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Current Molecular Medicine

Editor-in-Chief

ISSN (Print): 1566-5240
ISSN (Online): 1875-5666

Molecular Analysis of Primary Central Nervous System and Primary Intraocular Lymphomas.

Author(s): N. Tuaillon and C. C. Chan

Volume 1, Issue 2, 2001

Page: [259 - 272] Pages: 14

DOI: 10.2174/1566524013363915

Price: $65

Abstract

Primary central nervous system lymphoma (PCNSL) is usually a large B-cell, high grade non-Hodgkins lymphoma (NHL) classified as a diffuse large cell lymphoma (DLCL). In rare cases, however, T cell lymphomas have been described. Although a relatively rare tumor, the incidence of PCNSL has increased dramatically over the past 15 years in both immuno-competent and immuno-compromised patients. The disease is aggressive with a 5-year survival rate of less than 25 percent. The cause of death is progressive and recurrent disease in the CNS, despite aggressive treatment. Approximately 20-25percent of patients with PCNSL also have primary intra-ocular lymphoma (PIOL). PCNSL and PIOL are closely related and inter-connected pathologies involving two immune privileged sites. The study of PCNSL and PIOL has been limited due to the fact that viable malignant cells are rare and difficult to recognize. Moreover, the cells are difficult to culture and to date there is no good animal model for the disease. Here, we will present the current literature on the disease. In particular, we will present data suggesting that PCNSL in immuno-compromised and AIDS patients may correspond to two different pathologies. Furthermore, we will discuss how the study of these lymphomas can benefit from new advanced molecular biology techniques including single cell PCR and laser capture microdissection (LCM). PCNSL and PIOL are aggressive tumors, therefore, early diagnosis and prompt, aggressive treatment may improve prognosis. Advanced molecular biology will help delineate the oncogenesis of PCNSL and PIOL.

Keywords: Central Nervous System, Intraocular Lymphomas, CENTRAL NERVOUS SYSTEM LYMPHOMA, MALIGNANT B CELLS, TUMOR CELLS, ANTIGENIC SELECTION, INFECTIOUS AGENTS, APOPTOSIS


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