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The endocrinopathy of POEMS syndrome
P M Stewart1, M A McIntyre, C R Edwards
1Department of Medicine, Western General Hospital, Edinburgh.
Scottish Medical Journal
|October 1, 1989
Abstract:
We describe the clinical features and post mortem findings in a patient with POEMS syndrome (P--polyneuropathy, O--organomegaly, E--endocrinopathy, M--M protein, S--skin changes), with particular emphasis on the evolution of the endocrinopathy over a three year period. In addition to gynaecomastia this case exhibited primary hypothyroidism and primary and secondary adrenal and gonadal failure. The widespread nature of the endocrine changes suggests that a circulating substance interferes with the action of trophic hormones, possibly by inhibiting second messenger production.