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Title: Human adenohypophysis in Nelson syndrome. Ultrastructural and clinical study. Author: Garcia JH, Kalimo H, Givens JR. Journal: Arch Pathol Lab Med; 1976 May; 100(5):253-8. PubMed ID: 178289. Abstract: The manifestations that comprise the disease known as Nelson syndrome are pituitary hyperplasia and cutaneous hyperpigmentation, which sometimes follow bilateral adrenalectomy, in patients with hypercortisolism. We present a comprehensive endocrinologic, structural study of a patient in whom the evidence obtained supports the hypotheses that: (a) the primary disorder in this form of hypercortisolism is probably hypothalamic; (b) the hyperplasia of the adenohypophysis, following adrenalectomy, is closely associated with lowered plasma cortisol levels; and (c) the cillular hyperplasia in the adenohypophysis involves primarily the corticotroph, a cell believed to be associated with the secretion of adrenocorticotrophic hormone and melanocyte-stimulating hormone.[Abstract] [Full Text] [Related] [New Search]