Literature DB >> 18499338

Primary leptomeningeal B-cell lymphoma of MALT-type in statu nascendi: a case report and review of the literature.

Serge Weis1, Ida C Llenos.   

Abstract

A 29-year-old Caucasian female suffering from bipolar disorder, mixed, moderate with psychotic features (DSM-IV 296.64) and panic disorder without agoraphobia (DSM-IV 300.01) died as a result of an accidental overdose. Upon histopathological examination of the brain, as an incidental finding, a small lesion (1mm x 2mm) composed of heterogeneous small lymphocytic cells (CD20-positive) including centrocyte-like cells, a few small lymphocytes and rare immunoblast-like cells was evident. The diagnosis of primary leptomeningeal MALT-type lymphoma was made. Due to its small size and lack of space-occupying characteristics, the lesion is considered to be in statu nascendi. This case adds another aspect to the rare entity of primary leptomeningeal lymphomas.

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Year:  2008        PMID: 18499338     DOI: 10.1016/j.clineuro.2008.04.005

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  2 in total

1.  Primary leptomeningeal lymphoma: International Primary CNS Lymphoma Collaborative Group report.

Authors:  Jennie W Taylor; Eoin P Flanagan; Brian P O'Neill; Tali Siegal; Antonio Omuro; Lisa Deangelis; Joachim Baehring; Ryo Nishikawa; Fernando Pinto; Marc Chamberlain; Khe Hoang-Xuan; Alberto Gonzalez-Aguilar; Tracy Batchelor; Jean-Yves Blay; Agnieszka Korfel; Rebecca A Betensky; Maria-Beatriz S Lopes; David Schiff
Journal:  Neurology       Date:  2013-10-09       Impact factor: 9.910

Review 2.  Rare central nervous system lymphomas.

Authors:  Furqaan Ahmed Kaji; Nicolás Martinez-Calle; Vishakha Sovani; Christopher Paul Fox
Journal:  Br J Haematol       Date:  2022-03-16       Impact factor: 8.615

  2 in total

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