A 40-year-old male with a past medical history of tobacco abuse and HIV presented to our hospital for cough, nausea, vomiting, and abdominal pain of 5-day duration. Upon arrival, the patient was afebrile, with a pulse rate of 104 and a blood pressure of 80/60. Chest radiography revealed a right lower lobe consolidation. Chest CT revealed right paratracheal adenopathy and a 5.8 × 4.5 cm mass occluding the bronchus intermedius (). CT of the abdomen and pelvis without contrast revealed dense bilateral adrenal masses, measuring 5.4 × 4.0 cm on the right and 4.8 × 2.0 cm on the left (). Laboratory studies were significant for a white blood cell count of 18.5 K/mm3, sodium of 131 mmol/L, creatinine of 1.6 mg/dL, and CD4 count of 567 cells/mm3. Due to concerns for sepsis, the patient was admitted to the hospitalist service, given IV fluids, and started on vancomycin and piperacillin/tazobactam empirically. Infectious workup included serum CMV, Influenza PCR, Mycoplasma and Bartonella IgG/IgM, Cryptococcus, Histoplasma, and Legionella urinary antigen that all returned negative. With ongoing hypotension while on antibiotics, a random morning cortisol level was ordered to evaluate for adrenal insufficiency. This returned at the lower limit of normal at 7.0 μg/dL. The ACTH stimulation test displayed an inappropriate response with cortisol levels at 30 minutes and 60 minutes of 10.1 μg/dL and 10.3 μg/dL, respectively. Serum ACTH was elevated at 83.4 pg/mL. MRI brain revealed no pituitary adenoma confirming the diagnosis of primary adrenal insufficiency. Stress dose steroids consisting of 100 mg intravenous hydrocortisone every 8 hours resulted in resolution of hypotension and abdominal pain. Adrenal function stabilized on 15 mg of oral prednisone in the morning and 5 mg in the evening. The adrenal CT washout study showed precontrast densities measuring 27, 54, and 61 Hounsfield units on the precontrast, portal venous phase, and delayed imaging on the right, respectively. The left adrenal gland measured 32, 48, and 51 Hounsfield units on precontrast, postcontrast, and delayed imaging, respectively, both consistent with metastatic disease. Pathology from the endobronchial mass and 4R lymph node biopsy revealed poorly differentiated neuroendocrine carcinoma confirming SCLC (see below). The patient started inpatient radiation therapy to his lung mass followed by outpatient chemotherapy. Two rounds of palliative chest radiation with 8 Gy resulted in a significant decrease in the size of the primary mass and relief of obstruction ()., Lung cancer spread to the adrenal glands (adrenal metastases) is common. This article explores the symptoms, treatment options, and what this means in terms of your prognosis. A 2018 study found that, although survival was poorer for those with non-small cell lung cancer who underwent the procedure than with some other cancers, image-guided , Although lung cancer does metastasize to the adrenal gland, adrenal insufficiency is rare, as greater than 90% of the functional cortex must be destroyed for this to occur . In one retrospective study spanning 30 years with 464 patients with adrenal metastatic disease from various tumors, only five of these patients developed adrenal .