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Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’

Introduction: pMCT is defined as a variant of papillary carcinoma that measures≤1 cm in diameter and which is characterized by an excellent prognosis. Recently, a proposal has been advanced to use the designation of papillary mirotumour (pMT) for pMCTs with no risk factors . In this study, we aimed...

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Autores principales: Ben Rejeb, Sarra, Rejeb, Dorra, Aloui, Marwa, Chouchen, Hamdi, Turki, Senda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tunisian Society of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703906/
https://www.ncbi.nlm.nih.gov/pubmed/36571744
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author Ben Rejeb, Sarra
Rejeb, Dorra
Aloui, Marwa
Chouchen, Hamdi
Turki, Senda
author_facet Ben Rejeb, Sarra
Rejeb, Dorra
Aloui, Marwa
Chouchen, Hamdi
Turki, Senda
author_sort Ben Rejeb, Sarra
collection PubMed
description Introduction: pMCT is defined as a variant of papillary carcinoma that measures≤1 cm in diameter and which is characterized by an excellent prognosis. Recently, a proposal has been advanced to use the designation of papillary mirotumour (pMT) for pMCTs with no risk factors . In this study, we aimed to reclassify pMCTs according to the Porto proposal(Pp) criteria. Methods: We have retrospectively collected cases of pMCT diagnosed in our pathology department over a period of 10years(2012-2022). Clinical and pathological parameters have been retrieved from the patient’s medical records and pathological reports.We have evaluated all cases following the criteria of Pp.Cases that fulfilled all the criteria have been reclassified as Pmt.We have briefly compared the clinical outcomes in both groups. Results: 29 cases of pMCT was found.Mean age of patients was 46,6years-old(17-67) with a female predominance (sex ratio=0,45).23cases of pMCT were incidentally discovered.The tumor was located in the right thyroid lobe in 15cases.The mean size of the tumor was 5,2mm.Multifocality was observed in 5cases.A total of 17 cases could be classified as pMT according to the Pp.Only one patient developed pulmonary metastasis and local recurrence;however it was related to the papillary carcinoma firstly diagnosed in his contralateral lobe.Clinical outcome was also good in the group of papillary microcarcinoma (pMC) with no recurrence or distant metastasis. Conclusion: According to the Pp,>50% of pMCT could be reclassified as pMT which could reduce the psychological impact and overtreatment.Further studies with large sample size and molecular analysis are however needed in order to definitively validate and generalize the use of Porto proposal.
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spelling pubmed-97039062022-12-07 Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’ Ben Rejeb, Sarra Rejeb, Dorra Aloui, Marwa Chouchen, Hamdi Turki, Senda Tunis Med Article Introduction: pMCT is defined as a variant of papillary carcinoma that measures≤1 cm in diameter and which is characterized by an excellent prognosis. Recently, a proposal has been advanced to use the designation of papillary mirotumour (pMT) for pMCTs with no risk factors . In this study, we aimed to reclassify pMCTs according to the Porto proposal(Pp) criteria. Methods: We have retrospectively collected cases of pMCT diagnosed in our pathology department over a period of 10years(2012-2022). Clinical and pathological parameters have been retrieved from the patient’s medical records and pathological reports.We have evaluated all cases following the criteria of Pp.Cases that fulfilled all the criteria have been reclassified as Pmt.We have briefly compared the clinical outcomes in both groups. Results: 29 cases of pMCT was found.Mean age of patients was 46,6years-old(17-67) with a female predominance (sex ratio=0,45).23cases of pMCT were incidentally discovered.The tumor was located in the right thyroid lobe in 15cases.The mean size of the tumor was 5,2mm.Multifocality was observed in 5cases.A total of 17 cases could be classified as pMT according to the Pp.Only one patient developed pulmonary metastasis and local recurrence;however it was related to the papillary carcinoma firstly diagnosed in his contralateral lobe.Clinical outcome was also good in the group of papillary microcarcinoma (pMC) with no recurrence or distant metastasis. Conclusion: According to the Pp,>50% of pMCT could be reclassified as pMT which could reduce the psychological impact and overtreatment.Further studies with large sample size and molecular analysis are however needed in order to definitively validate and generalize the use of Porto proposal. Tunisian Society of Medical Sciences 2022-07 2022-07-01 /pmc/articles/PMC9703906/ /pubmed/36571744 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 Unported License. To view a copy of this license, visit https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Ben Rejeb, Sarra
Rejeb, Dorra
Aloui, Marwa
Chouchen, Hamdi
Turki, Senda
Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’
title Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’
title_full Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’
title_fullStr Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’
title_full_unstemmed Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’
title_short Reclassification du microcarcinome papillaire de la thyroîde (pMCT) selon les critères de ‘’ la proposition de Porto’’
title_sort reclassification du microcarcinome papillaire de la thyroîde (pmct) selon les critères de ‘’ la proposition de porto’’
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703906/
https://www.ncbi.nlm.nih.gov/pubmed/36571744
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