This is a case of autoimmune polyglandular syndrome, type II with lymphocytic hypophysitis (LYH) of autoimmune pathogenesisin a 23-year-old boy, who presented with hypotension and bouts of hypoglycaemia. The patient was noted to have multipleendocrine involvement like thyroid, pancreas, adrenals besides pituitary gland. Presentation of the disease in a male patient, as inthis case report, is even more uncommon, and for this reason it merits reporting
展开▼
