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P. H. Tu, C. Giannini, A. R. Judkins, J. M. Schwalb, R. Burack, B. P. O’Neill, A. T. Yachnis, P. C. Burger, B. W. Scheithauer and A. Perry, “Clinicopathologic and Genetic Profile of Intracranial Marginal Zone Lymphoma: A Primary Low-Grade CNS Lymphoma That Mimics Meningioma,” Journal of Clinical Oncology, Vol. 23, No. 24, 2005, pp. 5718-5727. doi:10.1200/JCO.2005.17.624

has been cited by the following article:

• TITLE: Primary CNS Marginal Zone Lymphoma: A Case Report and Review of the Literature

  AUTHORS: Barina Aqil, Emilie Rouah, Gordana Verstovsek

  KEYWORDS: Primary CNS Lymphoma; MZL

  JOURNAL NAME: Open Journal of Pathology, Vol.3 No.2, April 19, 2013

  ABSTRACT: Primary central nervous system lymphoma (PCNSL) is a rare subtype of extranodal non-Hodgkin lymphoma (NHL) located in the craniospinal axis (affecting CNS, meninges and eye) without evidence of a systemic primary tumor. CNS lymphomas are typically high grade, large cell lymphomas; low grade CNS lymphomas are rare. We encountered a case of 48-year old patient with recurrent episodes of seizures, weakness of bilateral extremities and memory loss. On MRI and CT scan, a 2.0 cm area of ill-defined enhancement with associated edema was present in the left frontal subcortex. The biopsy revealed an infiltrate of small lymphocytes expressing pan B-cell markers and an immunoprofile consistent with an extranodal marginal zone B cell lymphomas of mucosa associated lymphoid tissue (MALT). Clonal rearrangement was demonstrated by PCR analysis. Subsequently, the patient was treated with radiation therapy and responded well, with decrease in the size of the lesion. He is alive and well for 1 year and 3 months up to the date of this report.