Hematology Flashcards

(47 cards)

1
Q

(Age)* 67y + wt loss + FAHM + night sweeting +hoarseness of voice + CXR show opacity in the rt upper mediastinum + spenomegly +hepatomegly +no hx of dysnea or smoking
Most appropriate invest ?

A
*dx : lymphoma 
Tissue diagnosis is the most definitive way 
So.do LN biopsy 
# Just for recall 
Mediastnium Lns ddx : 
* TB 
*Sarcoidosis
*Non_Hodgkin Lymphoma 
*bronchogenic carcinoma
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2
Q
FAHM +night sweeting + diagnosed with Hodgkin lymphoma
#Type of cell is associated with itb?
A

Reed_Sternberg cells

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3
Q

HIV +ve + loss of wt +night sweeting + peripheral lymphadenopathy + splenomegly

A

Non Hodgkin lymphoma

🇦🇱 NHL more assosiated with HIV than HL (Hodgkin lymphoma )

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4
Q

Hx of travel from Newyork to UK + wt loss +night sweeting + cervical lymphadenopathy
Most appropriate dx ?

A

Lymphoma

🇦🇱👻 u should be able to differentiate bet TB &lymphoma

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5
Q

TB
1_ hx of travel to south Asia or south Africa
2_ FAHM
3Hilar ,paratracheal LN ,superficial nodes involved
4Firm ,tender,discrete .
5
chronic productive cough with purulent +-blood stained sputum
6
erythema nodosum

A
Lymphoma 
1_ hx of HIV🤔
2_ FAHM 
3_LN in the lower neck &supreclavicular LN 
4_ painless, rubbery 
5_chest discomfort with cough &dysnea 
6_ splenomegly,hepatomegly,SVC ,bone .
7_mediastnium masses are frequent
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6
Q

28w pregnant + HB :11 🤔

A
Normal physiological anemia (dilutional)
Limits of anaemia in pregnancy 
*<11 in 1st trimester 
*<10.5 2nd &amp;3rd tried 
*<10 postpartum period 
📢📢hematological changes in pregnancy :
*inc. Plasma vol.
*inc. Erythropoetin 
* MCV/MCHC unaffected
*Dec. Fe 
Inc.  TIBc ,transferring
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7
Q

75y +enlarged cervical LNs + several recurrent infections +place conjunctiva (anaemia 🤔) + fatigue .
Type of cells most likely in blood smear?

A
  • Mature lymphocytes
    *dx:CLL
    #Clincher:
    *Old age لوكميا العواجيز طيبة الى حد وشبه الليمفوما
    *cervical lymphadenopathy
    *recuurent infection (WBC dysfunction)
    *anaemia
    #blood
    *absolute lymphocytosis
    *AIHA
    *Dec . platelets DT BM failure
    #BM immature lymphocytes >30%
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8
Q

50y + No past medical hx + Massive splenomegly + pale conjunctivitis
FBC show :
Anemia ,massive leucocytosis ,normal platelets .
Dx?

A

*CMLchronic myeloid leukaemia
🇦🇱📢if u see massive spleen :
Think of { CML &Malaria which can be excluded with hx of travel }
🎤🏥invest:
1_FBC
* massive leucocytosis
*deferential show granulocytes at all stages
*platelet show Dec. Incr. Or N
2_inc. uric acid (Gout)
3_BM biopsy: definitive {blast &promylocytes}
4_cytogenic : pH. Chromosome .

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9
Q

14y (child_🤔) + $of pancytopenia + blood film :blast cells

Dx?

A
ALL (لوكميا الاطفال )
#blast cells in peripheral blood  سؤال 
#BM biopsy show blasts confirm the dx &amp; exclude a plastic anemia .
#ph.che. occurs in 30% &amp;associated with poor dx .
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10
Q

(28 y )+sudden onset of bone pain +( bleeding from gum) + looks pale + hepatosplenomegly + leucocytosis +blasts in peripheral blood + BM biospy show incr. Blasts .
Dx?

A

Dx:AML (emergency case)

📢leucocytosis cause bone pain

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11
Q

51y + headache (HTN)+pruritis after hot bath + DVT +incr. { RBCs,WBC,platelet} +Dec. Erythropoietin + JAK mutation screen (سؤال)
Dx?
Management?

