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dc.contributor.author | Boggild, A.K. | |
dc.contributor.author | Valencia, B.M. | |
dc.contributor.author | Veland, N. | |
dc.contributor.author | Ramos, A.P. | |
dc.contributor.author | Calderon, F. | |
dc.contributor.author | Arévalo Zelada, Jorge Luis | |
dc.contributor.author | Low, D.E. | |
dc.contributor.author | Llanos Cuentas, Elmer Alejandro | |
dc.date.accessioned | 2022-01-18T19:34:39Z | |
dc.date.available | 2022-01-18T19:34:39Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/11094 | |
dc.description.abstract | Background: Traditional methods of diagnosing mucosal leishmaniasis (ML), such as biopsy with histopathology, are insensitive and require collection of an invasive diagnostic specimen. Methods: We compared standard invasive procedures including biopsy histopathology, biopsy PCR, and leishmanin skin test (LST) to a novel, non-invasive, cytology-brush based PCR for the diagnosis of ML in Lima, Peru. Consensus reference standard was 2/4 tests positive, and outcome measures were sensitivity and specificity. Leishmania species identification was performed by PCR-based assays of positive specimens. Results: Twenty-eight patients were enrolled, 23 of whom fulfilled criteria for a diagnosis of ML. Sensitivity and specificity of biopsy with histopathology were 21.7% [95% CI 4.9-38.5%] and 100%; 69.6% [95% CI 50.8-88.4%] and 100% for LST; 95.7% [95% CI 87.4-100%] and 100% for biopsy PCR; and 95.7% [95% CI 87.4-100%] and 90% [95% CI 71.4-100%] for cytology brush PCR using both Cervisoft® and Histobrush® cervical cytology brushes. Represented species identified by PCR-RFLP included: L. (V). braziliensis (n = 4), and L. (V). peruviana (n = 3). Conclusions: Use of commercial grade cytology brush PCR for diagnosis of ML is sensitive, rapid, well tolerated, and carries none of the risks of invasive diagnostic procedures such as biopsy. Further optimization is required for adequate species identification. Further evaluation of this method in field and other settings is warranted. | en_US |
dc.language.iso | eng | |
dc.publisher | Public Library of Science | |
dc.relation.ispartofseries | PLoS ONE | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | Humans | en_US |
dc.subject | Peru | en_US |
dc.subject | Biopsy | en_US |
dc.subject | comparative study | en_US |
dc.subject | controlled study | en_US |
dc.subject | human tissue | en_US |
dc.subject | nose mucosa | en_US |
dc.subject | polymerase chain reaction | en_US |
dc.subject | methodology | en_US |
dc.subject | clinical article | en_US |
dc.subject | Leishmania braziliensis | en_US |
dc.subject | Polymerase Chain Reaction | en_US |
dc.subject | skin leishmaniasis | en_US |
dc.subject | histopathology | en_US |
dc.subject | molecular diagnosis | en_US |
dc.subject | Sensitivity and Specificity | en_US |
dc.subject | cytology | en_US |
dc.subject | parasite identification | en_US |
dc.subject | diagnostic test accuracy study | en_US |
dc.subject | standard | en_US |
dc.subject | controlled clinical trial | en_US |
dc.subject | restriction fragment length polymorphism | en_US |
dc.subject | Leishmania | en_US |
dc.subject | Leishmania lainsoni | en_US |
dc.subject | leishmaniasis | en_US |
dc.subject | clinical trial | en_US |
dc.subject | intermethod comparison | en_US |
dc.subject | leishmania peruviana | en_US |
dc.subject | Leishmaniasis, Mucocutaneous | en_US |
dc.subject | Skin Tests | en_US |
dc.subject | mouth mucosa | en_US |
dc.subject | uterine cervix cytology | en_US |
dc.subject | Molecular Diagnostic Techniques | en_US |
dc.subject | non invasive measurement | en_US |
dc.subject | instrumentation | en_US |
dc.subject | cheek mucosa | en_US |
dc.subject | mucosal leishmaniasis | en_US |
dc.subject | pharynx | en_US |
dc.title | Non-invasive cytology brush pcr diagnostic testing in mucosal leishmaniasis: Superior performance to conventional biopsy with histopathology | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1371/journal.pone.0026395 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.01.00 | |
dc.relation.issn | 1932-6203 |
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