Hypertrophied column of Bertin

Changed by Alexandra Stanislavsky, 17 Nov 2015

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A column of Bertin is the extension of renal cortical tissue which separates the pyramids, and as such are normal structures. They become of radiographic importance when they are unusually enlarged an may be mistaken for a renal mass (renal pseudotumour).

Nomenclature of such enlarged columns is a little confusing, sometimes referred to as septa (although this may also refer to normal columns). Ideally the term hypertrophied column of Bertin or prominent column of Bertin should be used to avoid confusion.

Epidemiology

Columns of Bertin are present in ~50% of the healthy population and in 20% are bilateral. Double columns of Bertin in one kidney is less common, occuring in only 4% 5.

Hypertrophied columns of Bertin are more commonly bilateral, occuring in 60% 5

Embryology

The kidneys are formed from the fusion of multiple lobules, each containing a central core of medullary tissue surrounded by a mantle of cortex. Fusion of adjacent lobules leads to cortical tissue remaining between the pyramids, each column formed by the fusion of two layers of cortex 2. They are thus located beneath foetalfetal lobulations (usually not visible in adults).

Radiographic features

Key to correct identification of a hypertrophied column of Bertin is that fact that it is in continuity with, and of similar appearance to, normal renal cortical parenchyma, and that the renal outline is preserved.

They are usually located in the mid-portion of the kidney and are more commonly found on the left side 4.

Plain film urography

During intravenous urography septa of Bertin may mimic a mass by splaying and distorting the calyces. The renal outline however is normal (which is usually not the case when a renal cell carcinoma is present) and a slight indentation overlying the column may be seen representing location of previous foetalfetal lobulation.

Invariably the diagnosis should be confirmed with CT or MRI.

Ultrasound

Appearances on ultrasound can be confusing, however in general the echogenicity of the pseudomass is homogeneous and continuous with renal cortex. The mass has been described as "splitting" or "indenting" the renal sinus.

Often the diagnosis should be confirmed with CT or MRI, or more recently with contrast enhanced sonography, demonstrating similar enhancement as normal cortex. 

CT and MRI

CT and MRI are definitive demonstrating the hypertrophied column to have imaging features identical to that of adjacent normal cortex.

On non-contrast CT they appear isodense to normal parenchyma and, following administration of contrast, enhance uniformly with renal cortex, and remain isodense to normal parenchyma on delayed images. 

Similarly on MRI they appear isointense to cortex on all sequences and enhance similarly 4.

History and etymology

Named after Exupere Joseph Bertin, French anatomist who initially described such morphology in renal anatomy in 1744 2-3.

Differential diagnosis

The differential is essentially that of all renal masses and renal pseudotumours, and includes:

