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Microcytic and Hypochromic Red Cells: Difference between revisions

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(Created page with "'''Derivation:''' Eponymous: William Howell (US) and Justin Jolly (Fr) early morphologists studying effects of splenic absence '' ---- '''Appearance''' Small blue/purple fragments generally rounded – their colour and position reflects their origin as retained fragments of the cell nucleus that most often they are single and relatively centrally placed. They have relatively large size compared with other inclusions (usually 0.5-1.0μM in diameter compared with a typi...")
 
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'''Derivation:''' Eponymous: William Howell (US) and Justin Jolly (Fr) early morphologists studying effects of splenic absence ''
'''Derivation:''' ''From the Greek hypo [under} and New Latin chromia [state of pigmentation]''


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'''Appearance'''
'''Appearance'''  


Small blue/purple fragments generally rounded their colour and position reflects their origin as retained fragments of the cell nucleus that most often they are single and relatively centrally placed. They have relatively large size compared with other inclusions (usually 0.5-1.0μM in diameter compared with a typical erythrocyte diameter of 7.5M).  
A cell containing insufficient haemoglobin best detected as an increase when the area of pallor iof the erythrocyte extends beyond one third of the red cell diameter. The appearance tends to be obvious when the pallor exceeds half the cell diameter. In most circumstances hypochromic cells will also have reduced size (microcytosis).




 
<gallery mode="nolines" widths="240px" heights="240px" border="1px" >
<gallery widths="180px" heights="180px" >
File:HypoC1.png|link={{filepath:HypoC1.png}}
File:HJ1.png|link={{filepath:HJ1.png}}
File:HypoC2.jpg|link={{filepath:HypoC2.jpg}}
</gallery>
 
 
'''Image 1'''
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
In this case a single body is indicated – note the relatively large size, and purple colour. This example is offset from the centre but not peripheral – a fairly typical position for these inclusions.
</div>
 
 
 
<gallery widths="180px" heights="180px" >
File:HJ2.png|link={{filepath:HJ2.png}}
</gallery>
</gallery>




'''Image 2'''
<span style="font-style:italic; font-size:90%;'' >
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
'''Images''' The area of pallor in the center of the cell extends almost to the edge of the cell. The hypochromia indicates a reduced hemoglobin content. Hypochromatic cells are also generally small in size (microcytic). Note the small size (compare with the nucleus of the small lymphocyte).
In this case the Howell Jolly body as accompanied by a target cell as a feature indicating hyposplenism, other features of the hyposplenic state may include irregularly contracted cells or speculated cells (not shown here). Remember also to look for possible cause e.g. sickle cells.
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'''Significance'''
'''Significance'''


Howell-Jolly Bodies most commonly arise when spleen is absent or spleen function is impaired (hyposplenia). Occasional Howell Jolly bodies may arise in physiological conditions (see table).
The presence of hypochromia indicates defective production of haemoglobin. Most cases result from iron deficiency or thalassaemia – other typical features of these conditions should therefore be sought. Less frequently, hypochromia reflects defective iron utilisation (e.g. chronic disease or sideroblastic anaemia). The presence of hypochromia is not of itself an urgent problem unless there is severe anaemia; however, it important to highlight the condition since clinicians may need to request further investigation to determine its cause.




'''Pitfalls'''
'''Pitfalls'''


The group of conditions that have basophilic inclusions includes basophilic stippling and Pappenheimer bodies but these rarely cause any diagnostic confusion. Remember also however that (depending on the underlying condition) both Pappenheimer bodies and basophilic stippling may be found together with Howell Jolly bodies. More frequently, platelets or stain debris overlying red cells will cause confusion if there is doubt look for the typical colour and rounded nature, then compare them with any platelets or debris visible between red cells.
Be sure you are viewing the correct area of the film – the central pallor is clearly shown only in the area where red cells first begin to contact each other. Poorly stained films may also be a problem remember it is the extent of the area of pallor that is important not the stain colour. Finally, central pallor probably cannot be accurately assessed in damaged or abnormally shaped cells unless the hypochromia is very severe.
 
