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. 2022 Jun 27;66(4):541–550. doi: 10.20945/2359-3997000000493

Table 2. Etiologies of central adrenal insufficiency.

Iatrogenic Procedure
Medication Hypothalamic and pituitary surgery
Glucocorticoids Radiosurgery and radiotherapy
Opiates
Megestrol acetate
Medroxyprogesterone
Immune checkpoint inhibitors
Hypophysitis Secondary hypophysitis
Infiltrative disease Sarcoid granulomatosis with polyangiitis
Hemochromatosis Langerhans cell histiocytosis
Amyloidosis Infection
PIT1-antibody
Primary hypophysitis
Lymphocytic
Granulomatous
Xanthomatous
Vascular
Sheehan’s syndrome
Aneurysmal subarachnoid hemorrhage
Pituitary apoplexy
Arteritis
Tumors
Pituitary abscess Ependymoma
Pituitary adenoma Glioma
Empty sella Pinealoma
Parasellar tumors or cysts Craniopharyngioma
Rathke’s cyst Hypothalamic hematoma
Dermoid cyst Gangliocytoma
Meningioma Metastasis
Germinoma Hematological malignancies (leukemias, lymphomas)
Chordoma
Traumatic
Head injury
Perinatal trauma
Genetic
Combined pituitary hormone deficiencies Associated syndromes
POUF1 Septooptic dysplasia ( HESX1 )
PROP1 GH, TSH, ACTH deficiencies and cerebellar abnormalities ( LHX4 )
Isolated ACTH deficiency Hypopituitarism and mental retardation ( SOX3 )
TBX19 (TPIT) Holoprosencephaly and multiple midline defects ( GLI2 )
POMC Anophthalmia, hypopituitarism, esophageal atresia ( SOX2 )
PC1(PCSK1) – POMC processing defect CHARGE syndrome
Prader-Willi syndrome
Idiopathic