HEMATOLOGY Flashcards

1
Q

FATIGUE JAUNDICE BACK PAIN DARK URINE
ACUTE HEPATITIS
ACUTE HEMOLISIS
HEMOLYTIC ANAEMIA
G6PD DEFICIENCY
HEREDITARY RED BLOOD CELL MEMBRANE DEFICIENCY WITH ASSOCIATED INFECTION
CHOLANGITIS TO RETAINED STONES IN THE COMMON BILE DUCT

A

IWU:

CBC
PERIPHERAL SMEAR
PT AND PTT
LFT
UA
US ABDOMEN

IM:
U FOR HEMOSIDERINE AND HEMOGLOBIN
HAPTOGLOBINA
G6PD LEVEL REPEAT AFTER HEMOLISIS IS OVER
COOMB TEST
CRYSTAL VIOLET STAIN OF PERIPHERAL SMEAR HEINZ BODIES

FM:
SUPPORTIVE CARE
HYDRATION
SUPPORT TRANSFUSION IF NEEDED

FU:
G6PD LEVEL RE CHECK

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2
Q

NOSE BLEED

THROMBOCYTOPENIA

VWD
ITP*
ACUTE LEUKEMIA
DRUG RELATED

DXZ

ISOLATED PLATELET
SLE
HIV
LLC

PATH:
IgG C3-5 SPLENIC DESTRUCTION

100-50 NOTHING
-50 STEROID IT
-10 IVIG IT ——–
AVOID PLAT TRANSF

A

IWU:

CBC*
PT
PTT
Fb

FM:

BMBx
ANA
HIV
ANTI PLATELETS Abs*
AUS

FU:

STEROID 4-6 wk
IVIG* IF THREATENING BLEEDING
SPLENECTOMY*
CITOTOXIC LIKE VINCRISTINE

THROMBOPOYETICS* NOT ONLY DESTRUCTION BUT MEDULLA
ROMIPLOSTIN
ELTROMBOPAG

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3
Q

SOB + JOINT BACK PAIN

ACS*
P INFARCTION OR PNA

A

IWU:

CBC
PERIPHERAL SMEAR 
BILI
UA
ABG
CXR

IM:

SPUTUM CYTOLOGY
URINE CYTOLOGY
Hb ELECTROPHORESIS
AGGRESSIVE PAIN MGMT W/NARCOTICS
HYDRATION
OXYGEN THERAPY
EMPIRIC ABx CETRIAXONE or CEFOTAXIME 
EXCHANGE TRANSFUSION*
IF HYPOXIA DOES NOT CORRECT WITH SUPPLEMENTAL MEASURES 
HYDROXYUREA FUTURE CRISIS

FU:

PNEUMOCOCCAL VACCINE
FOLATE CHRONICALLY

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4
Q

BLEEDING
HOSPITALIZED PNA BROAD SPECTRUM ABx*
COFFEE GROUND EMESIS

PT 16 RV <14
PTT 45 RV <35
PLAT 250

ALGORITHM DX:
PT - PTT OR BOTH*?
MIXING CORRECT?

FACTOR INHIBITOR AUTOIMMUNE DZ OR HEMOPHILIA MULTIPLE DOSES OF CRYOPRECIPITATE DEVELOP IMMUNITY

FACTOR DEFICIENCY
DIC
LIVER DISEASE
VITAMIN K DEFICIENCY*

A

IWU:

ASAT
ALAT
Fb
LDH
PAL
BIL

IM:

TRIAL OF S/C VIT K*
FFP

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5
Q

SHOCK/BLEEDING

POST TRANSFUSION STATE

A

IWU:

CBC
PT
PTT
Fb
UA
BUN /Crea

IM:

FREE Hb IN PLASMA
U Hb
HAPTOGLOBIN
COOMBS
LDH
BLOOD RE* TYPE PT &amp; DONOR
FM:
DIC=  FFP + SUPPORT MEASURES
RENAL FAILURE = FOROSEMIDE AND MANITOL 

FU:
BUN / Crea IF RAISES = DYALISIS
HYPOTENSION = IVF + DOBUTAMINE

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6
Q

EPISTAXIS AND BRUISING
MENINGOCOCCEMIA

DIC*
LEUKEMIA WITH RESULTANT INFECTION AND THROMBOCITOPENIA
LIVER FAILURE COAGULOPATHY
SEPSIS WITH ASSOCIATED THROMBOCITOPENIA

Pg -> PlASMIN Fg -> FIBRINA FIBRIN SPLITS PRODUCTS & D DIMER

A

IWU:

CBC
PT
PTT
LFT

IM:

