Plasma Cell Granulomas of the Central Nervous System

2006 ◽  
Vol 13 (1) ◽  
pp. 59-74
Author(s):  
Saleh Baeesa
2021 ◽  
Vol 21 ◽  
pp. S437-S438
Author(s):  
Carine Ribeiro Franzon ◽  
Andressa Oliveira Martin Wagner ◽  
Annelise Correa Wengerkievicz Lopes ◽  
Douglas Gebauer Bona ◽  
Talita Bertazzo Schmitz

2019 ◽  
Vol 59 (3) ◽  
pp. 135-139
Author(s):  
Takayuki Murase ◽  
Atsushi Inagaki ◽  
Ayako Masaki ◽  
Keiichiro Fujii ◽  
Tomoko Narita ◽  
...  

Neurosurgery ◽  
1994 ◽  
Vol 35 (4) ◽  
pp. 744-747 ◽  
Author(s):  
John Hsiang ◽  
David Moorhouse ◽  
David Barba

Neurosurgery ◽  
1994 ◽  
Vol 35 (4) ◽  
pp. 744???747 ◽  
Author(s):  
John Hsiang ◽  
David Moorhouse ◽  
David Barba

2021 ◽  
Vol 21 ◽  
pp. S257
Author(s):  
Carine Ribeiro Franzon ◽  
Andressa Oliveira Martin Wagner ◽  
Annelise Correa Wengerkievicz Lopes ◽  
Douglas Gebauer Bona ◽  
Talita Bertazzo Schmitz

Neurosurgery ◽  
1989 ◽  
Vol 24 (3) ◽  
pp. 429-434 ◽  
Author(s):  
Karen M. Weidenheim ◽  
Wallace G. Campbell ◽  
H. Warren Goldman

Abstract Hematopoietic proliferations rich in plasma cells rarely occur within the central nervous system without the involvement of other organ systems. Depending on their histological pattern and cellular composition, several different terms, including plasmacytoma, plasma cell granuloma, hyalinizing plasmacytic granulomatosis, and inflammatory meningioma, are used for these lesions. We report a left temporal dural lesion composed of plasma cells, lymphocytes, histiocytes, and rare eosinophils with hyaline changes and a suggestion of follicle formation, which stained predominantly for IgG and kappa light chains. This lesion arose in an otherwise healthy 52-year-old woman. Free kappa light chains without a monoclonal peak were found in the urine. We are aware of only two other heterogeneous, predominantly plasmacytic, solitary dural lesions that were found to be monoclonal on immunohistochemical examination. The label atypical monoclonal plasma cell hyperplasia appears to suit the morphological characteristics of our lesion. We suggest that a spectrum of solitary plasmacytic lesions may occur within the central nervous system and that atypical plasma cell hyperplasias have the potential to evolve into plasmacytoma. The preneoplastic nature of this lesion and its potential for evolution to malignant myeloma should be considered when planning treatment and lifelong follow-up for patients.


Neurosurgery ◽  
1989 ◽  
Vol 24 (3) ◽  
pp. 429???34 ◽  
Author(s):  
K M Weidenheim ◽  
W G Campbell ◽  
H W Goldman

2015 ◽  
Vol 2015 ◽  
pp. 1-5
Author(s):  
Christian W. Eskelund ◽  
Niels Frost Andersen

Primary plasma cell leukaemia (pPCL) is a rare and aggressive form of plasma cell malignancies with a very poor prognosis. Compared to other plasma cell malignancies the tendency to extramedullary spread is increased; however central nervous system (CNS) involvement is rare and only reported in few cases. We report the case of a 61-year-old man who was diagnosed with pPCL and achieved a complete remission after autologous stem cell transplantation but had a relapse in the CNS without systemic disease.


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