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Clinical approach to
anemia:
Case scenarios
Dr/ Marwa Mahmoud Khalifa
MD PHD Internal Medicine & Hematology
Case 1
• 35 y old female came to clinic complaining of
fatigue , dizziness.
• She was pale, with history of menorrhagia related
to the use of IUD.
• CBC: HB 6.5 , MCV 56, MCH 19,
Normal PLT, WBC
Cont. Case 1
•Next step?
• Urgent packed RBCs transfusion
• Parenteral iron therapy
• Oral iron therapy
• Other
Cont. Case 1
• Iron profile was requested
• Ferritin
• Iron
• TIBC
Case 2
• 70 year old male presented with anemia (iron
deficiency) , recurrent abdominal pain
• His treating physician prescribed oral iron and
antispasmodics with diagnosis of IBS
• Hb increased from 7 to 9 gm/dl then declined to 8
gm/ dl
• His doctor asked for occult blood in stool 
negative so he recommended parenteral iron.
Cont. Case 2
• Hb level reached 10 gm/dl then started to decline
to 8.5 and the patient was referred to the
hematologist.
• What’s the next step??
Cont. Case 2
• Repeat fecal occult blood
• Repeat iron profile
• Packed RBCs transfusion
• Upper & lower GI endoscopy
• CT enterocolonography
Case 3
• 27 year old female patient presented with pallor ,
fatigue
• She did Hb level was 8.5 gm/dl and started to
take oral iron supplement
• One month later, Hb was the same
• So she sought medical advice
Cont. Case 3
• CBC:
• Hb 8 gm/dl
• RBCs 4.7 x106 /mm
• MCV 56 fl
• MCH 19 pg
• RDW 15
• Ferritin 144
Cont. Case 3
• Hb electrophoresis
Case 4
• 16 year old male patient , known to have G6PD
deficiency
• CBC was done as a routine check up
• Hb 12 gm/dl
• RBCs 6.14 x106 /mm
• MCV 68 fl
• MCH 19.7 pg
Cont. Case 4
• Ferritin 155 ng/ml
• Iron 53 mcg/dl
• TIBC 256 mcg/dl
• Transferrin saturation 20%
• Hb electrophoresis normal
(HbA 96.77%, HbA2 3.23%)
Cont. Case 4
• Alfa , beta thalassemia gene mutation were requested
Case 5
• 10 year old child , his father has sickle cell
disease, his mother noticed that he is pale.
• CBC
Hb 9.5 gm/dl
RBCs 3.5 x106 /mm
MCV 72 fl
MCH 23 pg
• Ferritin 8 ng/ml
Cont. Case 5
Case 6
• 50 year old female patients presents with bone
pains
• A rheumatologist asked for the following
CBC : Hb 10 gm/ dl normocytic
ESR : more than 100
RF , anti CCP : negative
Sero negative RA  MTX for 3 months
Cont. Case 6
• Follow up pain not relieved, Hb 8 gm/dl, ESR
still >100
• Referred to heamatologist for correcting anemia
Cont. Case 6
CBC film : normocytic anemia , rouleux formation
RFT: creatinine 1.89 mg/dl , uric acid 8.5 mg/dl
Ca : 12 mg/dl
SPEP: M band
SIF: IgG kappa
Case 7
• 65 year old female patient presented with pallor,
easy fatigue
• Past history : hypertension 3 months ago, OA,
habitual constipation
• CBC : Hb 9.5gm/dl, MCV 100, MCH normal,
normal PLT, WBC
• Next step?
Cont. Case 7
• Thyroid profile was requested
TSH 18
FT4 0.15
L-troxin was initiated
• 8 weeks later
Thyroid profile : normalized
Hb 12 gm/dl
Case 8
• 38 year old male patient presented with anemia
• No other symptoms
• CBC was done :
Hb 8.2 g/dl , MCV 91, MCH 29
PLT 75
WBC 4.6 with normal differential
• What’s the next step?
Cont. Case 8
• ESR was normal
• Virology (HBsAg, HCV Ab, HIV Ab) : negative
• ANA, Anti dsDNA: negative
• US abdomen: no organomegaly
Cont. Case 8
• BMA &biopsy were requested :
Hemodiluted aspirate, biopsy was hypocellular for
age and diminshed hematopoeitic precursors
Aplastic Anemia
Case 9
• 39 year old female patient , with history of
bypass bariatric surgery 18 months ago,
presented with pallor and tingling sensation
allover her body.
