Abstract

IntroductionOcular lymphomas account for five to 10 percent of all extra-nodal lymphomas. Primary uveal lymphoma is quite a rare entity and usually unilateral. We present a case of a primary uveal lymphoma with conjunctival and orbital extension, successfully managed with oral chlorambucil.Case presentationA 71-year-old Caucasian man presented to our facility with visual loss in his only functioning eye (left). On clinical examination, we found a conjunctival lesion with a choroidal infiltration and a secondary retinal detachment. Ultrasound and magnetic resonance imaging studies revealed a choroidal tumour mass and two other lesions around the optic nerve. Results from an incisional biopsy revealed a low-grade B-cell lymphoma (CD20+, CD43+, bcl2+, CD3-). A diagnosis of primary uveal lymphoma was made. Our patient was started on a chemotherapy regime with no effect, and then oral chlorambucil was administered, with a relatively good result. At 10 months after the start of chlorambucil treatment, a best-corrected visual acuity of 0.4 was recorded, the choroidal mass had practically disappeared and the extra-ocular lesions had shrunk.ConclusionsIn all, 61 to 80 cases of primary uveal lymphoma have already been described in the literature. Generally, it is an indolent tumor with a good prognosis. However, there are some reports of aggressive tumor behavior a few years after initial diagnosis (about eight percent of cases). Other treatment options are orbital irradiation at low doses (20 to 40 Gy) or steroid administration. This is the first documented report of the efficacy of oral chlorambucil in the treatment of primary uveal lymphoma.

Highlights

  • Ocular lymphomas account for five to 10 percent of all extra-nodal lymphomas

  • In all, 61 to 80 cases of primary uveal lymphoma have already been described in the literature

  • It is an indolent tumor with a good prognosis

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Summary

Conclusions

To the best of our knowledge this is the first documented report of efficacy of oral chlorambucil in treatment of a case of ILU. Consent Written informed consent was obtained from the patient for publication of this report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal. Competing interests The authors declare that they have no competing interests. Authors’ contributions IRK was responsible for the clinical management of our patient and preparation of the first draft of the manuscript. JK supervised the treatment of our patient and revised the manuscript. MS performed the literature search and revised the manuscript. The manuscript was prepared without the help of professional medical writers. All authors approved the final version of the manuscript

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