A

PRV (polycythemia rubra vers )
incr. RBCs plethora + { hyper viscosity :MI,stroke, DVT}
incr. WBCs { basephil:pruritis }
*incr platelets: bleeding especially git .
*+
+
=splenomegly
#ttt:
1_ venesection(phlebotomy)
2_chemotherapy
(<40 ;interferon/>40y hydroxyuria )
3_Aspirin 75mg OD&raquo_space;reduce thrombotic events

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12
Q

(63y)* + thirsty + back ache + elevated Ca

Blood film most likely finding ?

A
# Rouleaux formation 
📢🎤Dx MM (multiple myeloma) 
*Age :old man 
*Bone pain {back,rib,long bone}
* pathological fr. 
*fatigue ,lethargy,
* polydepsia > polyuria dt elevat. Ca 
Pathophysio(malignant proliferation of plasma cells secreting monoclonal IG (functionless)
🚩Invest: 
*Normocytic normochromic
*ESR>100
*Electrophoresis >> monoclonal IG 
*Urine : +ve Bense jone proteins
*Plain x ray : punched out lytic lesion 
*inc. Ca
*BUN,create. Elevated 
BM diagnostic(definitive ) :plasma cell > 20% 
Blood film:rouleaux formation
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13
Q
XX presented with prolonged bleeding after dental extraction + her father &amp;paternal grandma have similar pb
What is the mood of inheritance??
Dx?
Invest to confirm?
Ttt?
A
*AD 
#dx:VWD 
🚩girl to exclude hemophilia
🏁imp. Points:
#cause mucosal bleeding eg; epistaxis ,menorrhagia
#AD 
#Role of VWF 
@promote platetet aggregation 
B) carrier molecule for factor 8 
🏴Invest;
⬆BT 
⬆APTT 
Factor 8 level ⬇
📢ttt;
1_ tranxamic acid for mild bleeding
2_desmopressin 
3_factor 8concentrate.
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14
Q

Deep Bleeding into muscle &joints

⬆PTT

A

Haemphilia (8)

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15
Q

Bleeding everywhere
⬆PTT
⬆BT
⬆PT

A

DIC

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16
Q

(Vegan)* + peripheral parasthesia + mild dyspnea + angular stomatitis + sore red tongue
Cell type on blood film ?

A

*oval macrocytic red cells
🎤📢angular stomatitis can be caused by ; b12 ⬇,FE⬇.
🎤PERIPHERAL NEURITIS dt bit b 12 ⬇

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17
Q

5y+ falling >swelling at the knee +rashes on buttock + ⬆aptt
Dx?

A
Haemophilia 
🚩mode of inheritance :x linked 
🎤males are typically affected 
🎤low level of factor 8 
Invest: 
PT ,BT,fibrinogen level &amp;VWF all normal
aPTT ⬆
Ttt: 
desmopressin
Recombinant factor 8 
Do not give IM injection .
Avoid NSAID>>give opiote
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18
Q

DVT after long flight + started on warfarin

Target INR ?

A

INR 2:3
Also this range needed for :
⬇risk of embolism for ppt with AF &valvular heart diz .
☻pt with metallic valve with lifelong anti coagulant needs INR 3:4

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19
Q

Mucosal bleeding +*petechial rashes + looks pale + ⬇RBCs,WBC,platelets
+ blood films show no retic.+BM aspiration show across reduction in all haemopoetic tissue {replaced by fat spaces}.

A
A plastic anaemia 
Pancytopenia + BM hypoplasia 
#causes : 
Autoimmune triggered by drug {[parvovirus, hepatitis}
. or radiation .
20
Q

Greek man +dark red urine + after eating fava beans+ signs of shock + blood film show spherocytes &fragments RBCs.
Dx?
Mode of inheritance?

A
Dx: G6PD ⬇
🚩spherocyes seen in : 
*hereditary spherocytosis
*AIHA
*can be seen in severe cases of hamolysis
*can be seen in G6PD ⬇
#x_linked 
#mostly affect Africa, Asia &amp; Mediterranean descent.
21
Q
#Common drug induced G6PD ⬇?
# invest. Of G6PD? 
#managements:
A

Primaquine
# invest:
*Heinz bodies in blood film of drug induced hemolysis. + GB stones also common
* ⬆retic, in. Bilirubin,⬇heptoglobin.
*blood film show spherocytes , RBCs fragments
📢📢🚩diagnostic :
G6PD ⬇
Ttt:
*Avoidance of precipitating drugs & broad fava bean .
*transfusion in severe cases.
*IV fluid

22
Q

36y Female with petecheal rash + menorrhagia ⬇platelets .

Dx?

