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. 2021 Feb 25;65(2):212–230. doi: 10.20945/2359-3997000000335

Table 2. Main etiologies of acquired hypopituitarism (adapted from Reference 28).

Etiologies of Acquired Hypopituitarism
Traumatic Tumors
Prior surgery Pituitary adenoma
Radiotherapy Empty sella
Traumatic brain injury Parasellar tumors or cysts
Infiltrating/Inflammatory Rathke’s cyst
Primary hypophysitis Dermoid cyst
Lymphocytic Meningioma
Granulomatous Germinoma
Xanthomatous Chordoma
Secondary hypophysitis Ependymoma
Sarcoidosis Glioma
Granulomatosis with polyangiitis Pinealoma
Langerhans cell histiocytosis Craniopharyngioma
Infection Hypothalamic hamartomas
Hemochromatosis Gangliocytoma
Amyloidosis Metastasis
Pituitary abscess Hematological malignancies
PIT-1 antibody Leukemias
Lymphomas
Associated with infections Functional
Tuberculosis Nutritional
Syphilis Excessive physical activity
Pneumocystis jirovecii Serious diseases
Fungi (histoplasmosis, aspergillosis) Acute diseases
Parasites (toxoplasmosis) Chronic renal failure
Viruses (cytomegalovirus) Chronic hepatic failure
Hormonal
Hyperprolactinemia
Primary hypothyroidism
Vascular Drug-induced dysfunctions
Related to pregnancy (Sheehan’s syndrome) Glucocorticoids
Dopamine agonists
Aneurismal subarachnoid hemorrhage Somatostatin analogs
Pituitary apoplexy Retinoids
Diabetes Anti-PD-1 monoclonal antibodies
Hypotension Anti-CTLA-4 monoclonal antibodies
Arteritis Opioids
Anticonvulsants