U06-10814 #831277720 Renal failure in Scotland Biopsy x2 with different diagnosis Now dialysis dependent with urine output (N) Kidney on U/S ?viable tissue.

Slides:



Advertisements
Similar presentations
Acute Glomerulonephritis
Advertisements

Sickle Cell Anemia Columbia County Medical Assistant Association.
Preliminary materials Practical Cytological and Histological Approach to Lymphoid Lesions Workshop 8, 55 th annual meeting Canadian Association of Pathologists.
بسم الله الرحمن الرحيم Medical mycology
+ Case Study One Pediatric Patient’s Experience Shelley Chapman RN, BSN, CCTC Children’s Hospital of Wisconsin.
What You Need to Know About Acute Chest Syndrome By Susan Hernandez, RN, CNN, BSN, and G. Elaine Patterson, RN-C, EdD, MA, Med, FPN-C Nursing2009, June.
Clinical History Locke : 55 yo male past medical history of hypothyroidism presents with increasing dyspnea. Patient was treated with several.
Diagnosis and Management of TB John Yates Consultant Infectious Diseases.
Case Discussion Dr. Raid Jastania. 19 year old female presents with fever and generalized lymphadenopathy for one month. What are the causes of Fever?
U Lupus.Nephrotic syndrome now. Normal creat.  C3/C4, ANA +, ? Membranous ?antiphospholipid Ab syndrome.
A 25 year old farmer with joint pain Laura Zakowski, MD* * No financial disclosures.
Unit 9 Diagnosis and Treatment of Paediatric TB: B Family Case Botswana National Tuberculosis Programme Manual Training for Medical Officers.
NYU Medical Grand Rounds Clinical Vignette Lucy Doyle MD, PGY-2 March 24, 2010 U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS.
國泰馬偕聯合病例討論會 R郭馨仁 Vs吳志仁. Basic datas Name: 蔡x峯 Age: 61 y/o Sex: female Chart no: Date of admission: Date of renal biopsy: (
HPI A previously healthy 33 year old male complaining of progressive nonproductive cough for 2 months. He became more short of breath with exertion in.
Patient developed acute and chronic renal failure in 1999 associated with a renal stone. History, and a diagnosis of chronic pyelonephritis. She was started.
NYU Medical Grand Rounds Clinical Vignette Phillip Joseph, MD, PGY-2 September 25 th, 2013 U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS.
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.
NYU Medical Grand Rounds Clinical Vignette Christopher Schultz, MD, PGY-2 February 24, 2010 U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS.
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.
How does the immunology relate to clinical medicine?
U # ↑ SG 300. Proteinuria, Vasculitis rash. Native (L) Kidney.
VILNIUS UNIVERSITY HOSPITAL SANTARISKIU KLINIKOS.
U yo African female student (here since 2001) Medical exam for Immigration notable for protein-uria and Hematuria. Serum Creatinine 81umol/L.
U # Creat 250 Nephritic urine ? Crescentic GN.
71-year old male Admitted with worsening shortness of breath PMHx: Severe COPD, A.Fib, CHF/ischemic, PE On long term anticoagulation with Pradaxa 150.
U # y.o. female with pneumonia  creatinine proteinuria very low C3, C4.
Glomerulonephritis Brian S. Pavey, DO, MS. Presentation Sudden onset – Hematuria – Hypertension – Edema – Acute kidney injury.
U # yo male,ARF (cr~300) RBC casts ++ %g/day proteinuria PANCA +ve.
Case Discussion Dr. Raid Jastania. What is the outcome of inflammation?
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.
U #009N Recurrent edema with most recent episode proteinuria with creat > 300.
Tropical Fevers Case 1: 27 year old woman comes to a local health unit with history of a gradual onset of fever and headache and loss of appetite over.
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.
November 26, HPI 14 month old male seen by PCP intially for fever and nasal congestion with purulent nasal discharge and cough. At initial visit.
Exacerbations. Exacerbations An exacerbation of COPD is an acute event characterized by a worsening of the patient’s respiratory symptoms that is beyond.
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 # 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.
Tubulointerstitial Nephritis and Uveitis (TINU) Syndrome Sana Khochtali Imen Ksiaa Anis Mahmoud Bechir Jelliti Department of Ophthalmology Fattouma Bourguiba.
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.
TID Case Nicole Theodoropoulos, MD, MS The Ohio State University.
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.
PRIMARY PULMONARY TB Clinical Features: (in children) No symptoms or signs and passes unnoticed in the majority of cases  characterized by 1ry lesion.
SATAN’S CURSE Saad Ghafoor MD (Associate), Saiprakash Venkateshiah MD, FCCP  Hyper Ig E syndrome or Job’s syndrome is a multisystem disorder that affects.
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.
A 23 year old Caucasian male presented with shortness of breath, hypertension, bloody sputum, and a history of drug abuse (confirmed by urinalysis). He.
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.
CASE 1: Management of metastatic disease in a resource-limited setting
A. Karki1, V. Patel2, K. Sherani3,J. Raynor3, K. Mandal3, A. Shalonov3 
53 yo female referred for elevated SCr (178 mmol/l, 28 ml/min) and change in symptoms….? connective tissue disease Dx of hypocomplementemic urticarial.
Miliary TB.
U # y.o. male Hemoptysis, pulmonary haemorrhage
U # /121 Cad Tx 14/05/2004 Creatinine early December US normal.
U # year old female Artheritis with increased creatinine, proteinuria, hematuria. ? Lupus.
Respiratory Disorders
U
Aspirated Foreign Body
Pneumonia in Children. What is pneumonia? Pneumonia is an inflammation of the lungs caused by bacteria, viruses, or chemical irritants. It is a serious.
COPD Exacerbations UCI Internal Medicine Mini-Lecture
3º Curso de Doenças Pulmonares Difusas – FMUP/HSJ
DIFFUSE ALVEOLAR HEMORRHAGE SYNDROM
Presentation transcript:

