reisinger, Emil Christian
author_facet Fritzsche, Carlos
Stachs, Oliver
Holtfreter, Martha Charlotte
Nohr-Łuczak, Constanze
Guthoff, Rudolf Friedrich
Reisinger, Emil Christian
author_sort Fritzsche, Carlos
collection PubMed
description BACKGROUND: The gold standard for the diagnosis of schistosomiasis is the detection of the parasite's characteristic eggs in urine, stool, or rectal and bladder biopsy specimens. Direct detection of eggs is difficult and not always possible in patients with low egg-shedding rates. Confocal laser scanning microscopy (CLSM) permits non-invasive cell imaging in vivo and is an established way of obtaining high-resolution images and 3-dimensional reconstructions. Recently, CLSM was shown to be a suitable method to visualize Schistosoma mansoni eggs within the mucosa of dissected mouse gut. In this case, we evaluated the suitability of CLSM to detect eggs of Schistosoma haematobium in a patient with urinary schistosomiasis and low egg-shedding rates. METHODOLOGY/PRINCIPAL FINDINGS: The confocal laser scanning microscope used in this study was based on a scanning laser system for imaging the retina of a living eye, the Heidelberg Retina Tomograph II, in combination with a lens system (image modality). Standard light cystoscopy was performed using a rigid cystoscope under general anaesthesia. The CLSM endoscope was then passed through the working channel of the rigid cystoscope. The mucosal tissue of the bladder was scanned using CLSM. Schistoma haematobium eggs appeared as bright structures, with the characteristic egg shape and typical terminal spine. CONCLUSION/SIGNIFICANCE: We were able to detect schistosomal eggs in the urothelium of a patient with urinary schistosomiasis. Thus, CLSM may be a suitable tool for the diagnosis of schistosomiasis in humans, especially in cases where standard diagnostic tools are not suitable.
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spelling pubmed-33284862012-04-23 Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis Fritzsche, Carlos Stachs, Oliver Holtfreter, Martha Charlotte Nohr-Łuczak, Constanze Guthoff, Rudolf Friedrich Reisinger, Emil Christian PLoS One Research Article BACKGROUND: The gold standard for the diagnosis of schistosomiasis is the detection of the parasite's characteristic eggs in urine, stool, or rectal and bladder biopsy specimens. Direct detection of eggs is difficult and not always possible in patients with low egg-shedding rates. Confocal laser scanning microscopy (CLSM) permits non-invasive cell imaging in vivo and is an established way of obtaining high-resolution images and 3-dimensional reconstructions. Recently, CLSM was shown to be a suitable method to visualize Schistosoma mansoni eggs within the mucosa of dissected mouse gut. In this case, we evaluated the suitability of CLSM to detect eggs of Schistosoma haematobium in a patient with urinary schistosomiasis and low egg-shedding rates. METHODOLOGY/PRINCIPAL FINDINGS: The confocal laser scanning microscope used in this study was based on a scanning laser system for imaging the retina of a living eye, the Heidelberg Retina Tomograph II, in combination with a lens system (image modality). Standard light cystoscopy was performed using a rigid cystoscope under general anaesthesia. The CLSM endoscope was then passed through the working channel of the rigid cystoscope. The mucosal tissue of the bladder was scanned using CLSM. Schistoma haematobium eggs appeared as bright structures, with the characteristic egg shape and typical terminal spine. CONCLUSION/SIGNIFICANCE: We were able to detect schistosomal eggs in the urothelium of a patient with urinary schistosomiasis. Thus, CLSM may be a suitable tool for the diagnosis of schistosomiasis in humans, especially in cases where standard diagnostic tools are not suitable. Public Library of Science 2012-04-17 /pmc/articles/PMC3328486/ /pubmed/22529947 http://dx.doi.org/10.1371/journal.pone.0034869 Text en Fritzsche et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fritzsche, Carlos
Stachs, Oliver
Holtfreter, Martha Charlotte
Nohr-Łuczak, Constanze
Guthoff, Rudolf Friedrich
Reisinger, Emil Christian
Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis
title Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis
title_full Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis
title_fullStr Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis
title_full_unstemmed Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis
title_short Confocal Laser Scanning Microscopy, a New In Vivo Diagnostic Tool for Schistosomiasis
title_sort confocal laser scanning microscopy, a new in vivo diagnostic tool for schistosomiasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328486/
https://www.ncbi.nlm.nih.gov/pubmed/22529947
http://dx.doi.org/10.1371/journal.pone.0034869
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