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Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model

Chronic endometritis (CE) is a localized mucosal infectious and inflammatory disorder marked by infiltration of CD138(+) endometrial stromal plasmacytes (ESPC). CE is drawing interest in the field of reproductive medicine because of its association with female infertility of unknown etiology, endome...

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Autores principales: Mihara, Masaya, Yasuo, Tadahiro, Kitaya, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000436/
https://www.ncbi.nlm.nih.gov/pubmed/36900079
http://dx.doi.org/10.3390/diagnostics13050936
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author Mihara, Masaya
Yasuo, Tadahiro
Kitaya, Kotaro
author_facet Mihara, Masaya
Yasuo, Tadahiro
Kitaya, Kotaro
author_sort Mihara, Masaya
collection PubMed
description Chronic endometritis (CE) is a localized mucosal infectious and inflammatory disorder marked by infiltration of CD138(+) endometrial stromal plasmacytes (ESPC). CE is drawing interest in the field of reproductive medicine because of its association with female infertility of unknown etiology, endometriosis, repeated implantation failure, recurrent pregnancy loss, and multiple maternal/newborn complications. The diagnosis of CE has long relied on somewhat painful endometrial biopsy and histopathologic examinations combined with immunohistochemistry for CD138 (IHC-CD138). With IHC-CD138 only, CE may be potentially over-diagnosed by misidentification of endometrial epithelial cells, which constitutively express CD138, as ESPCs. Fluid hysteroscopy is emerging as an alternative, less-invasive diagnostic tool that can visualize the whole uterine cavity in real-time and enables the detection of several unique mucosal findings associated with CE. The biases in the hysteroscopic diagnosis of CE; however, are the inter-observer and intra-observer disagreements on the interpretation of the endoscopic findings. Additionally, due to the variances in the study designs and adopted diagnostic criteria, there exists some dissociation in the histopathologic and hysteroscopic diagnosis of CE among researchers. To address these questions, novel dual immunohistochemistry for CD138 and another plasmacyte marker multiple myeloma oncogene 1 are currently being tested. Furthermore, computer-aided diagnosis using a deep learning model is being developed for more accurate detection of ESPCs. These approaches have the potential to contribute to the reduction in human errors and biases, the improvement of the diagnostic performance of CE, and the establishment of unified diagnostic criteria and standardized clinical guidelines for the disease.
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spelling pubmed-100004362023-03-11 Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model Mihara, Masaya Yasuo, Tadahiro Kitaya, Kotaro Diagnostics (Basel) Review Chronic endometritis (CE) is a localized mucosal infectious and inflammatory disorder marked by infiltration of CD138(+) endometrial stromal plasmacytes (ESPC). CE is drawing interest in the field of reproductive medicine because of its association with female infertility of unknown etiology, endometriosis, repeated implantation failure, recurrent pregnancy loss, and multiple maternal/newborn complications. The diagnosis of CE has long relied on somewhat painful endometrial biopsy and histopathologic examinations combined with immunohistochemistry for CD138 (IHC-CD138). With IHC-CD138 only, CE may be potentially over-diagnosed by misidentification of endometrial epithelial cells, which constitutively express CD138, as ESPCs. Fluid hysteroscopy is emerging as an alternative, less-invasive diagnostic tool that can visualize the whole uterine cavity in real-time and enables the detection of several unique mucosal findings associated with CE. The biases in the hysteroscopic diagnosis of CE; however, are the inter-observer and intra-observer disagreements on the interpretation of the endoscopic findings. Additionally, due to the variances in the study designs and adopted diagnostic criteria, there exists some dissociation in the histopathologic and hysteroscopic diagnosis of CE among researchers. To address these questions, novel dual immunohistochemistry for CD138 and another plasmacyte marker multiple myeloma oncogene 1 are currently being tested. Furthermore, computer-aided diagnosis using a deep learning model is being developed for more accurate detection of ESPCs. These approaches have the potential to contribute to the reduction in human errors and biases, the improvement of the diagnostic performance of CE, and the establishment of unified diagnostic criteria and standardized clinical guidelines for the disease. MDPI 2023-03-01 /pmc/articles/PMC10000436/ /pubmed/36900079 http://dx.doi.org/10.3390/diagnostics13050936 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mihara, Masaya
Yasuo, Tadahiro
Kitaya, Kotaro
Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model
title Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model
title_full Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model
title_fullStr Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model
title_full_unstemmed Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model
title_short Precision Medicine for Chronic Endometritis: Computer-Aided Diagnosis Using Deep Learning Model
title_sort precision medicine for chronic endometritis: computer-aided diagnosis using deep learning model
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000436/
https://www.ncbi.nlm.nih.gov/pubmed/36900079
http://dx.doi.org/10.3390/diagnostics13050936
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