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

المؤلفون المشاركون

Curtis, Mark
Jagannathan, Geetha
Uppal, Guldeep
Judy, Kevin

المصدر

Case Reports in Pathology

العدد

المجلد 2018، العدد 2018 (31 ديسمبر/كانون الأول 2018)، ص ص. 1-6، 6ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2018-06-26

دولة النشر

مصر

عدد الصفحات

6

التخصصات الرئيسية

الأمراض

الملخص EN

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.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Jagannathan, Geetha& Uppal, Guldeep& Judy, Kevin& Curtis, Mark. 2018. Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review. Case Reports in Pathology،Vol. 2018, no. 2018, pp.1-6.
https://search.emarefa.net/detail/BIM-1148764

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Jagannathan, Geetha…[et al.]. Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review. Case Reports in Pathology No. 2018 (2018), pp.1-6.
https://search.emarefa.net/detail/BIM-1148764

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Jagannathan, Geetha& Uppal, Guldeep& Judy, Kevin& Curtis, Mark. Cerebral Amyloidoma Resulting from Central Nervous System Lymphoplasmacytic Lymphoma: A Case Report and Literature Review. Case Reports in Pathology. 2018. Vol. 2018, no. 2018, pp.1-6.
https://search.emarefa.net/detail/BIM-1148764

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1148764