U # Renal failure in Scotland Biopsy x2 with different diagnosis Now dialysis dependent with urine output (N) Kidney on U/S ?viable tissue

Case Summary: ES 67 year old Caucasian female, retired school teacher and mother of 3 with significant past medical history of (1) ureteric surgery 1965; (2) G6P3 – 3 miscarriages between 2nd and 3rd child; (3) Ex- smoker – quit 20 years ago; previously smoked ½ pk/day for 10 years. HPI: Jan-March 2005: Traveled to Vietnam; developed severe diarrhea upon return to Canada; Blastocystis hominis; treated with Cipro for 1 month with resolution of diarrhea however next 6-9 months general health intermittently poor; malaise; fatigue; constitutional symptoms. Sept 2005: Traveled to Scotland to visit daughter (vet); URTI/pneumonia/treated with levoquine for 10 days; questionable interstitial fibrosis noted on CXR Dec 2005: presented to Dumfries hospital with SOBOEx/ fever/rash/wt loss

During admission in Scotland (Dec 2005 – May 2006), several findings: Hepatomegaly with transaminitis – liver biopsy – steatosis heart murmur noted; ?Q fever – treated with doxycycline x 10 d;serology negative Grp B strep isolated from throat swab – treated with amoxil for 10 d Bilateral pleural effusions and pericardial effusions - ?vasculitis started on steroids Mantoux positive but history of BCG vaccination CT scan showed mediastinal lymphadenopathy – biopsy reported on Feb 21/06 as MAC – treated with ethambutol/clarithromycin Opthamology consulted re screening pre-ethambutol – dx retinal vasculitis Temporal aa bx – negative; bone marrow biopsy negative; blood cultures negative; viral serology negative; autoantibodies negative

March 2006: tap of pleural effusion – transudate; renal function noted to be declining; clarithromycin d/c and azithromycin started; renal dosing of ethambutol; noted to have 2 g/day proteinuria; steroid increased; thrombocytopenic (80 lowest) and MAHA (90 lowest) noted; renal biopsy #1 performed in Dumfries and renal biopsy #2 performed in Glasgow. Based on biopsy #1: treated with IV solumedrol/Cyph; based on biopsy #2: plasma exchange initiated. March 17, 2006: started on hemodialysis; rapid afib – started digoxin Rheumatology opinion: not scleroderma; MAC treatment d/c. May : 2nd pleural effusion tap: transudate. Transferred to UAH May 19, 2006 (treated with 10 weeks of steroids at this point). Issues while at UAH:

Renal failure – dialysis dependent; producing ~ cc/d with large doses of diuretics; MRI/MRA kidneys – normal size kidneys; extrarenal pelvis on Rt; all serology repeated and negative including ANCA, ANA antiphospholipid Ab and Anti SCL70, complements normal; June 1st renal biopsy. Viral serology repeated negative. Steroids being tapered. Pulmonary status – new airspace disease LLL; persistent L pleural effusion>R; CT chest – cardiomegaly; bilat pl effusions; LUL and LL ground glass opacification persistent; past granulomatous infection; echocardiogram June 14: no pericardial effusion; good wall motion; Lt pl effusion; bronchoscopy with BAL – negative; Bone marrow repeated June 2nd: negative culture; all antibiotics stopped; acute deterioration with hypoxia June 16th – no worsening of Lt pl effusion/ MAC a concern/ started on Pip/Tazo/Azith/Septra– U/s guided tap June 22 Neurologic status – CT head May 31 – small vessel ischemic changes; CT head for acute deterioration June 21 no change Persistent normocytic anemia; platelet count normal/high; MRSA nose and groin positive initially; now bacteremic from CVC; on vanco Depression – on Celexa; psychiatry following

IgG-negative IgA- negative IgM- mild mesangial staining C3- moderate peritubular capillary staining C1q-negative Kappa-negative Lambda-negative Fibrin- moderate interstitial staining Albumin- negative IF

IgM

C3

Fibrin

Diagnosis: Renal Biopsy: Thrombotic Microangiopathy in a relatively quiescent phase with few obvious thrombi.