A
Thrombocytopenia .
🚩adult ITP not commonly follow infection.
🚩📢presentation: 
Bleeding
Purpura
Epistaxis
Menorrhagia.
🎤clinically diagnosis by exclusion but definitive is BM biopsy.

📢🎤ttt:

  • bleeding
  • IV IG
  • emergency platelet transfusion in case of life threatening hge.
23
Q

4y boy + (in winter season)+ cough 🤔(URTI) arthritis + non blanching rash on legs +no hx if fever + abd .pain+ hematuria
Blood results all with normal range
Dx?
اه يا بطنى،اه يا مفاصلي ‘ايه ده البول الاحمر وايه اللى ع رجلى ده كمان

A
HSP (henoch_schonlein purpura).
#mainly clinical diagnosis
#⬆ESR ,IGA 
⬆creat. 
📢📢ttt:
Self_limiting :conservative management
NSAID for arthritis but not if renal impairment 
Corticosteroid in case of git dysfunction.
24
Q

Fatigue + constipation +on inspection : dry coarse skin ,hair loss ,cold extremities + diffuse goiter&lobulated+ peripheral smear show macrocytic anemua .

A

🚩Pernicious anaemia .
(Macroctic + autoimmune hashimoto goiter)
👅🗿all goiters grow diffuse except hashimoto (diffuse &lobulated) while goiter (diffuse & unilobuated).

