In the past, endocrinologists typically treated patients with obvious disease. Primary hyperparathyroidism often presented with osteitis fibrosa cystica ( 1. Silverberg S.J. Bilezikian J.P. Evaluation and management of primary hyperparathyroidism. J Clin Endocrinol Metab. 1996; 81: 2036-2040 Crossref PubMed Google Scholar ). Cushing syndrome usually presented with rapid weight gain, proximal muscle weakness, and wide, violaceous striae ( 2. Newell-Price J. Bertagna X. Grossman A.B. Nieman L.K. Cushing's syndrome. Lancet. 2006; 367: 1605-1617 Abstract Full Text Full Text PDF PubMed Scopus (1026) Google Scholar ). Paget's disease mostly presented with skeletal pain ( 3. Altman R.D. Musculoskeletal manifestations of Paget's disease of bone. Arthritis Rheum. 1980; 23: 1121-1127 Crossref PubMed Scopus (97) Google Scholar ). These patients lived on the extreme end of the disease spectrum, where surgery or medications had a high likelihood of affecting their symptoms. Patients and their endocrinologists rarely struggled with whether or not to intervene. Not intervening usually led to a gradual worsening of their symptoms, with little hope for a spontaneous recovery. Thus, all of these patients could potentially benefit from intervention. With the advance of surgical techniques (e.g., transsphenoidal pituitary resection for pituitary tumors) and pharmaceuticals (e.g., insulin for diabetes and thionamides for hyperthyroidism), interventions promised disease improvement, if not a complete cure. Indeed, extreme manifestations of endocrinologic disease continue to exist. Conditions like thyroid storm, hypertensive crisis from pheochromocytoma, and diabetic ketoacidosis still need to be addressed with rapidity and skill, with a hope for full recovery with intervention and a high mortality rate otherwise.
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