2021
DOI: 10.1136/bcr-2020-238153
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Proliferative glomerulonephritis and mantle cell lymphoma: a rare association

Abstract: Renal involvement in mantle cell lymphoma (MCL) is rare. We present the case of a man followed for MCL presented with acute kidney injury and positive antineutrophil cytoplasmic antibody (ANCA) type anti proteinase 3 (PR3). He was treated as for a rapidly progressing glomerulonephritis with cyclophosphamide and methylprednisolone followed by oral prednisone. Renal biopsy revealed diffuse endocapillary proliferation and segmental extracapillary proliferation in four glomeruli. Immunohistochemistry confirmed the… Show more

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Cited by 3 publications
(7 citation statements)
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“…The overall findings of this clinicopathologic cohort are well-supported by previous case reports of patients with MCL and kidney biopsies (summarized in Table 3 ). Of 15 previously reported cases of MCL-associated kidney injury, 9 had a polyclonal IC mediated GN, 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 usually with deposition of IgG, IgM, C3, and C1q. Two had C3GN, 24 , 25 1 had a pauci-IC crescentic GN, 26 9 had direct parenchymal infiltration by MCL, 17 , 18 , 19 , 21 , 22 , 23 , 24 , 26 , 27 and 2 had a proliferative GN without further available description of IC findings.…”
Section: Discussionmentioning
confidence: 99%
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“…The overall findings of this clinicopathologic cohort are well-supported by previous case reports of patients with MCL and kidney biopsies (summarized in Table 3 ). Of 15 previously reported cases of MCL-associated kidney injury, 9 had a polyclonal IC mediated GN, 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 usually with deposition of IgG, IgM, C3, and C1q. Two had C3GN, 24 , 25 1 had a pauci-IC crescentic GN, 26 9 had direct parenchymal infiltration by MCL, 17 , 18 , 19 , 21 , 22 , 23 , 24 , 26 , 27 and 2 had a proliferative GN without further available description of IC findings.…”
Section: Discussionmentioning
confidence: 99%
“…Of 15 previously reported cases of MCL-associated kidney injury, 9 had a polyclonal IC mediated GN, 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 usually with deposition of IgG, IgM, C3, and C1q. Two had C3GN, 24 , 25 1 had a pauci-IC crescentic GN, 26 9 had direct parenchymal infiltration by MCL, 17 , 18 , 19 , 21 , 22 , 23 , 24 , 26 , 27 and 2 had a proliferative GN without further available description of IC findings. 31 , 32 These case reports span 20 years and include a variety of lymphoma treatment approaches.…”
Section: Discussionmentioning
confidence: 99%
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“…Several case reports have been published on the glomerular involvement of MCL. Some of the histopathological findings include minimal change disease (MCD) ( 9 ), membranoproliferative glomerulonephritis (MPGN) ( 10 ), proliferative glomerulonephritis ( 11 ), and ANCA-associated pauci-immune crescentic glomerulonephritis ( 12 ).…”
Section: Discussionmentioning
confidence: 99%