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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Format: | Article |
Language: | English |
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Wiley
2018-01-01
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Series: | Case Reports in Pathology |
Online Access: | http://dx.doi.org/10.1155/2018/5083234 |
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author | Geetha Jagannathan Guldeep Uppal Kevin Judy Mark T. Curtis |
author_facet | Geetha Jagannathan Guldeep Uppal Kevin Judy Mark T. Curtis |
author_sort | Geetha Jagannathan |
collection | DOAJ |
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. |
format | Article |
id | doaj-art-5744839b33214b1ead31f2dea7e734f7 |
institution | Kabale University |
issn | 2090-6781 2090-679X |
language | English |
publishDate | 2018-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Pathology |
spelling | doaj-art-5744839b33214b1ead31f2dea7e734f72025-02-03T01:02:52ZengWileyCase Reports in Pathology2090-67812090-679X2018-01-01201810.1155/2018/50832345083234Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature ReviewGeetha Jagannathan0Guldeep Uppal1Kevin Judy2Mark T. Curtis3Department of Pathology, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USADepartment of Pathology, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USADepartment of Neurosurgery, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USADepartment of Pathology, Thomas Jefferson University Hospital, Philadelphia, PA 19107, USACerebral 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.http://dx.doi.org/10.1155/2018/5083234 |
spellingShingle | Geetha Jagannathan Guldeep Uppal Kevin Judy Mark T. Curtis Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review Case Reports in Pathology |
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 |
url | http://dx.doi.org/10.1155/2018/5083234 |
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