Lymphomatosis Cerebri: A diagnostic dilemma

Author:

Khan Sibgha1ORCID,Mubarak Fatima1,Minhas Khurram1ORCID,Kanwar Dureshahwar1,Chen Robert Chun2

Affiliation:

1. Department of Radiology, Aga Khan University Hospital, National Stadium Road, Karachi, Pakistan

2. Department of Neuroradiology, Singapore General hospital, Singapore

Abstract

Background Lymphomatosis cerebri (LC) is a rare manifestation of primary central nervous system lymphoma (PCNSL) with only a few cases reported in the literature, appearing as diffuse infiltrating process rather than a solitary mass. It is a non-Hodgkin’s type of lymphoma and is usually of the B-cell type origin. Purpose We intend to report this unique case of LC which came across as a diagnostic challenge. Methods A 53-year-old gentleman presented with complaints of two episodes of seizures 24 h apart followed by postictal confusion for 10–15 min. He underwent multiple MRI scans and underwent a biopsy of the lesion which reported infection, but he did not benefit from the treatment. Result The imaging was reviewed, suspicion of LC was raised and a review of histopathology was requested which later confirmed primary CNS lymphoma. Conclusion LC is a rare but established manifestation of PCNSL which mimics multiple other conditions. Understanding of the imaging pattern is important in making the diagnosis and differentiating it from other mimic conditions.

Publisher

SAGE Publications

Subject

General Neuroscience

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