Fb
FIBRIN SPLIT PRODUCTS
ABX TO CONTROL INFECTION
FFP REPLACEMENT
HEPARIN IS NOT INDICATED

FM:
TREAT THE CAUSE EX ABRUPTIO PLACENTAE

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7
Q

ROUTINE OFFICE VISIT
TINGLING IN HANDS AND FEET

DZ X

MGUS*
SPIKE < 3g OTHER POLICLONAL GG TENDS TO BE NORMAL PLASMA CELL BMBx < 10 %
MM Ca BUN/Cr MONOCLONAL SPIKE IgG IgA
HIV
SENSORY NEUROPATHY SECONDARY TO DRUGS EX ALCOHOL
VITAMIN B 12 DEFICIENCY

*SENSORY MOTOR NEUROPATHY

A

IWU:

CBC
TOTAL PROTEIN* > 9.5G/L ALB 3.5 G/L
ELECTROPHORESIS OF PROTEIN*
MONOCLONAL SPIKE IN THE GAMMAGLOBULIN SITE OF 2.5 G  
VITAMIN B12 LEVEL
LUMBAR PUNCTURE
IM:
SKELETAL SURVEY
URINE FOR BENCE JONES
BONE MARROW EXAMINATION

FU:

PROGRESSION TO PLASMA CELL DYSCRASIA RATE 10 Y 5 - 22%
MELPHALAN PREDNISONE BORTEZOMIB LEFLUNOMIDE OR CHT AGENTS HAS NOT PROVEN BE OF BENEFIT.

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8
Q

FATIGUE UPPER RECURRENT RESPIRATORY INFECTIONS AND EASY BRUISABILITY

APLASTIC ANEMIA
MYELODYSPLASIA
VITAMIN B 12 OR FOLATE
PNH
DRUG OR TOXIN INDUCED BM FAILURE
MYELOFIBROSIS
HYPERSPLENISM
HAIRY CELL LEUKEMIA
SLE
A

IWU:

CBC: WBC 1.2 Hb 7.8 PLAT 30
PERIPHERAL SMEAR
ABSOLUTE NEUTHROPHILE* COUNT IF < 500 WORRISOME - ABx IT
HIV 
CXR
BONE MARROW

IM:

URINE FOR HEMOSIDERIN
CYTOGENETICS
VITAMIN B 12 LEVEL

FM:

REMOVAL OF OFFENDING TOXIN IF PRESENT

BONE MARROW TRANSPLANTATION IN THOSE YOUNGER THAN 50 YO WITH A MATCHED DONOR

TRIAL OF INMUNOSUPRESSIVE THERAPY WITH ANTHYMOCYTE GLOBULIN AND CYCLOSPORIN IF TRANSPLANT IS NOT AN OPTION

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9
Q

FATIGUE DEPRESSION AND ATAXIA

VIT B12 
SYPHILIS TERTIARY
CEREBRO VASCULAR DISEASE
THYROID HYPO* OFTEN CO EXIST
CHRONIC ALCOHOLISM
DEPRESSION
A

IWU:

CBC -  MCV 102
THYROID: ANTI PER-OXIDASE / THYROGLOBULIN
TSH, FREE T4
LP
CT SCAN 
BUN/Crea

IM:

SERUM B12 / MMA / FOLATE
SERUM GASTRIN
SCHILLING TEST*
BLUNTED 2ND PHASE = ACHLORIDIA OR INTESTINAL INJURY DUE TO MEGALOBLASTOSIS

FM:
ANTI PARIETAL LOW SPECIFICITY
ANTI INTRINSIC FACTOR F NEG LOW SENSITIVITY ONLY 74%

FU:
VIT B12 REPLACEMENT
CBC

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10
Q

ROUTINE OFFICE VISIT

A

IWU:
IM:
FM:
FU:

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11
Q

FATIGUE

DZ X

IRON DEFICIENCY*
FOLATE DEFICIENCY
VITAMIN B 12 
THALASEMIA
SIDEROBLASTIC LEAD ALCOHOL
SULFA INDUCED BONE MARROW SUPPRESSION

HEMOLITIC ANEMIA DUE TO DRUGS OR SLE
EX: 82-92/ COOMB + /RETIC >

MYELODYSPLASIA

SYND THALASEMIC
TARGET CELL
NORMAL IRON STUDIES
INCREASED HFETAL Y A2
>RBC NUMBER /MICRO/NORMAL RDW
2 GENES DELETED= NORMAL ELECTROPHORESIS
WHEN 3 OF 4 GENES ARE DELETED 
HEMOGLOBIN H B4 TETRAMER IN 3/4 GENES  DELETED
A

IWU:
CBC
MCV* 72 MICRO

IM:
SMEAR
PRUSSIAN BLUE SIDEROBLASTIC
RETICULOCYTES

FM:

FERRITIN NORMAL IN SIDEROBLASTIC
TIBC
SERUM IRON HIGH IN SIDEROBLASTIC

TX:
PO FERROUS SULFATE
SOME B6 RESPONSE IN SIDEROBLASTIC
VIT C

FU:
CONSTIPATION
RETICULOCYTES COUNT

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12
Q

I WANT TO BE CHECKED OUT FOR CANCER

PAP
SIGMOIDOSCOPY
COLONOSCOPY
FOBT

A
Yly X 3 YRS THEN e/3 Yr
e/3-5 Yrs
e/ 10 Yrs
e/Yr
Yrly
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13
Q