• CBC: Hb 8.5g/dl, MCV 98cmm, MCH 22 pg,
PLT 110, WBC 3.2
• CBC film: Dimorphic RBCs, hyposegmented
neutrophils
Cont. Case 8
• S ferritin
• S B12
Case 9
• 23 year old female patient presented with acute
onset of anemia , jaudice
• CBC: Hb 7g/dl, MCV110, MCH 28, PLT normal ,
WBC normal
• Bilirubin Total 5.7mg/dl, indirect 4.8mg/dl, direct
0.9mg/dl
Cont. Case 9
• Reticulocyte 8%
• LDH 596
• ESR 110
• Virology negative
• US abdomen normal
Cont. Case 9
• Cross matching can’t be done
• Coomb’s test ( direct & indirect): positive
AIHA
Cont. Case 9
• ANA : 1/320
• Anti dsDNA: 150
SLE with secondary AIHA
Case 10
• 58 year old male patient no past medical history
presented with clinical manifestations of anemia,
jaundice
• No palapable lymphadenopathy/ organomegaly
• CBC : Hb 7.5g/dl, MCV 108, PLT 280, WBC
28.000 of which 90% mature lymphocytes
• Bilirubin Total 4.6 , indirect 3.6
Cont. Case 10
• Retic: elevated
• LDH: elevated
• Coomb’s test (direct, indirect): positive
• Immunophenotyping chronic pannel :CLL
CLL with secondary AIHA
Case 11
• 52 years old male patient known to have thalassemia trait
with a baseline Hb 10g/dl presented with sudden fall Hb
to 4g/dl , deep jaundice bilirubin 6.5mg/dl mainly
indirect.
• PLT 27, WBC 6.000 with normal differential
• What’s the next step?
Cont. Case 11
• Retic :
• Coomb’s test : positive
• US abdomen : mild splenomegaly 13 cm
• Virology: negative
• BMA & biopsy: no infiltration, increased erythropoeisis
and megakaryocytes
Evan’s Syndrome
Case 12
• 27 year old male patient complained with easy
fatigue, dizziness, recurrent abdominal pain
mainly Lt hypochondrium relieved by analgesics
and antispasmodics.
• On examination splenomegaly (5 fingers below
costal margin)
Cont. Case 12
• CBC :
Hb 8 g/dl, MCV 87, MCH 27, PLT 358, WBC 296
Differential : absolute neutrophilia, absolute
basophilia, absolute monocytosis, myelocytes,
metamyelocytes, blasts 6%
Cont. Case 12
• QPCR BCR-ABL210 : positive
CML
Case 13
• 60 year old female patient presented with fatigue,
exertional dyspnea, anemia, one attack of
epistaxis and recurrent abdominal pain
• PMH : uterine prolapse
• Admitted to Damanhour fever hospital
• CBC Hb 5g/dl MCV 70, MCH 20, PLT 158,
WBC25.000 with absolute lymphocytosis
Cont. Case 13
• US abdomen :liver cirrhosis, portal vein not
dilated, huge splenomegaly~25cm
• Normal renal and liver functions
• HBsAg negative, HCV Ab positive, HCV RNA
positive
• Upper GI endoscopy : antral gastritis only !!!
Cont. Case 13
• Anemia ?
• Cause of bleeding ?
• Splenomegaly?
• Lymphocytosis?
Cont. Case 13
• CBC film :rouleux formation
• SPEP : M band
• Ig M : markedly elevated
• Flowcytomery peripheral blood + BMB :
Lymphoplasmacytic lymphoma
Case 14
• 38 year old female patient presented with alleged
convulsions, no prior history, went to ER in
general hospital and diagnosed as being
hysterical and discharged
• In the following day, she had a syncopal attack,
so she went to a private clinic.
Cont. Case 14
• She was pale, ecchymotic patches on body side ,
vitally stable except for being febrile (37.9)
without any obvious source of infection
• DD??
Cont. Case 14
• CBC with film : Hb7 g/dl, PLT 10, WBC 13.000
neutropilia with toxic granulations, schistocytes
TTP
clinical.pptx

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clinical.pptx

  • 1. Clinical approach to anemia: Case scenarios Dr/ Marwa Mahmoud Khalifa MD PHD Internal Medicine & Hematology
  • 2.
