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Research Article Open access CC BY 4.0

Primary Orbital Lymphoma – A Rare Challenging Diagnostic Entity

Nisha Marwah, Niti Dalal, Manali Satiza, Sunita Singh

Ophthalmology Research: An International Journal · pp. 18–21 · Published 2 Nov 2020

10.9734/or/2020/v13i430174

Abstract

The diagnosis of lymphoproliferative disorder of orbit is quite challenging as both Pseudolymphomas and Non‑Hodgkin’s lymphomas can occur in orbit. Primary orbital lymphoma is a rare entity comprising of 1-2% of Non‑Hodgkin’s lymphoma, majority of them are B‑cell type. It is a slow growing tumor. It presents in the age group of 50–70 years, with a slight female preponderance. Proptosis is the most common presentation. We, herein, report a case of 48 years old male presenting with right non-axial proptosis, watering of eye, blurring of vision and redness for the last 9 months. After thorough clinical and radiological evaluation, a biopsy was taken for histopathological examination. A primary diagnosis of Lymphoproliferative Disorder was made. Following this, a panel of immunohistochemical markers was applied and a final diagnosis of Non-Hodgkin Lymphoma, B-cell type was given.

Primary non hodgkin’s lymphoma B cell type orbit.

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