Reference | Onset of kidney symptoms after the primary diagnosis | Blood analysis | Number of patients with Renal autopsy/biopsy, histology (%) | Outcome | |||
---|---|---|---|---|---|---|---|
A. Autopsy Findings of Renal Involvement in MF Patients | |||||||
Swaminathan 2002 [8] | Case 1 (3y): proteinuria, erythrocyturia, AKI; Case 2 (7y): proteinuria, erythrocyturia, leukocyturia, granular cylinders, AKI | Case 1: thrombocytopenia, hyperbilirubinemia, progressive azotemia; Case 2: creatininemia | Case 1: scant interstitial lymphocytic infiltrate with preserved renal architecture; Case 2: complete replacement of renal parenchyma by atypical lymphocytes of variable size | Lethal | |||
Long 1974 [7] | Not reported | Eosinophilia, lymphocytosis or monocytosis | 2/15 (13), not reported | Lethal | |||
Rappaport 1974 [10] | Not reported | Not reported | 14/45 (31); tumour nodules, an interstitial infiltration with preservation of architecture, tumour cells in tubular epithelium et Bowman’s capsule | Lethal | |||
Epstein 1972 [21] | Not reported | Not reported | 23/96 (24), not reported | Lethal | |||
Cyr 1966 [22] | Not reported | Not reported | 5/23 (22), not reported | Lethal | |||
Block 1963 [9] | Not reported | Uremia, elevated BUN | 4/17 (23), nodular lymphomatous infiltrates | Lethal | |||
B. Renal Biopsy findings Kidney-involvement of MF | |||||||
Kairouani 2012 [3] | At the time of diagnosis; nephrotic syndrome | hypoalbuminemia, thrombocytopenia,creatininemia et uraemia | Not reported | Unrelated comorbidities | |||
Cather 1998 [15] | Case 1 (15 mths): hematuria, proteinuria. Case 2 (12 mths): proteinuria | Case 1: decreased hgb, thrombocytopenia, creatininemia; Case 2: creatininemia | Case 1:focal segmental and to a lesser extent global glomerular sclerosis, tubule atrophy, diffuse lymphocytic inflammatory infiltrates; Case 2: segmental and global glomerular sclerosis, proliferation of mesangial matrix, tubule atrophy, focal interstitial monocytic infiltrates and arteriosclerosis | Stabile | |||
Torrelo 1990 [12] | 5 y, nephrotic grade proteinuria, erythrocyturia, hyaline, granular and fatty cylinders | creatininemia, uraemia, hypoproteinemia | Uneven mesangial matrix proliferation with mesangial space deposits | Stable | |||
Allon 1988 [11] | 3 mths, nephrotic proteinuria, leukocyturia, erythrocyturia, granular hyaline urine cylinders | Trace SC, creatininemia, hypoalbuminemia, thrombocytopenia | Mesangial hypercellularity, interstitial infiltration of atypical lymphocytes | Not reported | |||
Averbuch 1984 [13] | 3 w,proteinuria, leukocyturia, erythrocyturia, granular cylinders, | increased hematocrit; creatininemia, BUN hypoalbuminemia | No glomerular changes, extensive interstitial edema with mixed lymphocytic infiltrate including eosinophils and plasma cells, tubular dilatation, focal degeneration, and necrosis of proximal tubule cells | Stabile | |||
Ramirez 1981 [14] | Case 1: at diagnosis; hematuria, leukocyturia. Case 2: 3 y; proteinuria, erythrocyturia, leukocyturia | Case 1: creatininemia and BUN; Case 2: leukocytosis, creatininemia and BUN | Mesangial proliferation | Not reported |