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An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)

POEMS syndrome is an acronym for polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes, which is a rare paraneoplastic disease of monoclonal plasma cells. A mandatory criterion to diagnose POEMS syndrome is the presence of a monoclonal plasma cell dyscrasia in which pl...

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Detalles Bibliográficos
Autores principales: Afridi, Faraz, Otoya, Jorge, Bunting, Samantha F, Chaaya, Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384847/
https://www.ncbi.nlm.nih.gov/pubmed/28405536
http://dx.doi.org/10.7759/cureus.1086
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author Afridi, Faraz
Otoya, Jorge
Bunting, Samantha F
Chaaya, Gerard
author_facet Afridi, Faraz
Otoya, Jorge
Bunting, Samantha F
Chaaya, Gerard
author_sort Afridi, Faraz
collection PubMed
description POEMS syndrome is an acronym for polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes, which is a rare paraneoplastic disease of monoclonal plasma cells. A mandatory criterion to diagnose POEMS syndrome is the presence of a monoclonal plasma cell dyscrasia in which plasma cell leukemia is the most aggressive form. Early identification of the features of the POEMS syndrome is critical for patients to identify an underlying plasma cell dyscrasias and to reduce the morbidity and mortality of the disease by providing early therapy. We present a case of a 64-year-old male who presented with non-specific symptoms and was found to have primary plasma cell leukemia, which was part of his unfortunate POEMS syndrome.
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spelling pubmed-53848472017-04-12 An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS) Afridi, Faraz Otoya, Jorge Bunting, Samantha F Chaaya, Gerard Cureus Oncology POEMS syndrome is an acronym for polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes, which is a rare paraneoplastic disease of monoclonal plasma cells. A mandatory criterion to diagnose POEMS syndrome is the presence of a monoclonal plasma cell dyscrasia in which plasma cell leukemia is the most aggressive form. Early identification of the features of the POEMS syndrome is critical for patients to identify an underlying plasma cell dyscrasias and to reduce the morbidity and mortality of the disease by providing early therapy. We present a case of a 64-year-old male who presented with non-specific symptoms and was found to have primary plasma cell leukemia, which was part of his unfortunate POEMS syndrome. Cureus 2017-03-08 /pmc/articles/PMC5384847/ /pubmed/28405536 http://dx.doi.org/10.7759/cureus.1086 Text en Copyright © 2017, Afridi et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Oncology
Afridi, Faraz
Otoya, Jorge
Bunting, Samantha F
Chaaya, Gerard
An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)
title An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)
title_full An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)
title_fullStr An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)
title_full_unstemmed An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)
title_short An Unfortunate Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Change (POEMS)
title_sort unfortunate polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin change (poems)
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384847/
https://www.ncbi.nlm.nih.gov/pubmed/28405536
http://dx.doi.org/10.7759/cureus.1086
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