Hemorrhage on MRI
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The imaging characteristics of blood on MRI are variable and change with the age of the blood.
In general, five stagesof haematoma evolution are recognised:
-
hyperacute
- intracellular oxyhaemoglobin
- isointense on T1
- isointense to hyperintense on T2
-
acute (1 to 2 days)
- intracellular deoxyhaemoglobin
- T2 signal intensity drops (T2 shortening)
- T1 remains intermediate-to-long
-
early subacute (2 to 7 days)
- intracellular methaemoglobin
- T1 signal gradually increases (T1 shortening) to become hyperintense
-
late subacute (7 to 14-28 days)
- extracellular methaemoglobin: over the next few weeks, as cells break down, extracellular methaemoglobin leads to an increase in T2 signal
-
chronic (>14-28 days)
- periphery
- intracellular haemosiderin
- low on both T1 and T2
- center
- extracellular hemichromes
- isointense on T1, hyperintense on T2
- periphery
Practical points
- extracranial blood products age differently than intracranial blood products, and extracranial hematomas often have a heterogeneous appearance, confounding attempts at reliably dating the age of an extracranial hemorrhage 3,4
See also
-<p>The imaging characteristics of <strong>blood on MRI</strong> are variable and change with the age of the blood.</p><p>In general, five stages<strong> </strong>of haematoma evolution are recognised:</p><ol>-<li>-<strong>hyperacute </strong><ul>-<li>intracellular oxyhaemoglobin</li>-<li>isointense on T1</li>-<li>isointense to hyperintense on T2</li>-</ul>-</li>-<li>-<strong>acute</strong> (1 to 2 days)<ul>-<li>intracellular deoxyhaemoglobin</li>-<li>T2 signal intensity drops (T2 shortening)</li>-<li>T1 remains intermediate-to-long</li>-</ul>-</li>-<li>-<strong>early subacute</strong> (2 to 7 days)<ul>-<li>intracellular methaemoglobin</li>-<li>T1 signal gradually increases (T1 shortening) to become hyperintense</li>-</ul>-</li>-<li>-<strong>late subacute</strong> (7 to 14-28 days)<ul><li>extracellular methaemoglobin: over the next few weeks, as cells break down, extracellular methaemoglobin leads to an increase in T2 signal </li></ul>-</li>-<li>-<strong>chronic</strong> (>14-28 days)<ul>-<li>periphery<ul>-<li>intracellular haemosiderin</li>-<li>low on both T1 and T2</li>-</ul>-</li>-<li>center<ul>-<li>extracellular hemichromes</li>-<li>isointense on T1, hyperintense on T2</li>-</ul>-</li>-</ul>-</li>-</ol><h4>Practical points</h4><ul><li>extracranial blood products age differently than intracranial blood products, and extracranial hematomas often have a heterogeneous appearance, confounding attempts at reliably dating the age of an extracranial hemorrhage <sup>3,4</sup>-</li></ul>- +<p>The imaging characteristics of <strong>blood on MRI</strong> are variable and change with the age of the blood.</p><p>In general, five stages<strong> </strong>of haematoma evolution are recognised:</p><ol>
- +<li>
- +<strong>hyperacute </strong><ul>
- +<li>intracellular oxyhaemoglobin</li>
- +<li>isointense on T1</li>
- +<li>isointense to hyperintense on T2</li>
- +</ul>
- +</li>
- +<li>
- +<strong>acute</strong> (1 to 2 days)<ul>
- +<li>intracellular deoxyhaemoglobin</li>
- +<li>T2 signal intensity drops (T2 shortening)</li>
- +<li>T1 remains intermediate-to-long</li>
- +</ul>
- +</li>
- +<li>
- +<strong>early subacute</strong> (2 to 7 days)<ul>
- +<li>intracellular methaemoglobin</li>
- +<li>T1 signal gradually increases (T1 shortening) to become hyperintense</li>
- +</ul>
- +</li>
- +<li>
- +<strong>late subacute</strong> (7 to 14-28 days)<ul><li>extracellular methaemoglobin: over the next few weeks, as cells break down, extracellular methaemoglobin leads to an increase in T2 signal </li></ul>
- +</li>
- +<li>
- +<strong>chronic</strong> (>14-28 days)<ul>
- +<li>periphery<ul>
- +<li>intracellular haemosiderin</li>
- +<li>low on both T1 and T2</li>
- +</ul>
- +</li>
- +<li>center<ul>
- +<li>extracellular hemichromes</li>
- +<li>isointense on T1, hyperintense on T2</li>
- +</ul>
- +</li>
- +</ul>
- +</li>
- +</ol><h4>Practical points</h4><ul><li>extracranial blood products age differently than intracranial blood products, and extracranial hematomas often have a heterogeneous appearance, confounding attempts at reliably dating the age of an extracranial hemorrhage <sup>3,4</sup>
- +</li></ul>
- +<h4>See also</h4><ul>
- +<li><a href="/articles/ageing-blood-on-mri-mneuomonic"> ageing blood on MRI (mnemonic)</a></li>
- +</ul>