JAUNDICE

A

IWU:
IM:
FM:
FU:

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14
Q

BROAD SPECTRUM CLINIC CASE PRESENTATION

CUSHING OR ECTOPIC ACTH OAT CELL 
DIABETES
DEPRESSION 
AUTOIMMUNE JOINT COMPLAINTS RHEUMATOID ARTHRITIS DEGENERATIVE ARTHRITIS
LIVER DISEASE
RENAL FAILURE 
PAN HYPO PITUITARY /HYPOGONADISM 
GRANULOMATOUS DISEASE 
ALCOHOLISM 
SUPRA VENTRICULAR TACHYCARDIA

PHLEBOTOMY OCCASIONAL CHELATION

INFERTILITY LOSS OF LIBIDO AND MALAISE

MISSENSE CYS 286
1/220 COMMON
STAPH AUREUS, YERSINIA, LISTERIA INFECTIONS IRON CONSUMER ORGANISM
30% HEPATOMA

SECONDARY IRON OVERLOAD CHRONIC TRANSFUSIONS EX: MAJOR THALASEMIA

A

IWU:

CBC
BMP
OGT
ASAT 
ALAT
EKG / ECHO 2D 
FSH
LH
TESTOSTERONE
SERUM IRON 
TIBC
FERRITIN 
SATURATION TRANSFERIN

IM:

CYTOGENETIC HFE GEN

FM:

LIVER BIOPSY SPARED BY CYTOGENETIC
DETECTION OF HFE GEN IRON CONTENT PER WT LIVER BIOPSY CUTOFF 2000 x gr
PT CARDIAC Sx DEFEROXAMINE CHELATION
CAREFUL MONITORING FOR THE DEVELOPING OF CIRRHOSIS OR HEPATOMA

INTENSIVE PHLEBOTOMY
MAINTENANCE PHLEBOTOMY

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15
Q

POSTRANSFUSIONAL REACTIONS

MAJOR: ABO*
MINOR: LEWIS Kf Jk

DIC= FFP + SUPPORT MEASURES

IgA DEFICIENCY= EPI + STEROID NO IV HEMOLISIS WASHED RBC or IGA DEF PLASMA TRANSF

FEBRIL NON HEMOLITIC: RIGOR AND FEVER NO IV HEMOLISIS LEUCOCYTE REDUCED FILTERED RBC

A

WORK UP TRANSFUSION REACTION :

HAPTOGLOBIN
COOMB
FREE Px Hb
UA-U Hb
LDH
BP MONITORING HYPOTENSION*
BUN/Crea MONITORING ATN*
BILI
SMEAR SCHISTOCYTES
D DMIMER
Fb LOW
DDIMER
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16
Q

65 F YO

DZ X PTT ELEVATED

XLR O> , YOUNG
FACTOR VIII
FACTOR IX

FXI DEFICIENCY
FXII DEFICIENCY
F INHIBITOR
LUPUS ANTICOAGULANT

A

AUTOSOM RECESIVE/ JEWISH ASK / F XI ASSAY LOW /MIXING DOES CORRECT.
ASYMPTOMATIC PTT/ F XII ASSAY LOW / NO TX NEEDED / MIXING DOES CORRECT.

MIXING DOES NOT CORRECT / HIGH VOL REPLACE FACTOR
LUPUS ANTICOAGULANT / ANTI CARDIOLIPID
FP VDRL
LIFELONG WARFARIN 3-3.5 IF THROMBOPHILIA
NEVER BLEEDS
STEROID TO AUTOIMMUNITY
MIXING STUDIES DON'T CORRECT
17
Q

PNH

VENOUS ALMOST ALWAYS PORTAL THROMBOSIS

A

Hb IN U
SUGAR WATER TEST TO SCREEN
FLOW CYTOMETRY DECAY ACCELERATOR FACTOR TO RULE IN
SOME RESPONSE TO STEROID

18
Q

MYELODISPLASIA

MYELOFIBROSIS

DYSMIELOPOYETIC DISORDER SPECTRUM
ESSENTIAL THROMBOCYTOSIS POLICITEMIA VERA TO MYELODISPLASIA MIELOFIBROSIS LEUKEMIA

A

> 60 YO
MORPHOLOGICALLY ABNORMAL WBC
PRELEUKEMIA
TRANSPLANT IS CURATIVE

> 50 YO SPLENOMEGALY
WBC COUNT MAY BE NORMAL LOW OR ELEVATED
TEAR DROPS CELLS IN THE PERIPHERAL SMEAR
INCREASE RETICULIN FIBER IN MARROW