U # y.o. male Hemoptysis, pulmonary haemorrhage

Slides:



Advertisements
Similar presentations
Acute Glomerulonephritis
Advertisements

U # month history of being unwell Vasculitic lesions on lower limbs ANCA positive Likely Wegener’s vs MPA.
U # y.o. male ARF Creat 350 RBC casts + Active urine sediment.
Immune Complex Nephritis.
Glomerular Diseases Dr. Atapour Differential diagnosis and evaluation of glomerular disease.
U Clinical History ( ): Generalized decline in health since Feburary 2005 including: Wt loss/recurrent ‘Pneumonia’/ arthralgia and joint.
ISRTPCON and CME AIIMS NEW DELHI Sept,2013 Dr Kiran K Senior Resident, PDCC-Renal and Transplant Pathology Department of Histopathology PGIMER, Chandigarh.
Enzyme Case Studies: 1 A 67 year old male two days after sustaining multiple injuries in a motor vehicle accident complains of chest pain. There is no.
U Lupus.Nephrotic syndrome now. Normal creat.  C3/C4, ANA +, ? Membranous ?antiphospholipid Ab syndrome.
U y/o man with recent dx of HI +DM. creatinine increasing rapidly in 6 months. ACR low at 5.3, 2+ hematuria x 2-3 years with negative.
Patient developed acute and chronic renal failure in 1999 associated with a renal stone. History, and a diagnosis of chronic pyelonephritis. She was started.
U # y old female with PMH of mild RA, increased LFT, asthma, atypical chest pain, depression Presented late 2004 with chronic abdo.
U and U # U y.o. male ? Wegener’s.
U # yr old woman with sinusitis,arthritis pulmonary hemorrhage,microscopic hematuria Proteinuria 2.5g/day (+) pANCA,Cr 127 ANA(+). Anti.
U # y.o. male with increased proteinuria, arthralgia and lower limb petechial rash. Hypertension ? Renal vasculitis ? Henoch-Schönlein.
Idiopathic Pulmonary Fibrosis: Diagnosis and Understanding
U # ↑ SG 300. Proteinuria, Vasculitis rash. Native (L) Kidney.
Interstitial nephritis associated with PostInfectious GN PRAET MARLEEN, MD, PhD UNIVERSITY HOSPITAL GHENT.
U yo African female student (here since 2001) Medical exam for Immigration notable for protein-uria and Hematuria. Serum Creatinine 81umol/L.
U # Severe nephrotic syndrome with rising creatinine.
U # Creat 250 Nephritic urine ? Crescentic GN.
U # y.o. F New diagnosis of lupus Normal creatinine.
U # y.o. female with pneumonia  creatinine proteinuria very low C3, C4.
U DM with microhematuria. U yr married female,mother of two children, referred to the Renal clinic by family physician on january.
66 F PMH: HTN, Gout, DVT (Feb/06 and ? Sep/06) PMH: Heterozygous for Prothrombin mutation. FOCAL PROLIFERATIVE IMMUNE COMPLEX GN (toward chronic GN) 
U # year-old, born in India, has lived in Canada since Initially presented Feb 2003 with a Cr of ~ 300 (212 Sep 2002, 122 Dec.
And Review of Acute nephritis Syndromes. Karyomegalic Tubulointerstitial Nephritis  Symptoms: Recurrent Pneumonias Renal failure leading invariably to.
U #009N Recurrent edema with most recent episode proteinuria with creat > 300.
U y old female with PMH of mild RA, increased LFT, asthma, atypical chest pain, depression Presented late 2004 with chronic abdo pain, had.
U # yo Nigerian Canadian, born in Toronto HPI Presented with a several day history of intractable N&V, bilateral flank pain, fever and.
54 year old man with 7 grams/day proteinuria Microscopic hematuria and serum creatinine nearly 130. He is HCV positive and had received liver transplant.
U # ATN 1 year ago with recovery but now proteinuria with DM ?other diagnoses.
U # Proteinuria. 52 year old female followed for dextrocardia and Tetralogy of Fallot complicated by pulmonary hypertension and right.
U # Healthy young male 28 Y came in with bilateral flank pain Creat 155 went up to 286 Received solumedrol 1 gm last night Today’s creat.
U # Cad Tx 15 years ago Recent  creatinine with mild proteinuria No RAS.
U # IgG- strong coarsely granular capillary loop staining,mild to moderate granular peritubular staining IgA- moderate mesangial staining.
U Chronic renal failure secondary to ? Hepatitis C.
U # Kidney-pancreas transplant several years ago. Recent increase in creatinine with some proteinuria. Pancreas working well.
65 year old female with a h/o familial Mediterranean fever, diabetes, proteinuria (2.7 g), hematuria (20-30rbc’s) – no rbc casts on urinanalysis. Labs.
U # yr old woman with Serum Cr 202 Urine Pr/Cr 338 mg/mmol,elevated LFTs Weight loss No hematuria SPEP-polyclonal gammopathy (L) Native.
U Clinical History A 53 year old man who had very little or no medical care in the past, presents to ER with the only complaint of insomnia.
U # Chronic renal failure – secondary to IgA nephropathy. Deceased donor kidney transplant – August Complicated by delayed graft.
U History is that of a 12 y/o male presenting with a few day history of vomiting, facial swelling, fatigue and oliguria. Hypertensive only at.
사구체신염 진단 Tips 신장내과 임천규. Chang JH et al, Nephrol Dial Transplant 2009 Changing prevalence of glomerular diseases in Korean adults IgAN MN MCD FSGS MPGN.
U Clinical History ID - 94 yo M PMHx – remote IHD with CABG in HTN. Active and living independently prior to presentation Sept 22/05 at.
U # LRD kid tx March/99 Original Dis IgA.
A. Karki1, V. Patel2, K. Sherani3,J. Raynor3, K. Mandal3, A. Shalonov3 
Hepatitis Tutoring By Alaina Darby.
Nephrology Pathology Rounds Oct 21/05
53 yo female referred for elevated SCr (178 mmol/l, 28 ml/min) and change in symptoms….? connective tissue disease Dx of hypocomplementemic urticarial.
MICROBIOLOGY PRACTICAL
Table 1.2.1: Total number of renal biopsies by centres, 2005 – 2012
NEFROLOGISK KLINIK P, RIGSHOSPITALET
U # /121 Cad Tx 14/05/2004 Creatinine early December US normal.
Immune Complex Nephritis
U
U # year old female Artheritis with increased creatinine, proteinuria, hematuria. ? Lupus.
U
MICROBIOLOGY PRACTICAL
Primary biliary cirrhosis, cirrhotic stage
Glomerular pathology in systemic disease
Acute viral hepatitis type C
Chronic viral hepatitis type B and chronic delta
Alcoholic hepatitis with diffuse interstitial fibrosis
Chapter 14 Hepatic Tumors, Malignant 1
Primary biliary cirrhosis, AMA negative
Nephrotic Syndrome.
How to approach Hematuria How to approach Proteinuria Glomerulonephritis Overview Dr. Mohammad Alkhowaiter Consultant Nephrologist.
Quiz page: February 2002 American Journal of Kidney Diseases
DIFFUSE ALVEOLAR HEMORRHAGE SYNDROM
Presentation transcript:

