Actions

Keratocytes: Difference between revisions

From haematologyetc.co.uk

No edit summary
No edit summary
 
(15 intermediate revisions by the same user not shown)
Line 11: Line 11:


<gallery mode="nolines" widths="240px" heights="240px" border="1px" >
<gallery mode="nolines" widths="240px" heights="240px" border="1px" >
File:Kt1.png|link={{filepath:Kt1.png}}
File:Kt1A.png|link={{filepath:Kt1A.png}}
File:Kt2.jpg|link={{filepath:Kt2.jpg}}
File:Kt2.jpg|link={{filepath:Kt2.jpg}}
</gallery>
</gallery>
Line 17: Line 17:


<span style="font-style:italic; font-size:100%;'' >
<span style="font-style:italic; font-size:100%;'' >
'''Images:''' Note the two typical horns surrounding a central depression in the drawn image - the origin as a vacuole that has ruptured (see Pathogenesis) is easy to imagine. The clinical image shows one typical keratocyte (upper cell), but also emphasises the more widespread damage that may accompany these forms.
'''Images:''' Note the two typical horns surrounding a central depression in the drawn image - the origin as a vacuole that has ruptured (see Pathogenesis) is easy to imagine. The cartoon image shows one typical keratocyte (arrowed), but also emphasises the more widespread damage that ofetn accompany these forms with other damaged cells and precursor red cells present.
</span>
</span>


Line 23: Line 23:




Significance
'''Significance'''


The presence of keratocytes always implies the mechanical destruction of erythrocytes and is therefore highly significant and often requires urgent reporting. In some (although not all) cases, the pathological process may be life threatening particularly if they are associated with disseminated intravascular coagulation (DIC) or thrombotic thrombocytopenic purpura (TTP) knowledge of platelet count, clotting and additional morphological features such as fragments is essential.
The presence of keratocytes always implies the mechanical destruction of erythrocytes and is therefore highly significant and often requires urgent reporting. In some (although not all) cases, the pathological process may be life threatening particularly if they are associated with disseminated intravascular coagulation (DIC) or thrombotic thrombocytopenic purpura (TTP) knowledge of platelet count, clotting and additional morphological features such as fragments is essential.


'''Pitfalls'''


Pathobiology
The keratocyte istself is quite distinctive, however be aware of the range of causes that are not limited to microvascular damage. The appearance may also be a sign of ocidative damage or Heinz body removal. Careful attention to other features is important.
The horn-like paired projections are caused by trauma to the cell; this is most commonly caused by slicing of the cell by fibrin strands within the microvasculature. The damage is followed by repair through spontaneous membrane fusion forming a pseudovacuole; this fragile structure rapidly ruptures giving rise to the characteristic appearance of a concave defect, with surrounding horns that are the residual walls of the vacuole.
Pitfalls The appearance of the keratocyte is characteristic. However, there are two potential sources of confusion: first when multiple horns are present on the cell, where they need to be distinguished from echinocytes or acanthocytes: look for the characteristic depression between the horns. When damage is more severe the keratocytes become increasingly irregular, form small sharp-edged fragments which can usually be detected. Occasionally, the cells may also be confused with the blister cells or hemighosts formed in response to oxidative damage the key is whether there is a retained membrane wall (a blister) or no wall (a bite).




Causes
----
Microvascular damage: Disseminated intravascular coagulation (DIC) Thrombotic thrombocytopenic purpura (TTP) Renal disease particularly vasculitis Disseminated malignancy
 
Physical trauma Defective prosthetic heart valve with turbulent flow
<div style="width: 95%; overflow: auto; border: 1px solid navy; font-size:90%">
Red cell fragility e.g. iron deficiency or thalassaemia  
{| class="wikitable" style="color:black; background-color:#ffffff;" cellpadding="15"
Microvascular damage Removal of denatured haemoglobin arising in a range of conditions as below: oxidant damage (see also blister cells) Alpha thalassaemia Less commonly and in small numbers: liver disease, splenectomy
!colspan="1" |'''Microvascular damage'''
|-
|Disseminated intravascular coagulation (DIC), Thrombotic thrombocytopenic purpura (TTP), Renal disease particularly vasculitis, Disseminated malignancy
|-
!colspan="1"| '''Physical trauma'''
|-
|Particularly defective prosthetic heart valve or valve disease with turbulent flow
|-
!colspan="1"| '''Red cell fragility'''
|-
|e.g. iron deficiency, thalassaemia, megaloblastic anaemia, MDS (look for associated features)
|-
!colspan="1"| '''Removal of denatured haemoglobin'''
|-
|oxidant damage (see also blister cells) Alpha thalassaemia  
|-
!colspan="1"| '''Less commonly'''
|-
|Small numbers may occur in liver disease and splenectomy
|}
</div>


----


Clinical Examples Kt3.jpg 1.Clinical Image 1


'''Clinical Examples'''
'''Clinical Examples'''




Line 51: Line 69:




'''Clinical Image 1''':
<span style="font-style:italic; font-size:90%;'' >
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
'''''Clinical Image 1: '''Typical keratocyte forms, most have two horns surrounding a central depression. There are also some echinocytes present. Clinical diagnosis: Oxidative damage and Heinz body removal''
Typical keratocyte forms, most have two horns surrounding a central depression. There are also some echinocytes present. Clinical diagnosis: Oxidative damage and Heinz body removal
</span>
</div>
 


<gallery widths="250px" heights="250px" >
<gallery widths="250px" heights="250px" >
Line 61: Line 79:




