Pituitary and Sellar region masses Flashcards
Majority of sellar region masses
pituitary adenomas (85%) equiv to WHO grade I
Others are treated by surgical resection unless medical therapies available
Most uncommon: Rathke cleft cyst or sellar region masses (piuicytoma, spindle cell oncocytoma, hypophysistis) mimic pituitary adenomas on neuroimaging and mimic clinically non functioning pituitary adenomas (mass effect or visual disturbance)
Middle aged adults except craniopharyngioma (5-15 y and 45-60 y peaks)
Causes of pituitary adenoma
MEN (mult endocrine neoplasia)
AIP (familial isolated prolactinoma)
-above are in pediatric pop with germline mutation correlation
Families
Gonadotrophs: FSH/LH
Prolactin/TSH/GH
ACTH
Does size equal aggressiveness for pituitary tumors?
No
Most are still WHO grade I
Genes in pituitary tumors
MEN1
CDKN1B
PRKAR1A
AIP
Genes don’t play much of a role in SPORADIC forms
Intervention for pituitary adenomas (most common)
surgical intervention
Work-up of pituitary adenoma
H+E Reticulin CAM5.2 Synaptophysin (see packaging granules) PRL GH ACTH FSH Estrogen receptor
Prolactinomas in young women and ACTH adenomas are almost always
microadenomas
85%
Hormonally inactive (non-secretors) generally present with
sx of mass effects
HA Visual field deficits CN palsies -ptosis -diplopia
Pituitary hormone deficits
Panhypopituitarism
Rarely: seizures, stroke, CSF leak