Primary T-Cell–Rich B-Cell Lymphoma Masquerading as a Meningioma

Author:

Amaker Barbara H.12,Ghatak Nitya R.2,Jebraili Sean A.2,Ferreira-Gonzalez Andrea2,Kornstein Michael J.2

Affiliation:

1. Reprints: Barbara H. Amaker, MD, Department of Pathology, Division of Neuropathology, Medical College of Virginia/Virginia Commonwealth University, PO Box 980017, Richmond, VA 23298-0017.

2. From the Department of Pathology (Drs Amaker, Ghatak, Ferreira-Gonzalez, and Kornstein) and Department of Surgery, Division of Neurosurgery (Dr Jebraili), Medical College of Virginia, Virginia Commonwealth University, Richmond, Va.

Abstract

Abstract Primary dural lymphoma is rare, and few of the small number of cases reported to date have been classified using immunohistochemical techniques. To our knowledge, we report the first case of T-cell–rich B-cell lymphoma (diffuse mixed small cell and large cell) presenting as a solitary intracranial dural mass. Cytologic and frozen sections prepared during intraoperative consultation revealed a polymorphic population of lymphocytes suspicious for an inflammatory process. Permanent sections of the dura showed a diffusely infiltrating mass composed of mature lymphocytes peppered with large atypical lymphocytes. Immunohistochemical stains identified the small lymphocytes as T cells (CD3 and CD43) and the large atypical lymphocytes as B cells (CD20). Evidence of rearranged immunoglobulin heavy-chain genes demonstrated B-cell monoclonality. Differentiating between inflammatory and neoplastic lymphocytic masses of the dura obviously has important therapeutic and prognostic significance and may require immunohistochemical and molecular techniques.

Publisher

Archives of Pathology and Laboratory Medicine

Subject

Medical Laboratory Technology,General Medicine,Pathology and Forensic Medicine

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