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Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review

Cerebral amyloidomas are rare cerebral mass lesions often associated with significant morbidity. Cerebral amyloid accumulation can be the result of a number of disease states and it is crucial for proper patient care to identify the pathogenic process leading to amyloidoma formation. Low grade clona...

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Detalles Bibliográficos
Autores principales: Jagannathan, Geetha, Uppal, Guldeep, Judy, Kevin, Curtis, Mark T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038588/
https://www.ncbi.nlm.nih.gov/pubmed/30046502
http://dx.doi.org/10.1155/2018/5083234
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author Jagannathan, Geetha
Uppal, Guldeep
Judy, Kevin
Curtis, Mark T.
author_facet Jagannathan, Geetha
Uppal, Guldeep
Judy, Kevin
Curtis, Mark T.
author_sort Jagannathan, Geetha
collection PubMed
description Cerebral amyloidomas are rare cerebral mass lesions often associated with significant morbidity. Cerebral amyloid accumulation can be the result of a number of disease states and it is crucial for proper patient care to identify the pathogenic process leading to amyloidoma formation. Low grade clonal B-cell processes are one cause of cerebral amyloidomas. We report a case of an 87-year-old woman who presented with a lymphoplasmacytic lymphoma associated cerebral amyloidoma complicated by cerebral hemorrhage, discuss the proper workup of this disease entity, and present a review of the literature on this topic.
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spelling pubmed-60385882018-07-25 Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review Jagannathan, Geetha Uppal, Guldeep Judy, Kevin Curtis, Mark T. Case Rep Pathol Case Report Cerebral amyloidomas are rare cerebral mass lesions often associated with significant morbidity. Cerebral amyloid accumulation can be the result of a number of disease states and it is crucial for proper patient care to identify the pathogenic process leading to amyloidoma formation. Low grade clonal B-cell processes are one cause of cerebral amyloidomas. We report a case of an 87-year-old woman who presented with a lymphoplasmacytic lymphoma associated cerebral amyloidoma complicated by cerebral hemorrhage, discuss the proper workup of this disease entity, and present a review of the literature on this topic. Hindawi 2018-06-26 /pmc/articles/PMC6038588/ /pubmed/30046502 http://dx.doi.org/10.1155/2018/5083234 Text en Copyright © 2018 Geetha Jagannathan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jagannathan, Geetha
Uppal, Guldeep
Judy, Kevin
Curtis, Mark T.
Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review
title Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review
title_full Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review
title_fullStr Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review
title_full_unstemmed Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review
title_short Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review
title_sort cerebral amyloidoma resulting from central nervous system lymphoplasmacytic lymphoma: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038588/
https://www.ncbi.nlm.nih.gov/pubmed/30046502
http://dx.doi.org/10.1155/2018/5083234
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AT judykevin cerebralamyloidomaresultingfromcentralnervoussystemlymphoplasmacyticlymphomaacasereportandliteraturereview
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