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Evaluating a Semi-Nested Pcr to Support Histopathology Reports of Fungal Rhinosinusitis in Formalin-Fixed Paraffin-Embedded Tissue Samples Publisher Pubmed



Ashraf MJ1 ; Kord M2 ; Morovati H2 ; Ansari S3 ; Shekarkhar G1 ; Badali H4, 5 ; Pakshir K2, 6 ; Shamsizadeh F2 ; Khademi B7, 8 ; Shishegar M7, 8 ; Ahmadikia K9 ; Zomorodian K2, 6
Authors
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Authors Affiliations
  1. 1. Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  2. 2. Department of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  3. 3. Department of Medical Parasitology and Mycology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  4. 4. Fungus Testing Laboratory, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, United States
  5. 5. Invasive Fungi Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran
  6. 6. Basic Sciences in Infectious Diseases Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  7. 7. Research Center of Otolaryngology Head and Neck Surgery, Shiraz University of Medical Sciences, Shiraz, Iran
  8. 8. Department of Otolaryngology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  9. 9. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Clinical Laboratory Analysis Published:2022


Abstract

Background: Fungal rhinosinusitis (FRS) encompasses a various spectrum of diseases. Histopathology is the “reference method” for diagnosing FRS, but it cannot determine the genus and species. Moreover, in more than 50% of the histopathologically proven cases, the culture elicited no reliable results. This study was an attempt to evaluate the diagnostic efficiency of semi-nested polymerase chain reaction (PCR) from formalin-fixed paraffin-embedded (FFPE) functional endoscopic sinus surgery (FESS) in FRS patients. Methods: One hundred ten specimens were subjected to DNA extraction and histopathology examination. The amplification of the β-globin gene by conventional PCR was used to confirm the quality of extracted DNA. The semi-nested PCR was performed using ITS1, ITS2, and ITS4 primers during two steps. Sequencing the internal transcribed spacer region (ITS1-5.8S-ITS2) to identify causative agents was performed on PCR products. Results: Sixty-four out of 110 samples were positive by histopathology evidence, of which 56 samples (87.5%) were positive by PCR. Out of 46 negative samples by histopathological methods, five samples (10.9%) yielded positive results by PCR. Sensitivity, specificity, positive predictive value, and negative predictive value of the semi-nested PCR method were reported 87.5%, 89.2%, 92.7%, and 85.2%, respectively. The kappa factor between PCR and histopathological methods was 0.76, indicating substantial agreements between these two tests. Conclusion: Due to the acceptable sensitivity and specificity of the present method, it might be used to diagnose fungal sinusitis infections along with microscopic techniques. This method is recommended to confirm the diagnose of suspected fungal sinusitis with negative histopathology results. © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.