Pancytopenia Flashcards

1
Q

Describe what is meant by pancytopaenia

A

Pancytopaenia refers to a decrease in all peripheral blood cell lines.:
- red blood cells (RBCs)
- white blood cells (WBCs)
- platelets.

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2
Q

What exact values determine that pancytopaenia is present [3]

A

Haemoglobin:
- < 115 g/L (women), < 130 g/L (men)

Leucocytes:
- < 4.0 x109/L
OR

Neutrophils:
- < 1.5 x 109/L

Platelets:
- < 150 x109/L

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3
Q

Pancytopaenia may be caused by which three broad mechanisms? [3]

A

Bone marrow suppression:
- the process of haematopoiesis is reduced preventing blood cell production.

Bone marrow infiltration:
- the bone marrow is infiltrated (e.g. malignant cells, microorganisms) impairing its ability to conduct haematopoiesis.

Blood cell destruction:
- there is an increased turnover of blood cells in the peripheral circulation due to destruction or sequestration in organs (e.g. spleen).

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4
Q

Name causes for the different categories of pancytopaenia:

Haemotological [4]
Metatstatic [3]
Infections [4]

A

Haemotological:
- Leukaemia
- Lymphoma
- Multiple myeloma
- Myelodysplastic syndromes

Metatstatic:
- Lung cancer
- Breast cancer
- Prostate carcinoma

Infections
- TB
- Fungal
- HiV
- Parvovirus B19

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5
Q

Name causes for the different categories of pancytopaenia:

Nutrional deficiencies [3]
Medications and toxins [4]
Autoimmune disorders [3]

A

Nutrional deficiencies:
- Vitamin B12
- Folate
- Anorexia nervosa

Medications and toxins:
- Alcohol
- chemotherapy
- azathioprine
- methotrexate,
- carbamazepine

Autoimmune disorders:
- aplastic anaemia
- rheumatoid
- SLE

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6
Q

Name causes for the different categories of pancytopaenia:

Peripheral destruction [1]
Peripheral sequestration [1]
Congenital [2]

A

Peripheral destruction
- Disseminated intravascular coagulation

Peripheral sequestration
- portal hypertension

Congenital:
- Wiskott Aldrich syndrome,
- Fanconi anemia

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7
Q

What are the common characteristic features of pancytopaenia? [3]

A

Lethargy (anaemia)
Weakness (anaemia)
Pallor
Bruising (low platetlets)
Bleeding
Recurrent infections (leucopaenia)

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8
Q

What examination findings should you look for in a patient with suspected pancytopaenia? [7]

A
  • Lymphadenopathy
  • Organomegaly (e.g. splenomegaly, hepatomegaly)
  • Scleral findings: pale, jaundiced
  • Oral findings: ulcers, thrush (e.g. as immunocompromised)
  • Features of cardiac failure (e.g tachypnoea, raised JVP, crackles on auscultation, peripheral oedema): due to symptomatic anaemia
  • Skin findings: pale, jaundiced, bruising, petechiae, purpura
  • Other: joint pain or swelling, sarcopenia, active bleeding
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9
Q

What peripheral blood film results would indicate pancytopaenia? [6]

Which pathologies would these indicate? [6]

A

Circulating blasts (i.e. immature white blood cells): suggestive of leukaemia

Abnormal / dysplastic white cells: suggestive of myelodysplastic syndrome

Immature white blood cells: suggestive of myeloproliferative disorder

Hypersegmented neutrophils: suggestive of megaloblastic anaemia (e.g. B12 deficiency)

Schistocytes (fragmented red blood cells): suggestive of peripheral destruction

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10
Q

What follow up testing would you investigate with after a peripheral blood film for suspected pancytopaenia? [4]

A
  • bone marrow aspirate
  • biopsy
  • flow cytometry
  • cytogenetic testing
  • molecular studies.

A bone marrow biopsy is particularly important in patients with a suspected primary haematological disorder.

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11
Q

Which further specialist tests would you use to investigate pancytopaenia? [5]

A
  • Autoimmune / vasculitis screen
  • Malaria screen
  • Viral screen (e.g. HIV, hepatitis B/C)
  • Serological tests for infections
  • Bone marrow biopsy
  • Lymph node biopsy
  • CT-PET
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12
Q
A
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