Derivation: mixed language: base [cationic] philien [to love] stippen [to prick]
The inclusions are blue, fairly evenly spread throughout the erythrocyte cytoplasm and generally too frequent to easily count (typically there will be considerably more than 10 dots present). When fine it may be difficult to detect at low power, and may be best detected by gently focussing up and down at high power. Coarse stippling may also be seen, and this is more easily detected.
Image 1 Many fine blue dots are distributed fairly evenly throughout the erythrocyte cytoplasm. In contrast to other dot like inclusions the dots are very frequent (too many to count). This image shows relatively fine stippling, note that the appearance can be more coarse (see clinical images). An underlying cause shopuld be sought, for example - hypochromia and microcytosis (thalassaemia) or misshapen erythrocytes and dysplastic white cells (MDS).
Basophilic stippling most commonly arises when blood cell production is stressed or abnormal, so it is important to look at clinical features and other morphology for clues (see causes). Although rare, it is important to realise that basophilic stippling may be associated with dysfunction of enzymes involved in RNA breakdown (either congenital deficiency or drug induced) (see Pathobiology).
Basophilic stippling will rarely be confused with other inclusions due to their large number, and diffuse distribution. Occasionally Pappenheimer bodies (which can be multiple) can be confused, but Pappenheimer bodies are usually much fewer in number, tend not to have a uniform distribution, and typically have a grey/blue rather than pure blue colour. It is generally useful to distinguish fine (often reactive) from coarse (more frequently pathological) stippling.
Clinical Image 1 A teardrop poikilocyte with prominent stippling, note the even distribution of many fine basophilic inclusions. Note also the large platelet and range of abnormal red cell forms. Clinical disorder: myelofibrosis.
Clinical Image 2 Fine basophilic stippling within a polychromatic erythrocyte. Note the many abnormal red cell forms in the background including irregularly contracted erythrocytes and one target cell; as well as absent platelets. Clinical disorder: myelodysplasia.
Clinical Image 3 A further example of fine basophilic stippling within a polychromatic erythrocyte. Note that in this case the remaining erythrocytes are predominantly hypochromic and platelets are plentiful. Clinical disorder: thalassaemia.
Ribosomes are the cellular organelles that produce haemoglobin in developing red cells. Ribosomes take up blue dyes, and therefore give the characteristic blue colour to immature erythrocytes or reticulocytes; when no longer required the ribosomes are removed by the spleen so mature red cells do not have any blue shading. Where red cell production is abnormal or stressed the ribosomes are retained in mature erythrocytes; these then form aggregates during the staining process causing these typical blue dots. A more specific cause is deficiency of the enzyme pyrimidine 5’nucleotidase – the absence of this enzyme impairs RNA breakdown causing ribosomes to be retained in mature cells. Lead or other heavy metal poisoning can also inhibit this enzyme causing stippling.