  • 3.
  • 4. Case 1 • 35 y old female came to clinic complaining of fatigue , dizziness. • She was pale, with history of menorrhagia related to the use of IUD. • CBC: HB 6.5 , MCV 56, MCH 19, Normal PLT, WBC
  • 5. Cont. Case 1 •Next step? • Urgent packed RBCs transfusion • Parenteral iron therapy • Oral iron therapy • Other
  • 6. Cont. Case 1 • Iron profile was requested • Ferritin • Iron • TIBC
  • 7. Case 2 • 70 year old male presented with anemia (iron deficiency) , recurrent abdominal pain • His treating physician prescribed oral iron and antispasmodics with diagnosis of IBS • Hb increased from 7 to 9 gm/dl then declined to 8 gm/ dl • His doctor asked for occult blood in stool  negative so he recommended parenteral iron.
  • 8. Cont. Case 2 • Hb level reached 10 gm/dl then started to decline to 8.5 and the patient was referred to the hematologist. • What’s the next step??
  • 9. Cont. Case 2 • Repeat fecal occult blood • Repeat iron profile • Packed RBCs transfusion • Upper & lower GI endoscopy • CT enterocolonography
  • 10.
  • 11. Case 3 • 27 year old female patient presented with pallor , fatigue • She did Hb level was 8.5 gm/dl and started to take oral iron supplement • One month later, Hb was the same • So she sought medical advice
  • 12. Cont. Case 3 • CBC: • Hb 8 gm/dl • RBCs 4.7 x106 /mm • MCV 56 fl • MCH 19 pg • RDW 15 • Ferritin 144
  • 13. Cont. Case 3 • Hb electrophoresis
  • 14. Case 4 • 16 year old male patient , known to have G6PD deficiency • CBC was done as a routine check up • Hb 12 gm/dl • RBCs 6.14 x106 /mm • MCV 68 fl • MCH 19.7 pg
  • 15. Cont. Case 4 • Ferritin 155 ng/ml • Iron 53 mcg/dl • TIBC 256 mcg/dl • Transferrin saturation 20% • Hb electrophoresis normal (HbA 96.77%, HbA2 3.23%)
  • 16. Cont. Case 4 • Alfa , beta thalassemia gene mutation were requested
  • 17. Case 5 • 10 year old child , his father has sickle cell disease, his mother noticed that he is pale. • CBC Hb 9.5 gm/dl RBCs 3.5 x106 /mm MCV 72 fl MCH 23 pg • Ferritin 8 ng/ml
  • 19. Case 6 • 50 year old female patients presents with bone pains • A rheumatologist asked for the following CBC : Hb 10 gm/ dl normocytic ESR : more than 100 RF , anti CCP : negative Sero negative RA  MTX for 3 months
  • 20. Cont. Case 6 • Follow up pain not relieved, Hb 8 gm/dl, ESR still >100 • Referred to heamatologist for correcting anemia
  • 21. Cont. Case 6 CBC film : normocytic anemia , rouleux formation RFT: creatinine 1.89 mg/dl , uric acid 8.5 mg/dl Ca : 12 mg/dl SPEP: M band SIF: IgG kappa
  • 22. Case 7 • 65 year old female patient presented with pallor, easy fatigue • Past history : hypertension 3 months ago, OA, habitual constipation • CBC : Hb 9.5gm/dl, MCV 100, MCH normal, normal PLT, WBC • Next step?
  • 23. Cont. Case 7 • Thyroid profile was requested TSH 18 FT4 0.15 L-troxin was initiated • 8 weeks later Thyroid profile : normalized Hb 12 gm/dl
  • 24. Case 8 • 38 year old male patient presented with anemia • No other symptoms • CBC was done : Hb 8.2 g/dl , MCV 91, MCH 29 PLT 75 WBC 4.6 with normal differential • What’s the next step?
