Peripheral Blood Films Flashcards

1
Q

Describe Acanthocytes

A

RBCs that show many spicules

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2
Q

What conditions result in Acanthocytes

A

Liver Disease
Hyposplenism
(Abetalipoproteinaemia)

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3
Q

Describe Basophilic RBC stippling

A

Accelerated erythropoiesis or defective Hb synthesis
Small dots (rRNA) seen at periphery of RBCs

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4
Q

What conditions result in Basophilic RBC stippling?

A

Lead poisoning
Megaloblastic anaemia
Myelodysplasia
Liver disease
Haemoglobinopathy e.g. thalassaemia

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5
Q

Describe Burr cells (echinocytes)

A

Like a sea urchin with regular spicules

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6
Q

What conditions result in Burr cells

A

Often artefact if blood has sat in EDTA prior to film being made

Uraemia
Renal failure
GI bleeding
Stomach carcinoma

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7
Q

What are Heinz bodies?

A

Inclusions on the very edge of RBCs due to denatured Hb

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8
Q

What conditions result in Heinz bodies?

A

G6PD deficiency (glucose-6-phosphate dehydrogenase)
Chronic liver disease

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9
Q

What do Howell-Jolly bodies look like?

A

Purple spots in RBCs
(Basophillic)

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10
Q

What are Howell-Jolly Bodies?

A

Nuclear remnants in RBCs

(If RBC is nucleated, purple spot will be much bigger)

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11
Q

What conditions result in Howell-Jolly bodies?

A

Post-splenectomy
Hyposplenism (e.g. sickle cell disease, coeliac disease, congenital, UC/Crohn’s, myeloproliferative disease, amyloid)
Megaloblastic anaemia
Hereditary spherocytosis

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12
Q

What does describing a peripheral blood film as Leucoerythroblastic mean?

A

There are nucleated red blood cells AND myeloid precursors in the peripheral blood

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13
Q

What conditions result in a leucoerythroblastic peripheral blood film?

A

Bone marrow infiltration i.e. myelofibrosis
Malignancy

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14
Q

Describe Pelger Huet cells

A

Hyposegmented neutrophils - 2 lobes like a dumbell

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15
Q

What are Pseudo-Pelger Huet cells?

A

Hyposegmented neutrophils that are hypogranular

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16
Q

What conditions result in Pelger Huet cells?

A

Can be congenital (lamin B receptor mutation)
or acquired
Myelogenous leukaemia

17
Q

What conditions result in pseudo-pelger huet cells?

A

Myelodysplastic syndromes

18
Q

What are polychromatic cells caused by?

A

Presence of DNA in RBCs
They are usually reticulocytes

19
Q

Describe polychromatic cells

A

Bluish red blood cells

20
Q

What conditions result in increased polychromasia?

A

Usually increased in response to a shortened RBC lifespan
e.g. Haemolytic anaemia

21
Q

What conditions result in reduced polychromasia?

A

Aplastic anaemia
Chemo

22
Q

What is right shift?

A

Increased ratio of Hypermature white cells - polysegmented polymorphs (>5 lobed nuclei)

23
Q

What causes right shift?

A

Megaloblastic anaemia
Uraemia
Liver disease

24
Q

What is left shift?

A

Increase in the ratio of immature white cells - unsegmented ‘band’ nuclei

25
What does a left shift indicate?
The reserve pool of cells is being released from the bone marrow in response to increased consumption of the circulating mature cells e.g. in infection
26
What is Rouleaux formation?
Red cells stacked on top of each other like chips in a casino
27
What causes Rouleaux formation?
Chronic inflammation Paraproteinaemia Myeloma
28
What are Schistocytes?
Fragmented parts of RBCs Typically irregularly shaped with sharp edges and no central pallor
29
What conditions result in formation of schistocytes?
Microangiopathic anaemia e.g. DIC Haemolytic uraemic syndrome Thrombotic thrombocytopenic purpura Pre-eclampsia
30
Describe spherocytes
Spherical RBCs - often a little smaller
31
What conditions result in spherocytes?
Hereditary spherocytosis Autoimmune haemolytic anaemia
32
Describe stomatocytes
RBCs where a rod or slit-like pattern replaces the central zone of pallor
33
What conditions result in stomatocytes?
Can be preparation artefact Hereditary stomatocytosis High alcohol intake Liver disease
34
Describe target cells
Bull's-eye appearance in central pallor
35
What conditions result in target cells?
Liver disease Hyposplenism Thalassaemia Iron deficiency anaemia
36
What is the common name for codocytes?
Target cells