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'''Further information'''
 
1. [[Causes of Howell Jolly bodies''Go to Causes'']]
 
2. [[Clinical Examples: Howell Jolly bodies''Go to Clinical Examples]]
 
3. [[Pathobiology of Howell Jolly bodies|Go to Pathobiology]]




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'''Causes'''
<div style="width: 95%; overflow: auto; border: 1px solid navy; font-size:90%">
 
{| class="wikitable" style="color:black; background-color:#ffffff;" cellpadding="15"


<div style="width: 95%; overflow: auto; border: 2px solid navy; font-size:120%">
!'''DEFECTIVE IRON AVAILABILITY OR USAGE'''
{| class="wikitable" style="color:nay; background-color:#ffffff;" cellpadding="15"
!colspan="1"|'''HYPO'SPLENISM: Physiological'''
|-
|-
|Causes including normal i1ndividuals (very infrequent), pregnancy (infrequent), neonates (frequent) – more common in hyposplenic states
|Iron deficiency
|-
|-
!colspan="1''|'''HYPOSPLENISM: Pathological absence'''
|Anaemia of chronic disease
|-
|-
|Surgical or traumatic splenectomy, Auto-splenectomy (e.g. sickle cell disease), |Congenital asplenism,  
|Less commonly: Sideroblastic anaemia, Heavy metal poisoning
|-
|-
!colspan="|'''HYPOSPLENISM: Pathological hypofunction'''
!'''DISORDERS OF HAEMOGLOBIN'''
|-
|-
|Including: Normal neonates, Coeliac Disease, Bone marrow transplant, Pregnancy
|Thalassaemia syndromes: are the principle inherited cause of hypochromia (look for associated features)
|-
|-
|Other haemoglobinopathies: tend not to be hypochromic unless there is associated thalassaemia or iron deficiency. There may be a mild microcytosis.
|}
|}
</div>
</div>


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'''Clinical Examples'''


<gallery widths="250px" heights="250px" >
<gallery widths="250px" heights="250px" >
File:HJ3.jpg||link={{filepath:HJ3.jpg}}
File:HypoC3.jpg|link={{filepath:HypoC3.jpg}}
</gallery>
</gallery>




 
<span style="font-style:italic; font-size:90%;'' >
'''Clinical Image 1'''
'''Clinical Image 1: ''' Hypochromic microcytic red cells Note the small size in comparison to the nucleus of the small erythrocyte. The erythrocytes are variable in size (anisocytosis); however, the major feature is the hypochromia the area of central pallor extends to around 60-70% of the cell diameter. Clinical condition: iron deficiency
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
</span>
One almost central Howell Jolly body that is almost centrally placed – recognise by the size and colour. In this film there are also very frequent target cells and contracted cells. Clinical condition: HbSC disease with hyposplenic features 
</div>




<gallery widths="250px" heights="250px" >
<gallery widths="250px" heights="250px" >
File:HJ4.jpg||link={{filepath:HJ4.jpg}}
File:HypoC4.jpg|link={{filepath:HypoC4.jpg}}
</gallery>
</gallery>




<span style="font-style:italic; font-size:90%;'' >
'''Clinical Image 2''': Hypochromic microcytic red cells In this case the overall staining and background is more grey in shade; however the appearance is otherwise identical to the previous example. Two elongated pencil cells are also shown. Clinical condition: iron deficiency
</span>


'''Clinical Image 2:'''
<div class="toccolours mw-collapsible mw-collapsed" style="font-size 80%; overflow:auto;">
Very frequent Howell Jolly bodies in cells showing a range of other abnormal features (excessive variation in shape and size). Note the range of sizes and positions. Clinical condition: Post-splenectomy
</div>


<gallery widths="250px" heights="250px" >
<gallery widths="250px" heights="250px" >
File:HJ5.jpg||link={{filepath:HJ5.jpg}}
File:HypoC5.jpg|link={{filepath:HypoC5.jpg}}
</gallery>
</gallery>




'''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:''' Hypochromic microcytic red cells Note the variability in size although in most cases this is clearly reduced compared with the nucleus of the lymphocyte the hypochromia is much more difficult to detect as many of the cells are target cells; however, the rim of haemoglobin is very narrow. There is a single polychromatic cell and the edge of a nucleated red cell can be seen. Clinical condition: thalassaemia intermedia
A single cell containing a Howell Jolly body, in this case there are accompanying target cells, one “boat shaped” and several dense contracted cells. Clinical condition: sickle cell disease with hyposplenism (no true sickle cells are shown on this film).
</span>
</div>