  • 25. Cont. Case 8 • ESR was normal • Virology (HBsAg, HCV Ab, HIV Ab) : negative • ANA, Anti dsDNA: negative • US abdomen: no organomegaly
  • 26. Cont. Case 8 • BMA &biopsy were requested : Hemodiluted aspirate, biopsy was hypocellular for age and diminshed hematopoeitic precursors Aplastic Anemia
  • 27. Case 9 • 39 year old female patient , with history of bypass bariatric surgery 18 months ago, presented with pallor and tingling sensation allover her body. • CBC: Hb 8.5g/dl, MCV 98cmm, MCH 22 pg, PLT 110, WBC 3.2 • CBC film: Dimorphic RBCs, hyposegmented neutrophils
  • 28. Cont. Case 8 • S ferritin • S B12
  • 29. Case 9 • 23 year old female patient presented with acute onset of anemia , jaudice • CBC: Hb 7g/dl, MCV110, MCH 28, PLT normal , WBC normal • Bilirubin Total 5.7mg/dl, indirect 4.8mg/dl, direct 0.9mg/dl
  • 30. Cont. Case 9 • Reticulocyte 8% • LDH 596 • ESR 110 • Virology negative • US abdomen normal
  • 31. Cont. Case 9 • Cross matching can’t be done • Coomb’s test ( direct & indirect): positive AIHA
  • 32. Cont. Case 9 • ANA : 1/320 • Anti dsDNA: 150 SLE with secondary AIHA
  • 33. Case 10 • 58 year old male patient no past medical history presented with clinical manifestations of anemia, jaundice • No palapable lymphadenopathy/ organomegaly • CBC : Hb 7.5g/dl, MCV 108, PLT 280, WBC 28.000 of which 90% mature lymphocytes • Bilirubin Total 4.6 , indirect 3.6
  • 34. Cont. Case 10 • Retic: elevated • LDH: elevated • Coomb’s test (direct, indirect): positive • Immunophenotyping chronic pannel :CLL CLL with secondary AIHA
  • 35. Case 11 • 52 years old male patient known to have thalassemia trait with a baseline Hb 10g/dl presented with sudden fall Hb to 4g/dl , deep jaundice bilirubin 6.5mg/dl mainly indirect. • PLT 27, WBC 6.000 with normal differential • What’s the next step?
  • 36. Cont. Case 11 • Retic : • Coomb’s test : positive • US abdomen : mild splenomegaly 13 cm • Virology: negative • BMA & biopsy: no infiltration, increased erythropoeisis and megakaryocytes Evan’s Syndrome
  • 37. Case 12 • 27 year old male patient complained with easy fatigue, dizziness, recurrent abdominal pain mainly Lt hypochondrium relieved by analgesics and antispasmodics. • On examination splenomegaly (5 fingers below costal margin)
  • 38. Cont. Case 12 • CBC : Hb 8 g/dl, MCV 87, MCH 27, PLT 358, WBC 296 Differential : absolute neutrophilia, absolute basophilia, absolute monocytosis, myelocytes, metamyelocytes, blasts 6%
  • 39. Cont. Case 12 • QPCR BCR-ABL210 : positive CML
  • 40. Case 13 • 60 year old female patient presented with fatigue, exertional dyspnea, anemia, one attack of epistaxis and recurrent abdominal pain • PMH : uterine prolapse • Admitted to Damanhour fever hospital • CBC Hb 5g/dl MCV 70, MCH 20, PLT 158, WBC25.000 with absolute lymphocytosis
  • 41. Cont. Case 13 • US abdomen :liver cirrhosis, portal vein not dilated, huge splenomegaly~25cm • Normal renal and liver functions • HBsAg negative, HCV Ab positive, HCV RNA positive • Upper GI endoscopy : antral gastritis only !!!
  • 42. Cont. Case 13 • Anemia ? • Cause of bleeding ? • Splenomegaly? • Lymphocytosis?
  • 43. Cont. Case 13 • CBC film :rouleux formation • SPEP : M band • Ig M : markedly elevated • Flowcytomery peripheral blood + BMB : Lymphoplasmacytic lymphoma
  • 44. Case 14 • 38 year old female patient presented with alleged convulsions, no prior history, went to ER in general hospital and diagnosed as being hysterical and discharged • In the following day, she had a syncopal attack, so she went to a private clinic.
  • 45. Cont. Case 14 • She was pale, ecchymotic patches on body side , vitally stable except for being febrile (37.9) without any obvious source of infection • DD??
  • 46. Cont. Case 14 • CBC with film : Hb7 g/dl, PLT 10, WBC 13.000 neutropilia with toxic granulations, schistocytes TTP