Primary central nervous system and retinal lymphoma

Manmeet S. Ahluwalia, Saurabh Dahiya, Mary E. Aronow, David Peereboom, Arun D. Singh

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Primary lymphoma of the central nervous system (CNS) is considered a variant of extra-nodal non-Hodgkin’s lymphoma (NHL), a high-grade B-cell malignancy associated with a median survival ranging from one to 8 years depending on factors such as age and Karnofsky performance status [1]. Primary CNS lymphoma (PCNSL) originates in the brain parenchyma, spinal cord, leptomeninges, and eyes [2]. Formerly used descriptors such as “reticulum cell sarcoma” and “microgliomatosis” are no longer preferred as both misleadingly imply that the lymphoma arises from transformed reticulum or microglial cells. Primary intraocular lymphoma (PCNSL-O) is a variant of PCNSL with predominantly ophthalmic involvement. As vitreoretinal manifestations are the dominant feature, the term primary vitreoretinal lymphoma (PVRL) is commonly used. In contrast, other forms of ocular lymphoma typically affect the adnexal structures or uveal tract. The distinction is important as uveal and ocular adnexal lymphoma are usually low-grade, indolent, B-cell lymphomas that behave similarly to extra-nodal marginal zone lymphoma(EMZL) found elsewhere in the body [3].

Original languageEnglish (US)
Title of host publicationClinical Ophthalmic Oncology: Retinal Tumors
PublisherSpringer Berlin Heidelberg
Pages75-90
Number of pages16
ISBN (Print)9783642394898, 9783642394881
DOIs
StatePublished - Jan 1 2014
Externally publishedYes

ASJC Scopus subject areas

  • Medicine(all)

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