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'''Pathobiology'''


'''Pathobiology'''
The biconcave disk shape of erythrocytes means that when flattened on a glass slide the central area of the cell appears pale; when the haemoglobin content of a red cell is reduced this pale area becomes more extensive. Reduced cellular haemoglobin generally arises either from reduced haem formation (particularly iron deficiency) or from reduced globin chain synthesis (thalassaemia).
 
 
When red cell formation is completed the nucleus is extruded. Before this the nuclear material becomes condensed (pyknosis) and often fragmented (karryohexis) leaving many separate remnants. Normally these nuclear remains are efficiently removed from circulating erythrocytes by the spleen, however if splenic function is impaired the fragments remain as Howell Jolly bodies.  


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Latest revision as of 19:22, 26 March 2023

Derivation: From the Greek hypo [under} and New Latin chromia [state of pigmentation]


Appearance

A cell containing insufficient haemoglobin – best detected as an increase when the area of pallor iof the erythrocyte extends beyond one third of the red cell diameter. The appearance tends to be obvious when the pallor exceeds half the cell diameter. In most circumstances hypochromic cells will also have reduced size (microcytosis).



Images The area of pallor in the center of the cell extends almost to the edge of the cell. The hypochromia indicates a reduced hemoglobin content. Hypochromatic cells are also generally small in size (microcytic). Note the small size (compare with the nucleus of the small lymphocyte).



Significance

The presence of hypochromia indicates defective production of haemoglobin. Most cases result from iron deficiency or thalassaemia – other typical features of these conditions should therefore be sought. Less frequently, hypochromia reflects defective iron utilisation (e.g. chronic disease or sideroblastic anaemia). The presence of hypochromia is not of itself an urgent problem unless there is severe anaemia; however, it important to highlight the condition since clinicians may need to request further investigation to determine its cause.


Pitfalls

Be sure you are viewing the correct area of the film – the central pallor is clearly shown only in the area where red cells first begin to contact each other. Poorly stained films may also be a problem – remember it is the extent of the area of pallor that is important not the stain colour. Finally, central pallor probably cannot be accurately assessed in damaged or abnormally shaped cells unless the hypochromia is very severe.



DEFECTIVE IRON AVAILABILITY OR USAGE
Iron deficiency
Anaemia of chronic disease
Less commonly: Sideroblastic anaemia, Heavy metal poisoning
DISORDERS OF HAEMOGLOBIN
Thalassaemia syndromes: are the principle inherited cause of hypochromia (look for associated features)
Other haemoglobinopathies: tend not to be hypochromic unless there is associated thalassaemia or iron deficiency. There may be a mild microcytosis.


Clinical Image 1: Hypochromic microcytic red cells Note the small size in comparison to the nucleus of the small erythrocyte. The erythrocytes are variable in size (anisocytosis); however, the major feature is the hypochromia the area of central pallor extends to around 60-70% of the cell diameter. Clinical condition: iron deficiency



Clinical Image 2: Hypochromic microcytic red cells In this case the overall staining and background is more grey in shade; however the appearance is otherwise identical to the previous example. Two elongated pencil cells are also shown. Clinical condition: iron deficiency



Clinical Image 3: Hypochromic microcytic red cells Note the variability in size although in most cases this is clearly reduced compared with the nucleus of the lymphocyte the hypochromia is much more difficult to detect as many of the cells are target cells; however, the rim of haemoglobin is very narrow. There is a single polychromatic cell and the edge of a nucleated red cell can be seen. Clinical condition: thalassaemia intermedia


Pathobiology

The biconcave disk shape of erythrocytes means that when flattened on a glass slide the central area of the cell appears pale; when the haemoglobin content of a red cell is reduced this pale area becomes more extensive. Reduced cellular haemoglobin generally arises either from reduced haem formation (particularly iron deficiency) or from reduced globin chain synthesis (thalassaemia).