diagnosis & further tests Flashcards

1
Q

What to expect w/ condition of ovalocytes, *(include more0

A
  • Macrocytic
  • ovalocyte
  • hypersegmentation*
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2
Q
Dx this? & what further testing would you do?
FBC
- dec. Hb
- variable MCV
- sub.-pop of RBC

Peripheral blood film

  • poikilocytosis: spherocytes*, schistocytes
  • polychromasia (+++)
  • nRBC
  • inc reticulocytes (>2%)
A

Dx: Haemolytic anaemia

  • dec. Hb = anaemia
  • variable MCV = macrocytes /reticulocytes
  • polychromasia = reticulocytes
  • reticulocytes = inc erythropoeisis = compensate for anaemia

Further tests

  • Osmotic fragility = inc bc if mostly macrocytic
  • Serum bilirubin bc low Hb = inc bilirubin released
  • Direct antiglobulin test (DAT) > see if haemolysis is due to Ab
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3
Q

Dx this?

  • Spherocytes
  • osmotic fragility inc
  • DAT: negative
  • Reticulocytosis
A

Hereditary spherocytosis

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4
Q

Dx this?
>25% eliptocytes
~4% reticulocytes

A

hereditary elliptocytosis

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5
Q

Dx this? & further tests

  • +++ stomatocytes
  • macrocytosis
A

Dx: hereditary stomatocytes

Further test

  • positive osmotic fragility test
  • ektacytometric analysis
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6
Q

Dx this? & further test

- BF: heinz bodies, Bliseter cells, Bite cells, hemighost cells, shistocytes

A

-Dx: glucose-6-phosphate dehydrogenase deficiency
Further test
- Fluorescent screen test = dec. NADPH, dec. fluorescence
- Definitive test = G6PD enzyme assay

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7
Q

Dx this?

  • echinocytes
  • reticulocytosis
A

pyruvate kinase deficiency

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8
Q

Dx this? & further test?

  • FBC: macrocytosis (MCV), reticulocytosis
  • BF: aggregates of RBC, Poikilocytosis, inc polychromasia
A

Dx: AIHA cold type

  • Test: DAT
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9
Q
  • anemia,
  • normocytic, normochromic,
  • inc RDW (anisocytosis),
  • reticulocytosis,
  • hyperchromic/spheroc.
  • BF: SPHEROCYTES*, inc. polychromasia/reticulo.
A
Dx: AIHA warm type
Further test:
- test: DAT = positive (IgG)
 - osmotic fragility = inc., 
- Ind. bilirubin = inc
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10
Q

Dx this?
- AIHA
+ immune thrombocytopenia
+/or netropenia

A

evan’s syndrome

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11
Q

What’s the condition that has

  • Thrombocytopenia
  • Anaemia
  • leukopenia
A

pancytopenia

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12
Q

Leokocytosis further testing

A
  • immunophenotype

- Functional assay

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13
Q

Dx reactive lymphocytosis

A
  • **Viral infections
  • Bacterial Infections
  • Other infections: malaria
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14
Q

Dx (at chronic phases) & further tests*

  • leukocytosis (+ or +++ inc in WBC)
  • Inc granulocyte?*
  • Eosinophilia, basophilia
  • ~50 mature neutrophils
  • (>10% blast = accelerated phase)
A

Dx: Chronic myeloid leukaemia

Further tests:*

  • cytogenetics to detect translocation in 9, 22
  • FISH (fluorescence in situ hybridisation) to confirm fusion of genes
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15
Q

Dx this? & Fyrther test?*

  • inc Hb, PCV & RBC (*not always Hi)
  • Thrombocytosis
  • Granulocytosis
A

Dx: Polycythaemia vera

Further test*

  • Epo conc. ?*
  • JAK2?*
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16
Q

Dx this? & Further test?

  • Thrombocytosis
  • anisocytosis of plts (sml to giant)
  • microcytic, hypochromic anaemia
A

Dx: Essential thrombocythaemia

Further test:
- JAK?*

17
Q

Dx this? Further test?

  • Left shift granulocytes
  • Atypical MK
  • Some (+, ++) microcytoc hypochromic anaema
A

Dx: Primary myelofibrosis - fibrotic phase

18
Q

Dx this? Further test?

  • monocytosis
  • Leukocytosis (inc WBC)
  • normal morphology (<20% blast)
A

Dx: Chronic myelomonocytic leukaemia (CMML)

Further test:

  • Cytogenetics = neg
  • BM assessment
19
Q

Reasons/situations to explain reactive lymphocytes in cytoplasm

A
  • Viral infections: influenza
  • bacterial infections: tuberculosis
  • Other infections: malaria
  • Non-infectious: e.g. hypersensitivity
20
Q

Dx this? Further test?

  • Inc MCV
  • Normochromic
  • Ovalocytes
  • mild to marked anaemia
A

Dx: Megaloblastic macrocytic anaemia
Further test:
- FOlate test: bc could be deficient in folic acid
- Vit. B12 test bc could be defiecient

21
Q

Dx this? and further treatment

  • anaemia
  • leukopenia
  • thrombocytopenia
  • > 20% blast celles
A

Dx: acute leukaemia

Further test:

  • Immunophenotype (detect cell linage affected?)
  • Cytogenetic & genetic analysis
22
Q

diagnosis basophilic stippling (granules) in RBC

A

D: sideroblastic anaemia (granules of iron in RBC)
FT: iron studies like ferritin test

23
Q

dx this? further testing

  • smudge cells
  • lymphocytosis
  • neutropenia, thrombocytopenia
A

Dx: (chronic) lymphocytic leukaemia
Further testing:
- immunophenotype

further test:
- immunophenotype: CD5+

24
Q

dx this?

  • MICROCYTIC
  • HYPOCHROMIC
  • DACROCYTES/poikilocytes
  • occasional HbH includions
A

dx: (alpha) thalassemia (minor)
further testing:
Hb electrophorhesis: HPLC (can distinguish to IDA -> abnormal iron studies results)

25
dx this? further test - microcytosis - dacrocytes - intracell. crystal - inc MCHC
dx: HbC disease FT: Hb Id
26
Dx this? F tests - from lymphopenia to -cytosis - neutropenia, thrombocytopenia - fine cytoplasmic projections like hair - AIHA
dx: hairy cell leukaemia further test: - CD19+ - cytohem: pos for TRAP - **molecular studies: BRAF V600E*
27
what is satellitosis?
artefact: plts stuck on periphery of neutrophil | bc interacting w/ EDTA
28
further testing if detect malaria (Plasmodium) in RBC
- confirm sp. by molecular testing
29
dx this & FT - intracellular bacteria in WBC - vacoulation in neutrophil
dx: bacteremia | FT: blood culture
30
what could rouleaux indicate
inflammatory disorder
31
dx this? & FT - low MCV - microcytes ++ - (inc RCC)
dx; iron deficient erythropoeisis FT: iron testing
32
dx this | - marked nRBC
dx: normoblastemia
33
dx this & further test - thrombocytopenia - SCHISTOCYTES
dx: DIC FT: PT - antithrombin levels - coagulation test