''''Clinical Image 2:'''
<span style="font-style:italic; font-size:90%;'' >
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
'''''Clinical Image 2: '''Further typical keratocyte forms, note a cell with three horns (*) surrounding two central depressions. Here there is more extensive evidence of additional erythrocyte damage – (echinocytes, spherocytes and early fragments) and absent platelets. Clinical diagnosis: Thrombotic thrombocytopenic purpura''
Further typical keratocyte forms, note a cell with three horns (*) surrounding two central depressions. Here there is more extensive evidence of additional erythrocyte damage – (echinocytes, spherocytes and early fragments) and absent platelets. Clinical diagnosis: Thrombotic thrombocytopenic purpura
</span>
</div>




Line 72: Line 89:




'''Clinical Image 3:'''
<span style="font-style:italic; font-size:90%;'' >
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
'''''Clinical Image 3: '''In this case damage is considerable, and typical keratocytes are no longer present – being replaced by fragmented cells, however same pathological origin can still be detected with residual bites and horns. Note also the polychromatic cells formed by the marrow response to cell destruction. Clinical diagnosis: Thrombotic thrombocytopenic purpura''
In this case damage is considerable, and typical keratocytes are no longer present – being replaced by fragmented cells, however same pathological origin can still be detected with residual bites and horns. Note also the polychromatic cells formed by the marrow response to cell destruction. Clinical diagnosis: Thrombotic thrombocytopenic purpura
</span>
</div>
 
----
 


'''Pathobiology'''
The horn-like paired projections are caused by trauma to the cell; this is most commonly caused by slicing of the cell by fibrin strands within the microvasculature. The damage is followed by repair through spontaneous membrane fusion forming a pseudovacuole; this fragile structure rapidly ruptures giving rise to the characteristic appearance of a concave defect, with surrounding horns that are the residual walls of the vacuole.
Pitfalls The appearance of the keratocyte is characteristic. However, there are two potential sources of confusion: first when multiple horns are present on the cell, where they need to be distinguished from echinocytes or acanthocytes: look for the characteristic depression between the horns. When damage is more severe the keratocytes become increasingly irregular, form small sharp-edged fragments which can usually be detected. Occasionally, the cells may also be confused with the blister cells or hemighosts formed in response to oxidative damage the key is whether there is a retained membrane wall (a blister) or no wall (a bite).
----
----

Latest revision as of 15:53, 4 April 2023

(horned cells, bite cells, helmet cells)

Derivation: Latin Kerat (horn)


Appearance

Keratocytes usually have a single pair of spicules (hence the name horned cells); these generally frame a concave area of cell membrane, this gives rise to the alternative name of bite cell. Sometimes more than two "horns" are present and a gradual progression to fragments may be seen.



Images: Note the two typical horns surrounding a central depression in the drawn image - the origin as a vacuole that has ruptured (see Pathogenesis) is easy to imagine. The cartoon image shows one typical keratocyte (arrowed), but also emphasises the more widespread damage that ofetn accompany these forms with other damaged cells and precursor red cells present.



Significance

The presence of keratocytes always implies the mechanical destruction of erythrocytes and is therefore highly significant and often requires urgent reporting. In some (although not all) cases, the pathological process may be life threatening particularly if they are associated with disseminated intravascular coagulation (DIC) or thrombotic thrombocytopenic purpura (TTP) knowledge of platelet count, clotting and additional morphological features such as fragments is essential.

Pitfalls

The keratocyte istself is quite distinctive, however be aware of the range of causes that are not limited to microvascular damage. The appearance may also be a sign of ocidative damage or Heinz body removal. Careful attention to other features is important.



Microvascular damage
Disseminated intravascular coagulation (DIC), Thrombotic thrombocytopenic purpura (TTP), Renal disease particularly vasculitis, Disseminated malignancy
Physical trauma
Particularly defective prosthetic heart valve or valve disease with turbulent flow
Red cell fragility
e.g. iron deficiency, thalassaemia, megaloblastic anaemia, MDS (look for associated features)
Removal of denatured haemoglobin
oxidant damage (see also blister cells) Alpha thalassaemia
Less commonly
Small numbers may occur in liver disease and splenectomy


Clinical Examples



Clinical Image 1: Typical keratocyte forms, most have two horns surrounding a central depression. There are also some echinocytes present. Clinical diagnosis: Oxidative damage and Heinz body removal



Clinical Image 2: Further typical keratocyte forms, note a cell with three horns (*) surrounding two central depressions. Here there is more extensive evidence of additional erythrocyte damage – (echinocytes, spherocytes and early fragments) and absent platelets. Clinical diagnosis: Thrombotic thrombocytopenic purpura



Clinical Image 3: In this case damage is considerable, and typical keratocytes are no longer present – being replaced by fragmented cells, however same pathological origin can still be detected with residual bites and horns. Note also the polychromatic cells formed by the marrow response to cell destruction. Clinical diagnosis: Thrombotic thrombocytopenic purpura



Pathobiology

The horn-like paired projections are caused by trauma to the cell; this is most commonly caused by slicing of the cell by fibrin strands within the microvasculature. The damage is followed by repair through spontaneous membrane fusion forming a pseudovacuole; this fragile structure rapidly ruptures giving rise to the characteristic appearance of a concave defect, with surrounding horns that are the residual walls of the vacuole. Pitfalls The appearance of the keratocyte is characteristic. However, there are two potential sources of confusion: first when multiple horns are present on the cell, where they need to be distinguished from echinocytes or acanthocytes: look for the characteristic depression between the horns. When damage is more severe the keratocytes become increasingly irregular, form small sharp-edged fragments which can usually be detected. Occasionally, the cells may also be confused with the blister cells or hemighosts formed in response to oxidative damage the key is whether there is a retained membrane wall (a blister) or no wall (a bite).