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Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome

Immunohistochemistry for mismatch repair proteins and microsatellite instability testing are recommended screening methods for Lynch syndrome. They have a good sensitivity and specificity, allowing for directed genetic testing and diagnosis. We report a case of Lynch syndrome with retained MMR prote...

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Autores principales: Nagabhushana, Prerana, Kumari, Snigdha, Rohilla, Minakshi, Srinivasan, Radhika, Arora, Aashima, Rastogi, Pulkit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416636/
https://www.ncbi.nlm.nih.gov/pubmed/34504932
http://dx.doi.org/10.1016/j.gore.2021.100854
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author Nagabhushana, Prerana
Kumari, Snigdha
Rohilla, Minakshi
Srinivasan, Radhika
Arora, Aashima
Rastogi, Pulkit
author_facet Nagabhushana, Prerana
Kumari, Snigdha
Rohilla, Minakshi
Srinivasan, Radhika
Arora, Aashima
Rastogi, Pulkit
author_sort Nagabhushana, Prerana
collection PubMed
description Immunohistochemistry for mismatch repair proteins and microsatellite instability testing are recommended screening methods for Lynch syndrome. They have a good sensitivity and specificity, allowing for directed genetic testing and diagnosis. We report a case of Lynch syndrome with retained MMR protein expression who later showed an MLH1 gene variant on genetic testing (Next Generation Sequencing) requested because of the clinical presentation of metachronous colonic and endometrial carcinoma. This report makes the case for strong clinical suspicion and directed genetic testing despite initial screen negative results.
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spelling pubmed-84166362021-09-08 Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome Nagabhushana, Prerana Kumari, Snigdha Rohilla, Minakshi Srinivasan, Radhika Arora, Aashima Rastogi, Pulkit Gynecol Oncol Rep Case Reports and Case Series Immunohistochemistry for mismatch repair proteins and microsatellite instability testing are recommended screening methods for Lynch syndrome. They have a good sensitivity and specificity, allowing for directed genetic testing and diagnosis. We report a case of Lynch syndrome with retained MMR protein expression who later showed an MLH1 gene variant on genetic testing (Next Generation Sequencing) requested because of the clinical presentation of metachronous colonic and endometrial carcinoma. This report makes the case for strong clinical suspicion and directed genetic testing despite initial screen negative results. Elsevier 2021-08-28 /pmc/articles/PMC8416636/ /pubmed/34504932 http://dx.doi.org/10.1016/j.gore.2021.100854 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Reports and Case Series
Nagabhushana, Prerana
Kumari, Snigdha
Rohilla, Minakshi
Srinivasan, Radhika
Arora, Aashima
Rastogi, Pulkit
Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome
title Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome
title_full Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome
title_fullStr Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome
title_full_unstemmed Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome
title_short Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome
title_sort discordant immunohistochemistry in an unusual mlh1 gene variant in a case of lynch syndrome
topic Case Reports and Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416636/
https://www.ncbi.nlm.nih.gov/pubmed/34504932
http://dx.doi.org/10.1016/j.gore.2021.100854
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