Dysembryoplastic neuroepithelial tumor (DNET)

Case contributed by Frank Gaillard , 23 Feb 2010
Diagnosis certain
Changed by Frank Gaillard, 29 May 2018

Updates to Case Attributes

Body was changed:

25 year old woman with intractable epilepsyThe patient went on to have a resection.

Histology

Sections show brain tissue, including cerebral cortex and white matter, with areas of a relatively localized and superficial low-grade glial tumour. The tumour cells are fibrillar, and in areas display a bipolar appearance. There is a propensity for perivascular localization with nuclear-free zones between vessels. Mitotic activity is not increased. Vascular neurogenesis is not seen. Necrosis is not evident. Some areas display a loose hypocellular and cystic background. Small microcystic areas are also focally evident. Individual tumour cells are round to oval-shaped, and elongated, depending on the orientation. Some granular bodies are seen. Floating neurons are not well-defined, although entrapped neurons are observed within several parts of the tumour. In some areas, the pattern of architectural arrangement of neurons is irregular, consistent with focal cortical dysplasia. A ganglion cell component of a ganglioglioma is not definitively excluded.

Final Diagnosis

Brain, orbital frontal cortexFINAL DIAGNOSISdysembryoplastic neuroepithelial tumour (DNET).

  • -<p>25 year old woman with intractable epilepsy. </p><p>Sections show brain tissue, including cerebral cortex and white matter, with areas of a relatively localized and superficial low-grade glial tumour. The tumour cells are fibrillar, and in areas display a bipolar appearance. There is a propensity for perivascular localization with nuclear-free zones between vessels. Mitotic activity is not increased. Vascular neurogenesis is not seen. Necrosis is not evident. Some areas display a loose hypocellular and cystic background. Small microcystic areas are also focally evident. Individual tumour cells are round to oval-shaped, and elongated, depending on the orientation. Some granular bodies are seen. Floating neurons are not well-defined, although entrapped neurons are observed within several parts of the tumour. In some areas, the pattern of architectural arrangement of neurons is irregular, consistent with <a href="/articles/focal-cortical-dysplasia" title="focal cortical dysplasia">focal cortical dysplasia</a>. A ganglion cell component of a ganglioglioma is not definitively excluded.</p><p>Final Diagnosis</p><p>Brain, orbital frontal cortex: <a href="/articles/dysembryoplastic-neuroepithelial-tumour" title="Dysembryoplastic neuroepithelial tumour">Dysembryoplastic neuroepithelial tumour</a>.</p>
  • +<p>The patient went on to have a resection. </p><p><strong>Histology</strong></p><p>Sections show brain tissue, including cerebral cortex and white matter, with areas of a relatively localized and superficial low-grade glial tumour. The tumour cells are fibrillar, and in areas display a bipolar appearance. There is a propensity for perivascular localization with nuclear-free zones between vessels. Mitotic activity is not increased. Vascular neurogenesis is not seen. Necrosis is not evident. Some areas display a loose hypocellular and cystic background. Small microcystic areas are also focally evident. Individual tumour cells are round to oval-shaped, and elongated, depending on the orientation. Some granular bodies are seen. Floating neurons are not well-defined, although entrapped neurons are observed within several parts of the tumour. In some areas, the pattern of architectural arrangement of neurons is irregular, consistent with <a href="/articles/focal-cortical-dysplasia">focal cortical dysplasia</a>. A ganglion cell component of a ganglioglioma is not definitively excluded.</p><p>FINAL DIAGNOSIS: <a href="/articles/dysembryoplastic-neuroepithelial-tumour">dysembryoplastic neuroepithelial tumour (DNET)</a>.</p>
Suitable For Quiz was set to .

Updates to Study Attributes

Findings was changed:

A lesion on the inferior surface of the left frontal lobe is characterised by high T2 signal in the subcortical white matter with minor intrinsic high T1 signal and no discernable contrast enhancement.

Images Changes:

Image MRI (T1) ( update )

Perspective was set to Sagittal.
Single Or Stack Root was set to .
Description was removed:
DNET : T1

Image MRI (T1 C+) ( update )

Perspective was set to Sagittal.
Single Or Stack Root was set to .
Description was removed:
DNET : T1 C+

Image MRI (DWI) ( update )

Perspective was set to Axial.
Single Or Stack Root was set to .
Description was removed:
DNET : DWI

Image MRI (T2) ( update )

Perspective was set to Axial.
Description was removed:
DNET : T2

Image MRI (T2) ( update )

Perspective was set to Coronal.
Description was removed:
DNET : T2

Image MRI (T1) ( update )

Perspective was set to Axial.
Description was removed:
DNET : T1

Image MRI (T1 C+) ( update )

Perspective was set to Axial.
Description was removed:
DNET : T1 C+

Image 1 MRI (T2) ( update )

Position was set to .

Image 2 MRI (T2) ( update )

Position was set to .

Image 3 MRI (T1) ( update )

Position was set to .

Image 4 MRI (T1 C+) ( update )

Position was set to .

Image 5 MRI (T1) ( update )

Position was set to .

Image 7 MRI (DWI) ( update )

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