Pituitary adenomas are tumors that
occur in the pituitary gland, and account for about
10% of intracranial neoplasms. They often remain undiagnosed,
and small pituitary tumors are found in 6 to 24 percent
of adults at autopsy.
The diagnosis is generally entertained either on
the basis of visual difficulties arising from the
compression of the optic nerve by the tumor, or on
the basis of manifestations of excess hormone secretion:
the specifics depend on the type of hormone. The specific
area of the visual pathway at which compression by
these tumours occurs is at the optic chiasma.
The anatomy of this structure causes pressure on it
to produce a defect in the temporal visual field on
both sides, a condition called bitemporal hemianopia.
Tumors which cause visual difficulty are likely to
be macroadenomata greater than 10 mm in diameter;
tumors less than 10 mm are microadenomata.
Some tumors secrete more than one hormone, the most
common combination being GH and prolactin.
Prolactinomas are frequently diagnosed during pregnancy,
when the hormone progesterone increases the tumor's
growth rate. Headaches may be present. The diagnosis
is confirmed by testing hormone levels, and by radiographic
imaging of the pituitary (for example, by CT scan
or MRI).
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