Genetic |
Tumor |
Isolated ACTH deficiency
|
Non-functioning pituitary adenoma |
POMC mutation/cleavage defect |
Functional pituitary adenoma |
Mutations in POMC transcription factors (TBX19) |
Craniopharyngioma |
Pituitary metastases |
Associated with other pituitary deficiencies
|
Germinoma |
PROP1, LHX3, LHX4, HESX1, OTX2 mutations |
Other tumours including astrocytoma, meningioma. |
Midline Defects |
Iatrogenic |
Septo-optic dysplasia (without HESX1 mutation) |
Exogenous glucocorticoids |
Pituitary surgery |
Cranial irradiation |
Post-treatment for hypercortisolism |
Opiates |
|
Infiltrative |
Neurosarcoidosis |
Histiocytosis X |
Haemochromatosis |
|
Inflammatory/Infective |
Hypophysitis (lymphocytic, granulomatous) |
Post-basal meningitis, abscesses, encephalitis. |
|
Traumatic/vascular |
Traumatic brain injury |
Subarachnoid haemorrhage |
Sheehan’s syndrome |
|
Miscellaneous |
Idiopathic |
Pituitary apoplexy |
Empty sella syndrome |
Rathkes cleft cyst |