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A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels

Isolated myeloid sarcoma is an uncommon subtype of acute myeloid leukemia associated with variable prognosis. We present the case of a previously healthy 30-year-old man presenting with chest pain and weight loss who was found to have a large mediastinal mass. Biopsy of the mass was consistent with...

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Autores principales: Walker, Margaret, Folstad, Matthew, Smith-Simmer, Kelcy, Reinig, Erica, Nadiminti, Kalyan, Lovrien, Lauren, Churpek, Jane E., Banaszak, Lauren G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076140/
https://www.ncbi.nlm.nih.gov/pubmed/35573754
http://dx.doi.org/10.14740/jh983
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author Walker, Margaret
Folstad, Matthew
Smith-Simmer, Kelcy
Reinig, Erica
Nadiminti, Kalyan
Lovrien, Lauren
Churpek, Jane E.
Banaszak, Lauren G.
author_facet Walker, Margaret
Folstad, Matthew
Smith-Simmer, Kelcy
Reinig, Erica
Nadiminti, Kalyan
Lovrien, Lauren
Churpek, Jane E.
Banaszak, Lauren G.
author_sort Walker, Margaret
collection PubMed
description Isolated myeloid sarcoma is an uncommon subtype of acute myeloid leukemia associated with variable prognosis. We present the case of a previously healthy 30-year-old man presenting with chest pain and weight loss who was found to have a large mediastinal mass. Biopsy of the mass was consistent with isolated myeloid sarcoma. A somatic tumor sequencing panel revealed an EGFR T790M variant, which was later confirmed to be of germline origin. Germline EGFR T790M variants are associated with a hereditary predisposition to lung cancer, though myeloid malignancies have not yet been described. To our knowledge, this is the first reported case of myeloid sarcoma in a patient with an underlying germline EGFR T790M mutation. As somatic tumor sequencing panels become more commonplace, it is important to recognize potential germline variants in order to facilitate appropriate referral for genetic counseling, perform confirmatory genetic testing, and to develop a personalized treatment and surveillance plan for patients and their families.
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spelling pubmed-90761402022-05-12 A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels Walker, Margaret Folstad, Matthew Smith-Simmer, Kelcy Reinig, Erica Nadiminti, Kalyan Lovrien, Lauren Churpek, Jane E. Banaszak, Lauren G. J Hematol Case Report Isolated myeloid sarcoma is an uncommon subtype of acute myeloid leukemia associated with variable prognosis. We present the case of a previously healthy 30-year-old man presenting with chest pain and weight loss who was found to have a large mediastinal mass. Biopsy of the mass was consistent with isolated myeloid sarcoma. A somatic tumor sequencing panel revealed an EGFR T790M variant, which was later confirmed to be of germline origin. Germline EGFR T790M variants are associated with a hereditary predisposition to lung cancer, though myeloid malignancies have not yet been described. To our knowledge, this is the first reported case of myeloid sarcoma in a patient with an underlying germline EGFR T790M mutation. As somatic tumor sequencing panels become more commonplace, it is important to recognize potential germline variants in order to facilitate appropriate referral for genetic counseling, perform confirmatory genetic testing, and to develop a personalized treatment and surveillance plan for patients and their families. Elmer Press 2022-04 2022-04-12 /pmc/articles/PMC9076140/ /pubmed/35573754 http://dx.doi.org/10.14740/jh983 Text en Copyright 2022, Walker et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Walker, Margaret
Folstad, Matthew
Smith-Simmer, Kelcy
Reinig, Erica
Nadiminti, Kalyan
Lovrien, Lauren
Churpek, Jane E.
Banaszak, Lauren G.
A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
title A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
title_full A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
title_fullStr A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
title_full_unstemmed A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
title_short A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
title_sort case of isolated myeloid sarcoma associated with germline egfr t790m variant: the importance of recognizing potential germline variants on somatic tumor sequencing panels
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076140/
https://www.ncbi.nlm.nih.gov/pubmed/35573754
http://dx.doi.org/10.14740/jh983
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