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Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma

Pure red cell aplasia is an uncommon paraneoplastic syndrome of thymoma. Myasthenia gravis is the most common paraneoplastic syndrome associated with thymoma. We present a case of a 79-year-old Pacific Islander female who presented with profound fatigue, generalized weakness, significant unintention...

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Autores principales: Lee, Sun Yong, Gill, Amandeep, Jung, Syung Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431916/
https://www.ncbi.nlm.nih.gov/pubmed/32864051
http://dx.doi.org/10.1080/20009666.2020.1770019
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author Lee, Sun Yong
Gill, Amandeep
Jung, Syung Min
author_facet Lee, Sun Yong
Gill, Amandeep
Jung, Syung Min
author_sort Lee, Sun Yong
collection PubMed
description Pure red cell aplasia is an uncommon paraneoplastic syndrome of thymoma. Myasthenia gravis is the most common paraneoplastic syndrome associated with thymoma. We present a case of a 79-year-old Pacific Islander female who presented with profound fatigue, generalized weakness, significant unintentional weight loss, bilateral ptosis, and anemia. The bone marrow biopsy showed near absence of erythroid elements consistent with pure red cell aplasia. Ice-pack test was consistent with myasthenia gravis and computed tomography of the chest demonstrated a thymoma. The patient was started on immunosuppressive treatment with prednisone and cyclosporine. This case demonstrates a rare combination of paraneoplastic manifestations of thymoma: pure red cell aplasia and myasthenia gravis.
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spelling pubmed-74319162020-08-27 Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma Lee, Sun Yong Gill, Amandeep Jung, Syung Min J Community Hosp Intern Med Perspect Case Report Pure red cell aplasia is an uncommon paraneoplastic syndrome of thymoma. Myasthenia gravis is the most common paraneoplastic syndrome associated with thymoma. We present a case of a 79-year-old Pacific Islander female who presented with profound fatigue, generalized weakness, significant unintentional weight loss, bilateral ptosis, and anemia. The bone marrow biopsy showed near absence of erythroid elements consistent with pure red cell aplasia. Ice-pack test was consistent with myasthenia gravis and computed tomography of the chest demonstrated a thymoma. The patient was started on immunosuppressive treatment with prednisone and cyclosporine. This case demonstrates a rare combination of paraneoplastic manifestations of thymoma: pure red cell aplasia and myasthenia gravis. Taylor & Francis 2020-06-14 /pmc/articles/PMC7431916/ /pubmed/32864051 http://dx.doi.org/10.1080/20009666.2020.1770019 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lee, Sun Yong
Gill, Amandeep
Jung, Syung Min
Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
title Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
title_full Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
title_fullStr Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
title_full_unstemmed Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
title_short Pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
title_sort pure red cell aplasia and seronegative myasthenia gravis in association with thymoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7431916/
https://www.ncbi.nlm.nih.gov/pubmed/32864051
http://dx.doi.org/10.1080/20009666.2020.1770019
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