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Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review

Mucous membrane plasmacytosis (MMP) is an uncommon variant of mucositis represented by a polyclonal plasma cell infiltration of mucosal tissue. Various clinical presentations in the upper airway have been reported ranging from erythematous mucosa to fungating masses. Histologic features include muco...

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Detalles Bibliográficos
Autores principales: Makarenko, Vladislav V., Vaezi, Alec E., Brettler, Doreen B., Hutchinson, Lloyd, Woda, Bruce A., Chen, Benjamin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906643/
https://www.ncbi.nlm.nih.gov/pubmed/31867207
http://dx.doi.org/10.1016/j.lrr.2019.100190
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author Makarenko, Vladislav V.
Vaezi, Alec E.
Brettler, Doreen B.
Hutchinson, Lloyd
Woda, Bruce A.
Chen, Benjamin J.
author_facet Makarenko, Vladislav V.
Vaezi, Alec E.
Brettler, Doreen B.
Hutchinson, Lloyd
Woda, Bruce A.
Chen, Benjamin J.
author_sort Makarenko, Vladislav V.
collection PubMed
description Mucous membrane plasmacytosis (MMP) is an uncommon variant of mucositis represented by a polyclonal plasma cell infiltration of mucosal tissue. Various clinical presentations in the upper airway have been reported ranging from erythematous mucosa to fungating masses. Histologic features include mucosal epithelial hyperplasia or psoriasiform changes with a dense submucosal infiltrate of polytypic plasma cells. Molecular studies for immunoglobulin gene rearrangement should be performed in all cases of MMP to rule out clonal neoplastic expansion of plasma cells. We present a case of MMP with over 15 years of clinical follow-up, emphasizing the relatively benign clinical course of this disorder.
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spelling pubmed-69066432019-12-20 Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review Makarenko, Vladislav V. Vaezi, Alec E. Brettler, Doreen B. Hutchinson, Lloyd Woda, Bruce A. Chen, Benjamin J. Leuk Res Rep Article Mucous membrane plasmacytosis (MMP) is an uncommon variant of mucositis represented by a polyclonal plasma cell infiltration of mucosal tissue. Various clinical presentations in the upper airway have been reported ranging from erythematous mucosa to fungating masses. Histologic features include mucosal epithelial hyperplasia or psoriasiform changes with a dense submucosal infiltrate of polytypic plasma cells. Molecular studies for immunoglobulin gene rearrangement should be performed in all cases of MMP to rule out clonal neoplastic expansion of plasma cells. We present a case of MMP with over 15 years of clinical follow-up, emphasizing the relatively benign clinical course of this disorder. Elsevier 2019-11-27 /pmc/articles/PMC6906643/ /pubmed/31867207 http://dx.doi.org/10.1016/j.lrr.2019.100190 Text en © 2019 The Author(s) http://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 Article
Makarenko, Vladislav V.
Vaezi, Alec E.
Brettler, Doreen B.
Hutchinson, Lloyd
Woda, Bruce A.
Chen, Benjamin J.
Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review
title Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review
title_full Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review
title_fullStr Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review
title_full_unstemmed Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review
title_short Laryngeal mucous membrane plasmacytosis with 15 year follow-up: Case report and literature review
title_sort laryngeal mucous membrane plasmacytosis with 15 year follow-up: case report and literature review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906643/
https://www.ncbi.nlm.nih.gov/pubmed/31867207
http://dx.doi.org/10.1016/j.lrr.2019.100190
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