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Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015

For canine mast cell tumour (MCT), histopathology reports are one of the main factors considered in the decision‐making process regarding need and type of adjunctive therapy. However, considerable variation exists in types of information reported, especially relating to surgical margins. The purpose...

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Autores principales: Reagan, Jennifer K., Selmic, Laura E., Fallon, Caroline, Driskell, Elizabeth A., Garrett, Laura D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090413/
https://www.ncbi.nlm.nih.gov/pubmed/29877634
http://dx.doi.org/10.1002/vms3.107
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author Reagan, Jennifer K.
Selmic, Laura E.
Fallon, Caroline
Driskell, Elizabeth A.
Garrett, Laura D.
author_facet Reagan, Jennifer K.
Selmic, Laura E.
Fallon, Caroline
Driskell, Elizabeth A.
Garrett, Laura D.
author_sort Reagan, Jennifer K.
collection PubMed
description For canine mast cell tumour (MCT), histopathology reports are one of the main factors considered in the decision‐making process regarding need and type of adjunctive therapy. However, considerable variation exists in types of information reported, especially relating to surgical margins. The purpose of this study was to describe and evaluate how information is presented within canine MCT histopathology reports across the United States. The reports were collected from medical and surgical oncologists from 4 geographic regions of the USA: Midwest, Northeast, South and West. All reports were obtained between January 1st 2012 and May 1st 2015. Inclusion criteria required that the final diagnosis was MCT, a microscopic description was present, and it was not a scar revision. Three hundred and sixty‐eight reports were collected from 26 contributors. While the majority of the reports contained a clinical history (85.9%), information for certain prognostic indicators such as location and mass size was lacking. Grading with both Patnaik and Kiupel systems were described in 76.5% of reports with a single system being used in 7.1% and 15.2% of reports, respectively. Subcutaneous MCT were assigned a grading scheme in 67.2% of reports with 33.3% stating appropriate limitations. Surgical margins were reported in 92% of the reports with 77.2% describing deep and lateral margins separately. Tissue composing the deep margin was only described in 10.9% of the reports. The present results indicate reporting of MCT has variability across pathologists with inconsistencies present in the reporting of clinical history, margin evaluation and subcutaneous MCT grading.
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spelling pubmed-60904132018-08-17 Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015 Reagan, Jennifer K. Selmic, Laura E. Fallon, Caroline Driskell, Elizabeth A. Garrett, Laura D. Vet Med Sci Original Articles For canine mast cell tumour (MCT), histopathology reports are one of the main factors considered in the decision‐making process regarding need and type of adjunctive therapy. However, considerable variation exists in types of information reported, especially relating to surgical margins. The purpose of this study was to describe and evaluate how information is presented within canine MCT histopathology reports across the United States. The reports were collected from medical and surgical oncologists from 4 geographic regions of the USA: Midwest, Northeast, South and West. All reports were obtained between January 1st 2012 and May 1st 2015. Inclusion criteria required that the final diagnosis was MCT, a microscopic description was present, and it was not a scar revision. Three hundred and sixty‐eight reports were collected from 26 contributors. While the majority of the reports contained a clinical history (85.9%), information for certain prognostic indicators such as location and mass size was lacking. Grading with both Patnaik and Kiupel systems were described in 76.5% of reports with a single system being used in 7.1% and 15.2% of reports, respectively. Subcutaneous MCT were assigned a grading scheme in 67.2% of reports with 33.3% stating appropriate limitations. Surgical margins were reported in 92% of the reports with 77.2% describing deep and lateral margins separately. Tissue composing the deep margin was only described in 10.9% of the reports. The present results indicate reporting of MCT has variability across pathologists with inconsistencies present in the reporting of clinical history, margin evaluation and subcutaneous MCT grading. John Wiley and Sons Inc. 2018-06-07 /pmc/articles/PMC6090413/ /pubmed/29877634 http://dx.doi.org/10.1002/vms3.107 Text en © 2018 The Authors. Veterinary Medicine and Science Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Reagan, Jennifer K.
Selmic, Laura E.
Fallon, Caroline
Driskell, Elizabeth A.
Garrett, Laura D.
Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015
title Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015
title_full Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015
title_fullStr Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015
title_full_unstemmed Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015
title_short Evaluation of information presented within mast cell tumour histopathology reports in the United States: 2012–2015
title_sort evaluation of information presented within mast cell tumour histopathology reports in the united states: 2012–2015
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090413/
https://www.ncbi.nlm.nih.gov/pubmed/29877634
http://dx.doi.org/10.1002/vms3.107
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