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Renal  ` RENAL—PAthoLogy                                              Renal  ` RENAL—PAthoLogy        SeCTIOn III      597




                  Nephrotic syndrome     NephrOtic syndrome—massive prOteinuria (> 3.5 g/day)
                   Minimal change        Also known as lipoid nephrosis. Most common cause of nephrotic syndrome in children.
                    disease              Often 1° (Idiopathic) and may be triggered by recent Infection, Immunization, Immune stimulus
                                          (4 I’s of MCD). Rarely, may be 2° to lymphoma (eg, cytokine-mediated damage).
                                         1° disease has excellent response to corticosteroids.
                                             ƒ LM—Normal glomeruli (lipid may be seen in PCT cells)
                                             ƒ IF—⊝
                                             ƒ EM—effacement of podocyte foot processes  A
                   Focal segmental       Most common cause of nephrotic syndrome in African-Americans and Hispanics.
                    glomerulosclerosis   Can be 1° (idiopathic) or 2° to other conditions (eg, HIV infection, sickle cell disease, heroin abuse,
                                          massive obesity, interferon treatment, or congenital malformations).
                                         1° disease has inconsistent response to steroids. May progress to CKD.
                                             ƒ LM—segmental sclerosis and hyalinosis  B
                                             ƒ IF—often ⊝ but may be ⊕ for nonspecific focal deposits of IgM, C3, C1
                                             ƒ EM—effacement of foot processes similar to minimal change disease
                   Membranous            Also known as membranous glomerulonephritis.
                    nephropathy          Can be 1° (eg, antibodies to phospholipase A  receptor) or 2° to drugs (eg, NSAIDs, penicillamine,
                                                                             2
                                          gold), infections (eg, HBV, HCV, syphilis), SLE, or solid tumors.
                                         1° disease has poor response to steroids. May progress to CKD.
                                             ƒ LM—diffuse capillary and GBM thickening  C
                                             ƒ IF—granular due to immune complex (IC) deposition
                                             ƒ EM—“Spike and dome” appearance of subepithelial deposits
                   Amyloidosis           Kidney is the most commonly involved organ (systemic amyloidosis). Associated with chronic
                                          conditions that predispose to amyloid deposition (eg, AL amyloid, AA amyloid).
                                             ƒ LM—Congo red stain shows apple-green birefringence under polarized light due to amyloid
                                            deposition in the mesangium
                   Diabet ic glomerulo-  Most common cause of ESRD in the United States.
                    nephropathy          Hyperglycemia Ž nonenzymatic glycation of tissue proteins Ž mesangial expansion; GBM
                                          thickening and  permeability. Hyperfiltration (glomerular HTN and  GFR) Ž glomerular
                                          hypertrophy and glomerular scarring (glomerulosclerosis) Ž further progression of nephropathy.
                                             ƒ LM—Mesangial expansion, GBM thickening, eosinophilic nodular glomerulosclerosis
                                            (Kimmelstiel-Wilson lesions  D)

                                        A                    B                    C                   D



































          FAS1_2019_14-Renal.indd   597                                                                                 11/7/19   5:42 PM
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