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Interstitial nephritis associated with PostInfectious GN PRAET MARLEEN, MD, PhD UNIVERSITY HOSPITAL GHENT
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Clinical History: Background Man 53 year Ethyl ++, smoking 10-12 cigars/day 1994: T3N0M0 Spinocellular Carcinoma of the glottis 2007-2010: recurrent hemoptoe presenting a cystic lesion at the Right Upper Lobe of the Lung.
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Clinical History: Recent 04/10/2011: lobectomie Histology: Pachypleuritis met underlying scar of the pulmonary parenchyma. Bronchiectasy and chronic inflammation. No malignancy. Follow up: hydropneumothorax with infection: crp 15 mg/dL, WBC 19000 10^3/ µL, fever 39°C, sputum: H.Influenza
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Admission in Emergency 3 weeks after lobectomy Acute renal failure: - Creatinin 4,21 mg/dl - Proteinuria 4.3g/L - Macroscopic hematuria - Oliguria - WBC: 21700 10^3/ µL - CRP 10.6 mg/dl Normal temperature, normal BP Renal biopsy.
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AgMethanamine x 4 Kidney biopsy containing 30 glomeruli: 4 glomeruli are completely sclerosed. 7 glomeruli undergo proliferative changes with crescent formation surrounding the glomeruli segmentally or globally. Glomeruli, tubuli and interstitium are infiltrated by neutrophils. No vasculitis
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AG Methanamine x10
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CONGORED x25
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CONGORED X 10
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PAS x40
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Differential Diagnosis (Focal) crescentic glomerulonephritis post infection (PIGN). Microangiopathic vasculitis with crescentic glomerulonephritis: ANCA-associated systemic vasculitides (Wegener, microscopic polyangitis, Churg- Strauss) Sepsis with combined interstitial and glomerular changes.
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Immunofluorescence Findings Ig G, Ig A, Ig M, C1Q: negative IF findings Kappa, Lambda: negative IF findings C3: strong granular staining at capillary wall 3+ SUGGESTED DIAGNOSIS: Post infectious glomerulonephritis with crescent formation in < 50% of the glomeruli. IF findings consistent with previous infection.
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C3 Deposition at capillary wall
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ORIGIN OF INFECTION 2 possibilities: - Hydropneumothorax with infectious agent: H. Influenzae was found in the sputum. - Bronchiectasy with ulcerative inflammation and presence of germs: however no infectious agent was cultivated
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Treatment of the patient Original clinical diagnosis: vasculitis: plasmapheresis, cyclophosphamide, high dosed steroids. Creat levels up tot 6. 65 mg/dl. However: ANCA: negative, anti GBM: negative Switch of treatment after IF findings: stop plasmapheresis, stop cyclophosphamide: Instead: intravenous AB, steroids, dialysis. Creat level is decreasing with recovery of the patient.
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Discussion Glomerulonephritis and infection - is primarily a childhood disease occuring after upper respiratory infection(5-10 %) or impetigo (25%) (Streptococcus A, beta – hemolytic, serotypes 12, 49) - in older patients: less well known Male/female ratio 2.8:1 Immunocompromised background is present in 61 %, most often diabetes or malignancy Infectious agent most often found: staphylococcus (46%), streptococcus (16%) and unusual gram- negative organisms.
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Discussion Glomerulonephritis and infection: IF findings in PIGN: IgG and C3, or C3 only IgA dominant PIGN: strong association with staphylococcal infections of the skin with diabetes as a major risk. This variant of APIGN should be distinguished from the classic IgA nephropathy ( Haas M Human Pathology 2008, 39, 1309-1316, Nasr S, D’Agati Nephron Clin Pract 2011, 119, 18-26) EM findings: classical PIGN: large subepithelial deposits (humps). APIGN: often no subepithelial deposits with varied findings (subendothelial, mesangial). Our patient: NO glomeruli in EM material.
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DISCUSSION Glomerulonephritis and infection in our patient: no definite infectious agent revealed But “immunocompromised”: alcoholism NASR. ET AL.: Acute Postinfectious Glomerulonephritis in the Modern Era. Medicine, 87:21-32, 2008
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NASR. ET AL.: Acute Postinfectious Glomerulonephritis in the Modern Era. Medicine, 87:21-32, 2008 ‘In Western Europe, alcoholism had become the most important risk factor for Acute Postinfectious Glomerulonephritis’ Upper respiratory tract > skin > lung > endocarditis > teeth 56% complete remission 4-17% requiring renal replacement therapy ‘Evidence supporting the use of steroid therapy for postinfectious crescentic GN is largely anecdotal’
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