Blood film Buzz Words Flashcards

1
Q

Acanthocytes
(Spur/spike cells)

A

RBCs show many spicules

Liver disease, hyposplenism,
abetalipoproteinaemia (rare)

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2
Q

Basophilic RBC
stippling

A

Accelerated erythropoiesis or
defective Hb synthesis, small dots
at the periphery are seen (rRNA)

Lead poisoning, megaloblastic
anaemia, myelodysplasia, liver
disease, haemoglobinopathies e.g.
thalassaemia

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3
Q

Burr cells
(Echinocyte)

A

Like a sea urchin with regular
spicules

Often an artefact if blood has sat in
EDTA prior to film being made.
Uraemia, renal failure, GI bleeding,
stomach carcinoma

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4
Q

Heinz bodies

A

Inclusions on very edge of RBCs
due to denatured Hb

Glucose-6-phosphate
dehydrogenase deficiency, chronic
liver disease

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5
Q

Howell-Jolly bodies

A

Basophilic (purple spot) nuclear
remnants in RBCs
[Note: much bigger purple spots
in nucleated RBCs)

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

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6
Q

Leucoerythroblastic

A

A phrase to denote the presence
of nucleated red blood cells and
myeloid precursors in peripheral
blood

Bone marrow infiltration i.e.
myelofibrosis, malignancy

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7
Q

Pelger Huet Cells

A

Hyposegmented neutrophil with 2
lobes like a dumbbell
Pseudo-pelger huet cells are also
hypogranular

Congenital (lamin B Receptor
mutation)
Acquired (myelogenous leukaemia
and myelodysplastic syndromes
[pseudo-pelger in MDS])

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8
Q

Polychromasia

A

Bluish red blood cells due to
presence of DNA. Polychromatic
cells are usually reticulocytes
which are immature RBCs

Usually increased naturally in
response to shortened RBC life
↑in haemolytic anaemias
↓aplastic anaemia, chemo

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9
Q

Right shift

A

Hypermature white cells -
hypersegmented polymorphs (>5
lobes to nucleus)

Megaloblastic anaemia, uraemia,
liver disease

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10
Q

Rouleaux formation

A

Red cells stacked on each other

Chronic inflammation,
paraproteinaemia, myeloma

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11
Q

Schistocytes

A

Fragmented parts of RBCs –
typically irregularly shaped with
sharp edges and no central pallor

Microangiopathic anaemia, e.g.
DIC, haemolytic uraemic syndrome,
thrombotic thrombocytopenic
purpura, pre-eclampsia

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12
Q

Spherocytes

A

Sphere shaped RBCs
Often a little smaller

Hereditary spherocytosis,
Autoimmune Haemolytic Anaemia

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13
Q

Stomatocytes

A

Central pallor is straight, curved
or rod-like shape. RBCs appear
as ‘smiling faces’ or ‘fish mouth’

Can be an artefact during slide
preparation.
If not: Hereditary stomatocytosis,
high alcohol intake, liver disease

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14
Q

Target cells
(codocyte)

A

Bull’s-eye appearance in central
pallor

Liver disease, hyposplenism,
thalassaemia, IDA

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