25
Mild j +⬇HB +⬆retic + blood film show spherocytosis. | Most appropriate invest.?
``` #Direct coombs test. Types of autoimmune : 📢1_Warm antibody induced haemolysis ; Associated with other autoimmune like SLE Or lymphoma , CLL. c/p anaemia ,mild j ,splenomegly. Invest: Anaemia Spherocytosis in peripheral blood . ⬆retic +ve combs test 📢Cold haemagglutinin did(CHAD) : RBCs agglutinates in blood vessels in temp> 32 Causes:idiopathic,2ry to mycoplasma or EBV C/p blue discolorization in cold condition. Dx:anaemia, ⬆retic +ve coombs test . ```
26
40y +chronic smoker +HB 18 | Most useful hormone for diagnosis?
``` #erythropoietin ⬆HB +smoker=hypoxia =2ry polycythaemia. >>⬆erythropoitin 📢other forms of hypoxia in stem: High altitude CCHD chronic lung did ```
27
Septicemia + develop purpura over the legs &arms+ ⬆PT,aPTT, D_Dimer .
``` DIC C/P : *ecchymosis or spontaneous bleeding at venopuncture sites *Bleeding from orficies * petechiae,purpura. Dx: ⬆PT,PTT,D_dimar ⬇ fibrinogen, thrombocytopenia . Ttt: *treat the underling cause . Transfusion of platelets or plasma component for severe bleeding. *administer FFP . ```
28
Hx of hereditary spherocytosis + HB ⬇+ retic⬇ Most likely cause ? Mode of inheritance of HS ?
Parvovirus B19 infection . #AD 📢🚩PVB19 can cause aplastic crisis which is life threatening conditions . 🚩exclude splenic crisis where retic is high .&seen in SCA .
29
How u can confirm diagnosis of hereditary spherocytosis ? | Management
#blood film show *spherocytes & ⬆retic *MCHC ⬆ *osmotic fragility test confirm presence of spherocytes but not clarify the cause . *🚩coombs test +ve in AIHA _ve in hereditary shperocytosis . Management: 🎤steroid therapy 🎤folate supplementation 🎤splenectomy When u see parvovirus B19 think of 🤔😱SCA or HS
30
15y has marked pallor &jaundice +received regular blood transfusion +medical hx of DM + skull bossing &hepatosplenomegly Dx?
Dx: B thalassemia major . Review imp. Points : #alpha thala. Major is lethal in utero.(hydrops fetalis) #beta thala. : J +hepatosplenomegly+ frontal bossing+ marked pallor + $of iron overload 🤔📢management : *Lifelong blood transfusion to maintain HB > 9.5 *Fe chelation (oral deferiprone +desferrioxamine SC twice) + BM can be curative .
31
Epistaxis + bleeding was controlled + all blood result are normal . Dx?
Anatomical defect
32
52y + lost blood after hysterectomy + for blood transfusion | Test for preparation of blood transfusion ?
Indirect coombs test . 📢🚩direct coombs test (test pt RBCs ): used to test for autoimmune hemolytic anaemia Ex: alloimmune haemolysis Autoimmune: cold agglutinins(infectious mononucleosis) Drug induced immune mediated hemolysis : Penicillin ,cephalosporn. 📢🚩indirect coombs test(test abs in pt serum :used in prenatal testing of pregnant woman &in testing blood prior to transfusion .
33
Fatigue+ HB⬇+ ⬇MCV+;⬇ferritin | Dx?
📢Fe ⬇
34
``` Ddx of microcytic: 1_ fe ⬇: ⬇Fe, ferrtin⬇, TIBC ⬆ 2_ Thalassemia : *normal fe study * electrophoresis to see type 3_Anaemia of chronic diz *Fe ⬇ *Ferritin ⬆ * in siderblastic anaemia : the body has Fe but can't incorporate it into haemoglobin . ```
Dx of macrocytic 🚩1_ megaloblatic :hyper segmented neutrophil 🎤 b12 ⬇: *neurological pb *subacute combined degeneration of the cord ``` 🎤folic ⬇: Serum folate 🚩2_ macrocytic normoblastic : *alcohol *liver diz *hypothyroidism *Pregnancy * retic * cytotoxic drug. ```
35
Haemoltic anaemia In general show: ⬆(LDH , unconjucated bilirrubin , retic) ,⬇ heptoglobin Ddx;
``` 1_ SCA : *blood smear show sickle cells * Hb electrophoresis * treat acute>> iv fluid , morphine, o2, antibiotic . Prophylaxis >> hydroxyuria 2_ autoimmune hemolysis : coombs test +be treated with steroid . 3_ hereditary spherocytosis : Blood film show spherocytes. Osmotic fragility test Treatment :splenectomy. 4_ G6PD ⬇ Blood show >>Heinz body Check G6PD level after 6w Treated by stop caustive agent. ```
36
Recurrent spontaneous bleeding into knee joints &muscles . Factor 9 was ⬇ Dx? Ttt?
Christmas diz ( haemophilia B) Ttt: recombinant factor 9 Desmopressin has no value .
37
Confused &lethargic +;pale+ megaloblastic anaemia + in both folic acid & bit b12 Ttt for this anaemia 🤔
IM bit.b12 + start oral folic acid when B12 level become normal .
38
``` Pt on meds for ttt of RA + dizness +fatiguability+ lack of energy HB 8 MCV 106 Likely cause of anaemia ? Other causes of this type of anaemia. ```
``` Methotrexate (Folate antagonist) >macrocytic anemia. Causes of anemia : #dietary ⬇ Poor intake Excess alcohol Malabsorption( caelic diz ,IBD /jejunal resection) #meds (antifolate) Sulfasalazine, methotrexate ```
39
Fatigue &palpitations+( red sore tongue +angular stomatitis )*+koilonychia. ⬇Fe ⬇MCV Dx?
Fe ⬇anemia ()* can be caused by fe ⬇& b12⬇ Ateology: *Git hge سؤال Is the most common cause in postmenopausal &males . *menorrhagia in premenapausal *hookworm , schistomasis . *common cause of blood loss: NSAID,colon cancer, Gastric cancer, gastric &duodenal ulcer. *dietary inadequate * failure of Fe absorption *excessive requirements for Fe : pregnancy . Lab: ⬇HB, MCV,MCHC,RDW, low serum ferrtin, ⬆TIBC .
40
Smoker+!underwent a hip replacement +swollen &tender Lt leg + painful passive movement + calf tender to touch Dx?
DVT
41
Pt on warfarin therapy + advice given before hemicolectomy surgery ?
Stop warfarin &start heparin Warfarin should be stopped 5days before planned surgery. Heparin should be used instead.
42
Mild fever + feels generally tired + market loss of wt over the last 6m +(white vertically corrugated lesion on the lateral surfaces of the tongue)* dx?
Dx:HIV diz . | Hairy leukoplakia :
43
22y + SCA+dysnea+headache + lethargy + infection with parvovirus suspected Dx?
Aplastic crisis 🚩🚩🚩 Parvovirus+ SCAor hereditary spherocytosis = suspect aplastic anaemia .
44
SCA + mesentric ischemia (abd. Pain ) + avascular necrosis (femoral head) +pain
``` Thromboitic crisis of SCA . The most common type . #precipitate by cold , infection, dehydration . ```
45
SCA + sudden enlargement of the spleen +hypovolemic shock .
Sequestration crisis | If recurrent >>splenectomy .
46
SCA + $ of hemolysis
Hemolytic crisis
47
Hemolysis +thrombocytopenia | + uremia. + hx of BLOODY diarrhea
HUS