Pancytopenia Flashcards

1
Q

What is pancytopenia?

A

Decrease in the number of RBC’s, WBC’s and platelets in the peripheral blood flow

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2
Q

What are the different causes for pancytopenia?

A

“Decreased production of blood cells (bone marrow failure, or immune-mediated destruction of blood cells) or non-immune-mediated sequestration in the periphery/spleen. ”-RBCs trapped in spleen:
1. Congenital causes:
- Gaucher’s disease (marrow infiltration, splenomegaly)
- Fanconi’s anaemia (bone marrow failure)
2. Acquired (decreased bone marrow production):
- Cytotoxic chemotherapy
- radiotherapy
- Megaloblastic anaemia
- Bone marrow infiltration
- Myelodysplasia
- Myelofibrosis
- Idiopathic aplastic anaemia
3. Increased/ decreased sequestration:
- liver disease
- Portal hypertension

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3
Q

What are the risk factors for pancytopenia?

A
  1. Aplastic Anaemia → type of anaemia caused by bone marrow failure
    - Normochromic, normocytic anaemia
    - Leads to decrease of all cells (pancytopenia) ⇒ ie. leukopenia, anaemia, thrombocytopaenia
  2. Acute & Chronic Leukaemia
  3. Myelofibrosis
  4. Multiple Myeloma → malignancy characterised by plasma cell proliferation
  5. Methotrexate → can lead to bone marrow suppression
  6. Chemotherapy + Radiotherapy
  7. B12 or Folate Deficiency
  8. Lymphoma
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4
Q

What are the presenting symptoms of pancytopenia?

A

Symptoms of anaemia/leukopenia/thrombocytopenia → SOB, pale skin, fatigue, weakness, fever, easy bruising, petechiae, purpura, bleeding gums and nosebleeds, recurrent infections 

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5
Q

What signs of pancytopenia can be found on physical examination?

A
  1. sign:
    - Leukaemic infiltrates (acute leukaemia) 
    - Jaundiced sclera
    - Tachycardia, oedema, congestive cardiac failure
    - Clubbing (lung cancer) 
    - Tachypnoea (sign of symptomatic anaemia) 
    - Right upper quadrant tenderness (hepatitis) 
    - Lymphadenopathy (infection, lymphoproliferative disorder, HIV disease) 
    - Signs of chronic liver disease 
    - Splenomegaly (infection, myeloproliferative and lymphoproliferative disorders) 
  2. Skin examination 
    - Malar rash (SLE) 
    - Purpura/bruising (thrombocytopenia) 

 3. Signs associated with HIV disease 
- Morbilliform rash early 
- Kaposi’s sarcoma, ulcerating nodules later 

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6
Q

What investigations are used to diagnose/ monitor pancytopenia?

A
  1. FBC and Blood Smear
  2. Bone Marrow Aspiration + Biopsy → see if issue is with bone marrow
    - Look for underlying cause
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7
Q

How is pancytopenia managed?

A
  • RBC and Platelet Transfusion
  • Bone Marrow/Stem Cell Transplant
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8
Q

What complications may arise following pancytopenia?

A
  • excess bleeding if platelets are affected 
  • increased risk for infections if white blood cells are affected 
  • Severe pancytopenia can be life-threatening. 
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