Pituicytoma

MONDO:0006372

An extremely rare, WHO grade I, circumscribed and slow-growing tumor that arises from the neurohypophysis or infundibulum and described in adults. It is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements. Signs and symptoms include visual disturbances, headache, amenorrhea, and decreased libido.

Also known as: pituicytoma, pituicytoma (WHO grade I), posterior pituitary astrocytoma, PTCY

2763 clinical trials for this condition and its sub-types.

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