From: Acute adrenal failure as the presenting feature of primary antiphospholipid syndrome in a child
Congenital | CAH |
---|---|
Congenital adrenal hypoplasia | |
ACTH resistance | |
Glucocorticoid resistance | |
Metabolic diseases (Adrenoleukodystrophy, Zellweger, Smith-Lemli-Opitz, Wolman disease) | |
Acquired | Autoimmune adrenalitis |
- Isolated | |
- Autoimmune polyendocrinopathy | |
- syndrome type 1 | |
- Autoimmune polyendocrinopathy syndrome type 2 | |
Hemorrhage/infarction | |
- Trauma | |
- Waterhouse-Frederickson syndrome | |
- Anticoagulation | |
- Thrombosis (APS, Thrombophilia) | |
Drug effects (Aminoglutethimide, mitotane, ketoconazole, medroxyprogesterone) | |
Infection | |
- Viral: HIV, cytomegalovirus | |
- Fungal: coccidiomycosis, histoplasmosis, blastomycosis, cryptococcosis | |
- Mycobacterial: tuberculosis | |
- Amebic | |
Infiltrative (Hemochromatosis, histiocytosis, sarcoidosis, amyloidosis, neoplasm) |