Primary Pleomorphic Mantle Cell Lymphoma of Kidney: A Case Report

Abstract

Introduction: Primary renal lymphoma (PRL) is rare while secondary involvement of the kidney by lymphoma is not infrequent. All morphologic varieties of lymphoma can involve kidney. The most common reported PRL is large B cell lymphoma. To our knowledge no prior case of primary renal mantle cell lymphoma (MCL), pleomorphic variant, has been reported. Case Presentation: A 67-year-old male presented with right flank pain. On examination a right sided abdominal mass and a unilateral varicocele were detected. On imaging studies there was a large mass of right kidney without nodal or other organs involvement. He underwent right nephrectomy. On gross pathological evaluation, a deformed kidney which was almost totally involved by tumor with hemorrhagic nodular cut surfaces was identified. Histologic evaluation and immunohistochemistry (IHC) staining followed by fluorescence in situ hybridization (FISH) study for t (11; 14) (q 13; q 32) / CCND1 -IGH confirmed diagnosis of MCL, pleomorphic type. Finally the patient was admitted in another hospital for continuing the treatment and received chemotherapy there. After one year of initial diagnosis the patient is still alive. Conclusion: The aim of this manuscript was to highlight a possible presentation of primary MCL, pleomorphic variant.

Lymphomatous interstitial nephritis coexistent with paraneoplastic crescentic membranoproliferative glomerulonephritis in a case of mantle cell lymphoma

“…[ 3 4 5 6 7 8 9 10 11 12 ] LIN due to MCL has been observed in 4 cases. [ 13 14 15 16 ] The coexistence of LIN and p-GN due to MCL is extremely rare. Till date, only 4 of these cases have been reported globally [ Table 1 ].…”