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PROF DR K H NOOR UL AMEEN M5 UNIT DR.RAKESH PINNINTI CASE OF JAUNDICE

A Case of Atypical Hemolytic Uremic Syndrome

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Page 1: A Case of Atypical Hemolytic Uremic Syndrome

PROF DR K H NOOR UL AMEEN M5 UNIT

DR.RAKESH PINNINTI

CASE OF JAUNDICE

Page 2: A Case of Atypical Hemolytic Uremic Syndrome

Chief complaints

30yr old male Mr.Vishwanathan was admitted withChief complaints of 1) jaundice 2) vomiting 3) fatigue 4) Oliguria Patient had above complaints for 4 days prior to admission

Patient was having altered sensorium since 6hr prior to admission

Page 3: A Case of Atypical Hemolytic Uremic Syndrome

Presentation

Patient was apparently doing well 4 days back when he noticed & was also alerted by his family …about yellowish discoloration of his eyes

It was sudden onset, persistent, progressive severity.

He noticed similar discoloration on his tongue, palms & soles the next day.

He felt fatigued, unable to work, rested for the most of the day.

Patient felt nauseated for most part of the day, with reduced appetite, vomiting 3 episodes/day since day of onset of jaundice

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Presentation

No H/O fever, diarrhea, abdominal pain,No H/O chest pain, palpitations, dyspnea, coughNo H/O headache, seizures, LOC, syncope/pre-

syncopeNo H/O recent blood transfusions, contact with

jaundiced person, No H/O malena, hemetemesis, easy bruising/

bleeding from any orifice.No H/O myalgia, arthralgia, skin rashes, mouth

ulcers, weight loss H/O reduced urine output since the day of onset

of jaundice.H/O passing high colored urine.

Page 5: A Case of Atypical Hemolytic Uremic Syndrome

History

Past History No H/O similar complaints in the pastNo H/O prior hospitalization, surgeries, drug

intakeNot a K/C/O DMT2, SHT, TB, malignancyPersonal HistorySmoker since 10yr Alcoholic since 8yr H/O alcohol binge in recent

weeks, last consumption 5 days prior to admission.Family HistoryNo similar complaints in the family

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Examination

Patient a adult male aged 30yrs moderately built & nourished.

Conscious, mild disoriented, disinterested in surrounding, looks distressed, afebrile, responding to oral commands & obeys commands, moves all 4 limbs spontaneously.

Vitals Pulse rate 102/min regular. BP 180/110 temp afebrile RR 24/min

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GPE

Pallor ++Icterus ++Puffiness of faceBPPENo clubbing No cyanosisNo lymphadenopathyNo petechiae, ecchymoses, bleeding from

orifices.No elevated JVPNo features of chronic liver disease/ liver failure.

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Systemic examination

Cardiovascular : S1 S2 heard , flow murmurs +

Respiratory : NVBS heard in all lung fields,

inspiratory crepts in B/L lung bases

Per abdomen: soft, no tenderness, liver palpable 2 cm below costal margin, no spleenomegaly, no free fluid, BS normal

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CNS

HMF : Conscious, mild disoriented, disinterested in surrounding, looks distressed, afebrile, responding to oral commands & obeys commands, moves all 4 limbs spontaneously.

CRANIAL NERVES : Normal

SENSORY & MOTOR : Normal

Cerebellar signs : NIL

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List of problems

Alcohol abuse Jaundice, anemia, edemaOliguriaHypertensionInspiratory creptsHepatomegalyAltered sensorium

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Investigations

CBCHb 8.0 gm% TC 8200 mm3DC P65 L32 E3ESR 8/16Plt 95,000 mm3• RFTUrea 10.4 gm%Creat 4.8 gm% URINE ROUTINEALBUMIN +RBC NILDEPOSITS 2-4 EP/mm3

LFT TB 6.5 IB 5.1 SGOT 54.2 SGPT 23.5 ALP 65.0 TOTAL PROTEIN 5.5 ALBUMIN 3.6• RETIC -3.5%• LDH -1736 U/L• DAT -VE

PERIPHERAL SMEAR : MACROCYTIC ANEMIA URINE FOR HB : POSITIVE24HR URINARY PROTIEN : 100 mg%

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Investigations

MP QBC : NEGATIVE MSAT : 1+ PT T 12 sec C 11 sec APTT T 25.2 sec C 27 sec INR 1.1 BT/CT N URIC ACID 9.9 gm% CA2+ 10.5 PHOS 9.6

ANA RF ASO APLA NEGATIVE CRP POSITIVE FDP MILDY ELEVATED (1.4 U) PROTIEN C & S N/A HIV, HBsg, HCV, HAV NEGATIVE STOOL C/S NEGATIVE BLOOD C/S NO GROWTH URINE C/S NO GROWTH

USG ABDOMEN : FATTY LIVERXRAY CHEST : NORMALECG : SINUS TACHY`

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RFT PROGRESSION

14/5 15/5 17/5 20/5 21/5 22/5 24/5 26/5 Date

104 96 148 180 99 89 179 71 Urea

4.8 4.9 5.2 13.0 8.8 6.7 8.2 7.2 Creat

Hemo-Dialysis started on 16/5/2011

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GH HEMATOLOGY FOR RESCUE

Hb 7.4gm%Tc 8,400DC P62 L22 B4 M6 normoblasts 6ESR 48/100Plt 1.1P.smear : microcytic hypochromic RBC normoblasts macrocytes polychromasia fragmented RBCs ++

IMP : TTP/HUS sug. BMA

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KIDNEY BIOPSY (Apollo)

Page 16: A Case of Atypical Hemolytic Uremic Syndrome

ONLINE REFERENCE

Fibrin thrombi & RBC in renal capillaries

Subintimal fibrin, but no inflammation

Healing from prior fibrinoid injury, occluding vessel

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Page 18: A Case of Atypical Hemolytic Uremic Syndrome

FINAL DIAGNOSIS

ATYPICAL HEMOLYTIC UREAMIC SYNDROME / D-HUS

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TTP vs HUS

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D+ vs. D-

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Oklahoma TTP-HUS Registry

Idiopathic — 37 % Drug-associated — 13 % Autoimmune disease — 13 % Infection — 9 %Pregnancy/postpartum — 7 %Bloody diarrhea prodrome — 6 % Hematopoietic cell transplantation — 4 %

Suspected TTP-HUS

Idiopathic TTP-HUS

Severe ADAMTS13 deficiency

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Disseminated intravascular coagulation is not typically present, but may be seen when there is diffuse tissue ischemia.

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Treatment

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Prognosis

Index contains three adverse prognostic factors (age >40, hemoglobin <9 g/dL, temperature >38.5ºC).

Subjects with zero, one, two, or all three of these adverse factors had 6-month mortality rates of 12, 14, 31, and 62 percent, respectively.

Atypical hemolytic–uremic syndrome has a poor prognosis, with death rates as high as 25% and progression to end-stage renal disease in half the patients

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THANK YOU