adrenal mass Flashcards
Glomerulosa producing
fasciculata producing
reticularis producing
medulla
aldo
cortisol
androgens
catecholamines
how often are incidentalomas present in people over 50
3% of the time
If timor is >6cm then more likely
a malignancy 25% chance
80 % of incidentalomas are
<2 cm
In order what proportion of adrenal masses are functional?
1- cushing’s 9%
2- pheos 4%
3 - primary hyperaldo 1.5%
If adrenal tumour is secreting hormones then
stabilize and go to Sx
If adrenal tumour is not secreting hormones
check if tumor is >4 cm
- surgery unless it’s a met
Would you biopsy an adrenal mass?
NEVER until RO pheo
classic pheochromocytoma triad
Pain
Palpitation
Perspiration
(50% of patients)
how do you diagnose a pheo
- measure catecholamines
metanephrines and creatinine
Screenig for hyperaldo
Ratio of aldo to renin is high
a primary adrenal carcinoma can produce
High levels of androgens so perform DHEAS
Screening for adrenal hormone excess
1- creatinine, catechol, metane
2- Dex suppression test
3- aldo/renin ratio
Causes of unsuppressed cortisol if ACTH is high
- Pituitary ACTH, ectopic ACTH, ectopic CRH
-
Causes of unsuppressed cortisol if ACTH is low
Adrenal related
Cortisol levels if suspecting CUshing’s
Normally 3x ULN
And High dose DST - will not suppress cortisol
Tumors of adrenal cortex
- hyperplasias
- adenomas
- carcinomas
Tumors of adrenal medulla
pheos
- medullary hyperplasias
If suspecting cortical hyperplasia often bilaterial
- ACTH producing pituitary adenoma
- exogenous acth
- CRH producing tuor
How will contralateral adrenal gland look like if adrenal cortical adenoma suspected?
- will be atrophic –> addisonian crisis
Most common situation for increased mineralocorticoids
- adrenal cortical adenoma is most common
-
what would aldo-producing adenomas look like
lots of lipids - very yellow
Virilism or feminization think of
adrenal cortical carcinoma - may be present only with increased aldo or glue
Adrenal cortical carcinomas are often
LARGE
necrosis, invasive
NON-functioning or clinically functioning
Adrenal medullary hyperplasia often associated with
MEN2A MEN2B syndromes
Pheochromocytoma often
30% related to familial syndromes
Adenomas are most common with
Cushing’s and Conn’s syndromes