U06-20612 #87734-4041 29 y.o. male Hemoptysis, pulmonary haemorrhage Active urine sediment Creat 1200 mol/L Serology pending

29 Yr old male, Pakistani descent past medical Hx 29 Yr old male, Pakistani descent past medical Hx ? Flu like symptoms – 4 days, then SOB, chest pain and hemoptysis. Admited to ICU Oct 27 – intubated for pulm Hge/ hypoxia/ resp failure bronchoscopy: diffuse alveolar Hge required 7 units of Blood Labs: s.Cr at presentation: 1274 µmol/l urine: 3+ ptn, 3+ Hb, +ve casts ptn/Cr : 514 mg/mmol ANCA, anti-GBM, anti DNA, HBsAg, HCV Ab, : are negative cryo : pending started on PRISMA in ICU biopsy…

IF IgG- Negative. IgA- Negative. IgM- Negative. C3- Mild vascular staining. C1q- Negative. Kappa- Negative. Lambda- Negative. Fibrin- Mild to moderate interstitial staining. Albumin- Negative.

C3

Fibrin

EM Will be ready in the coming weeks

Diagnosis Renal Biopsy: Probable chronic glomerulonephritis with extensive glomerulosclerosis and parenchymal scarring. Polymorph aggregates in collecting ducts suggesting ascending bacterial infection.

Comment Despite evidence of ascending bacterial infection, the most likely cause of disease is chronic GN. The changes seen in the 2 non-sclerotic glomeruli support the idea of primary glomerular disease. However, various glomerular changes would be expected with compensatory hypertrophy so one cannot completely exclude the possibility of primary tubulointerstitital disease.