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DIG is a large, cystic tumor of infancy that involves the superficial cerebral cortex and leptomeninges, and is composed of neoplastic astrocytes and neuronal components within a prominent desmoplastic stroma. DIG is considered a WHO Grade I tumor.


DIG is a rare tumor of infancy. The age range extends from 1-24 months, though non-infantile cases have been reported. There is a male predominance (1.7:1). DIG may be associated with cortical dysplasia.


DIG is a supratentorial lesion that commonly involves more than one lobe.

Clinical presentation

Symptoms are of short duration and include findings consistent with increased intracranial pressure.


MRI demonstrates a hypointense cytic mass with an isointense peripheral solid component that shows contrast-enhancement.


DIG are large tumors composed of deep multi-loculated cysts filled with clear or xanthochromic fluid. The superficial component is primarily extracerebral and is commonly attached to the dura.


DIG is composed of a variable mix of neoplastic astrocytes and neuronal elements within a prominent, reticulin-rich desmoplastic stroma. There is a sharp demarcation between the tumor and the cortical surface, though Virhcow-Robin spaces in the underlying cortex are often filled with tumor cells.

Molecular genetics

The molecular genetics of DIG have not been elucidated.


DIG is a surgically curable disease.

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