  • -<p>A <strong>column of Bertin</strong> is the extension of renal cortical tissue which separates the pyramids, and as such are normal structures. They become of radiographic importance when they are unusually enlarged an may be mistaken for a renal mass (<a href="/articles/renal-pseudotumour">renal pseudotumour</a>).</p><p>Nomenclature of such enlarged columns is a little confusing, sometimes referred to as septa (although this may also refer to normal columns). Ideally the term <strong>hypertrophied column of Bertin</strong> or <strong>prominent column of Bertin</strong> should be used to avoid confusion.</p><h4>Epidemiology</h4><p>Columns of Bertin are present in ~50% of the healthy population and in 20% are bilateral. Double columns of Bertin in one <a href="/articles/kidneys">kidney</a> is less common, occuring in only 4% <sup>5</sup>.</p><p>Hypertrophied columns of Bertin are more commonly bilateral, occuring in 60% <sup>5</sup>. </p><h4>Embryology</h4><p>The <a href="/articles/kidneys">kidneys</a> are formed from the fusion of multiple lobules, each containing a central core of medullary tissue surrounded by a mantle of cortex. Fusion of adjacent lobules leads to cortical tissue remaining between the pyramids, each column formed by the fusion of two layers of cortex <sup>2</sup>. They are thus located beneath foetal lobulations (usually not visible in adults).</p><h4>Radiographic features</h4><p>Key to correct identification of a hypertrophied column of Bertin is that fact that it is in continuity with, and of similar appearance to, normal renal cortical parenchyma, and that the renal outline is preserved.</p><p>They are usually located in the mid-portion of the kidney and are more commonly found on the left side <sup>4</sup>.</p><h5>Plain film urography</h5><p>During intravenous urography septa of Bertin may mimic a mass by splaying and distorting the calyces. The renal outline however is normal (which is usually not the case when a <a href="/articles/renal-cell-carcinoma-1">renal cell carcinoma</a> is present) and a slight indentation overlying the column may be seen representing location of previous foetal lobulation.</p><p>Invariably the diagnosis should be confirmed with CT or MRI.</p><h5>Ultrasound</h5><p>Appearances on ultrasound can be confusing, however in general the echogenicity of the pseudomass is homogeneous and continuous with renal cortex. The mass has been described as "splitting" or "indenting" the renal sinus.</p><p>Often the diagnosis should be confirmed with CT or MRI, or more recently with contrast enhanced sonography, demonstrating similar enhancement as normal cortex. </p><h5>CT and MRI</h5><p>CT and MRI are definitive demonstrating the hypertrophied column to have imaging features identical to that of adjacent normal cortex.</p><p>On non-contrast CT they appear isodense to normal parenchyma and, following administration of contrast, enhance uniformly with renal cortex, and remain isodense to normal parenchyma on delayed images. </p><p>Similarly on MRI they appear isointense to cortex on all sequences and enhance similarly <sup>4</sup>.</p><h4>History and etymology</h4><p>Named after <strong>Exupere Joseph Bertin</strong>, French anatomist who initially described such morphology in renal anatomy in 1744 <sup>2-3</sup>.</p><h4>Differential diagnosis</h4><p>The differential is essentially that of all <a href="/articles/renal-masses">renal masses</a> and <a href="/articles/renal-pseudotumour">renal pseudotumours</a>, and includes:</p><ul>
  • +<p>A <strong>column of Bertin</strong> is the extension of renal cortical tissue which separates the pyramids, and as such are normal structures. They become of radiographic importance when they are unusually enlarged an may be mistaken for a renal mass (<a href="/articles/renal-pseudotumour">renal pseudotumour</a>).</p><p>Nomenclature of such enlarged columns is a little confusing, sometimes referred to as septa (although this may also refer to normal columns). Ideally the term <strong>hypertrophied column of Bertin</strong> or <strong>prominent column of Bertin</strong> should be used to avoid confusion.</p><h4>Epidemiology</h4><p>Columns of Bertin are present in ~50% of the healthy population and in 20% are bilateral. Double columns of Bertin in one <a href="/articles/kidneys">kidney</a> is less common, occuring in only 4% <sup>5</sup>.</p><p>Hypertrophied columns of Bertin are more commonly bilateral, occuring in 60% <sup>5</sup>. </p><h4>Embryology</h4><p>The <a href="/articles/kidneys">kidneys</a> are formed from the fusion of multiple lobules, each containing a central core of medullary tissue surrounded by a mantle of cortex. Fusion of adjacent lobules leads to cortical tissue remaining between the pyramids, each column formed by the fusion of two layers of cortex <sup>2</sup>. They are thus located beneath fetal lobulations (usually not visible in adults).</p><h4>Radiographic features</h4><p>Key to correct identification of a hypertrophied column of Bertin is that fact that it is in continuity with, and of similar appearance to, normal renal cortical parenchyma, and that the renal outline is preserved.</p><p>They are usually located in the mid-portion of the kidney and are more commonly found on the left side <sup>4</sup>.</p><h5>Plain film urography</h5><p>During intravenous urography septa of Bertin may mimic a mass by splaying and distorting the calyces. The renal outline however is normal (which is usually not the case when a <a href="/articles/renal-cell-carcinoma-1">renal cell carcinoma</a> is present) and a slight indentation overlying the column may be seen representing location of previous fetal lobulation.</p><p>Invariably the diagnosis should be confirmed with CT or MRI.</p><h5>Ultrasound</h5><p>Appearances on ultrasound can be confusing, however in general the echogenicity of the pseudomass is homogeneous and continuous with renal cortex. The mass has been described as "splitting" or "indenting" the renal sinus.</p><p>Often the diagnosis should be confirmed with CT or MRI, or more recently with contrast enhanced sonography, demonstrating similar enhancement as normal cortex. </p><h5>CT and MRI</h5><p>CT and MRI are definitive demonstrating the hypertrophied column to have imaging features identical to that of adjacent normal cortex.</p><p>On non-contrast CT they appear isodense to normal parenchyma and, following administration of contrast, enhance uniformly with renal cortex, and remain isodense to normal parenchyma on delayed images. </p><p>Similarly on MRI they appear isointense to cortex on all sequences and enhance similarly <sup>4</sup>.</p><h4>History and etymology</h4><p>Named after <strong>Exupere Joseph Bertin</strong>, French anatomist who initially described such morphology in renal anatomy in 1744 <sup>2-3</sup>.</p><h4>Differential diagnosis</h4><p>The differential is essentially that of all <a href="/articles/renal-masses">renal masses</a> and <a href="/articles/renal-pseudotumour">renal pseudotumours</a>, and includes:</p><ul>
  • -<li>altered vascularity or enhancement</li>
  • +<li>altered vascularity or enhancement</li>

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