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Clinical Images
143 (
2
); 251-252
doi:
10.4103/0971-5916.180235

Primary testicular plasmablastic lymphoma: unique case in a 30 year old

Department of Pathology, Lab Medicine & Transfusion Medicine, Medanta- The Medicity Hospital, Gurgaon 122 001, Haryana, India

* For correspondence: sachdev05@gmail.com

Licence

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

Disclaimer:
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.

A 30 yr old HIV-negative immunocompetent male presented with painful right scrotal swelling to Medanta - The Medicity, Gurgaon, India, in February 2014 (Figure A). The patient previously experienced a painful episode of left scrotal swelling four months ago for which he had consulted another hospital. There, left orchidectomy was done and diagnosed as plasmacytoma for which chemotherapy was started (adriamycin, bortezomib and dexamethasone). Now core biopsy of right testicular mass was performed which showed sheets of large lymphoid cells with prominent nucleoli and brisk mitosis (Figure B, C). Immunohistochemically, the cells were positive for CD45, CD138, CD56, epithelial membrane antigen and MUM-1; negative for CD20, CD3, CD30, cytokeratin, PAX-5, PLAP (placental alkaline phosphatase) and ALK (anaplastic lymphoma kinase CD246 ALK1). The tumour cells had high Ki-67 index (90%) (Figure DK). Diagnosis of plasmablastic lymphoma of testes was male; patient started on CHOP-E (cyclophosphamide, doxorubicin, vincristine, prednisolone and etoposide) chemotherapy. The patient received six cycles of chemotherapy with intrathecal methotrexate for CNS disease. His general condition was stable with reduction in tumour size during follow up for eight months.

(A). Clinical picture shows left orchidectomy with enlarged right testes. (B) Testicular core biopsy showing uniform population of large cells with round nuclei, coarse chromatin and prominent nucleoli (Hematoxylin and Eosin, 40x). (C) Testicular core biopsy showing areas of necrosis and inflammatory infiltrate (Hematoxylin and Eosin, 40x). Testicular biopsy showing plasmablastic lymphoma, tumour cells were positive (brown colour) for CD45 (D), CD138 (E), Ki-67 (F), EMA (G) (40x) and MUM-1 (H) (10x) and negative for CD30 (I), Cytokeratin (J) and PAX-5 (K) (10x) [DAB staining].
Figure
(A). Clinical picture shows left orchidectomy with enlarged right testes. (B) Testicular core biopsy showing uniform population of large cells with round nuclei, coarse chromatin and prominent nucleoli (Hematoxylin and Eosin, 40x). (C) Testicular core biopsy showing areas of necrosis and inflammatory infiltrate (Hematoxylin and Eosin, 40x). Testicular biopsy showing plasmablastic lymphoma, tumour cells were positive (brown colour) for CD45 (D), CD138 (E), Ki-67 (F), EMA (G) (40x) and MUM-1 (H) (10x) and negative for CD30 (I), Cytokeratin (J) and PAX-5 (K) (10x) [DAB staining].

Acknowledgment

The authors acknowledge Drs Ishani Mohapatra, Consultant-Pathology, Smeeta Gajendra, Associate Consultant and Sunil Kumar Gupta, Associate Consultant-Medical Oncology for their significant and valuable contributions.


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