U05-19226. Clinical History ID - 94 yo M PMHx – remote IHD with CABG in 1980. HTN. Active and living independently prior to presentation Sept 22/05 at.

Slides:



Advertisements
Similar presentations
U # month history of being unwell Vasculitic lesions on lower limbs ANCA positive Likely Wegener’s vs MPA.
Advertisements

U # y.o. male ARF Creat 350 RBC casts + Active urine sediment.
PLASMA CELL DYSCRASIAS Monoclonal gammopathy of uncertain significance (MGUS)  Idiopathic  Associated with other diseases (autoimmune, infectious, non-heme.
Glomerular Diseases Dr. Atapour Differential diagnosis and evaluation of glomerular disease.
Case D 1 Age 37 M HIV for 17 years 1 week history of diarrhoea and fever Abrupt onset of oedema and oliguria Homosexual Teenage drug abuse.
Diabetic Nephropathy Yiming Lit, M.D. May 5, 2009.
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.
U Lupus.Nephrotic syndrome now. Normal creat.  C3/C4, ANA +, ? Membranous ?antiphospholipid Ab syndrome.
Understanding Your Blood Work
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.
Director of Scientific Affairs
U # Renal failure in Scotland Biopsy x2 with different diagnosis Now dialysis dependent with urine output (N) Kidney on U/S ?viable tissue.
Patient developed acute and chronic renal failure in 1999 associated with a renal stone. History, and a diagnosis of chronic pyelonephritis. She was started.
Clinical interpretation of Serum Free Light Chain assays 22 Feb 2013 Dr. Eric Chan Consultant Immunologist Queen Mary Hospital Hong Kong.
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.
U # ↑ SG 300. Proteinuria, Vasculitis rash. Native (L) Kidney.
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 # yo male,ARF (cr~300) RBC casts ++ %g/day proteinuria PANCA +ve.
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) 
Justin A. Crocker.  1 of the monoclonal gammopathies  Neoplastic proliferation of immunoglobulin producing plasma cells (single clone), often resulting.
Laboratory Handling of the Renal Biopsy Dr. Issam Francis Kuwait 4 th SSN Annual International Conference, Riyadh, April 2009.
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.
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.
Myeloma and the Kidney Ryan Sanford How Often is the Kidney Involved Symptomatic MM: CRAB – hyperCalcemia – Renal dysfunction – Anemia – Bone.
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.
상복부 통증을 주소로 내원한 46 세 여자 환 자 연세대학교 원주의과대학 원주기독병원 소화기내과, 1 병리과 석기태, 김재우, 조미연 1, 김현수.
Dr.Ruba Nashawati. Diabetes  Leading cause of ESRD  30% 40%  DN  DN Risk type I = type II.
M. Multiple Myeloma Malignant proliferation of plasma cells. Malignant proliferation of plasma cells. Normal plasma cell form Ig which contain heavy and.
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.
Department of Nephrology Hypercalcemia R4 Song Se-bin.
U # LRD kid tx March/99 Original Dis IgA.
Fig. 2(5) Eosinophilic IgD crystals in tubules Immunoglobulin D (IgD) Multiple Myeloma with Rapidly Progressing Renal Failure Dr. Modi. J, Dr. Eter. A,
AN UNUSUAL CASE OF MULTIPLE MYELOMA
Acute Kidney Injury (AKI)
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.
U # y.o. male Hemoptysis, pulmonary haemorrhage
U # /121 Cad Tx 14/05/2004 Creatinine early December US normal.
U
U # year old female Artheritis with increased creatinine, proteinuria, hematuria. ? Lupus.
U
Comorbidity NASH/HCV and HCC
Surgical Grand Rounds 12/9/13
Acute Kidney Injury - Mini Lecture
Mastocytosis.
IgA Nephropathy Southwest Nephrology Symposium February 24th 2018.
Quiz page: February 2002 American Journal of Kidney Diseases
Quiz Page Answers May 2006 American Journal of Kidney Diseases
Presentation transcript:

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 Panoka Hospital. Baseline Cr 100 June 2005 Sept 22/05- admitted with GI complaints – hydrated, but then actively diuresed. Treated with 3 antibiotics: Biaxen, Cefazolin and Cipro. On ACEI. First elevated urea Sept 29 at 30.7, with Cr 533 Oct 1. Oliguiric with no further response to high dose Fureosemide. Transferred to UAH Oct 4 with Cr 819 with elevated K and fluid overloaded. Dialysis initiated Oct 7. Progressively anuric until last 5 days when urine output increased in response to diuretic challenge.

Investigations: U/A - +1 ptn, +3 hgb, 2+ leuks. ++WBC and RBC. No eosinophils Hgb 85 PTH 42. Ca 1.58 PO Alb 29 Serologies negative. Normal compliments. CRP 70 24hr urine for protein 1.9 g/l. SPEP negative. Urine PEP – Kappa Chains Skeletal survey negative BM Bx – 14% plasma cells

LM

IF IgG, IgM, IgA: negative C3 : moderate punctate mesangial staining C1q negative Kappa: strong hyaline changes in tubular cytoplasm Lambda : negative Fibrin : moderate interstitial staining Albumin : negative

C3

Kappa

Fibrin

Diagnosis Light chain cast nephropathy with tubular injury consistent with kappa light chain disease