Appelhans Carolin, Breuckmann Frank, Bastian Andreas, Altmeyer Peter, Kreuter Alexander
Dept, of Dermatology, Ruhr-University Bochum, Gudrunstr, 56, D-44791 Bochum, Germany.
BMC Dermatol. 2004 Nov 8;4(1):17. doi: 10.1186/1471-5945-4-17.
EMO syndrome, defined as a triad including exophthalmus, pretibial myxedema and osteoarthropathia, is a rare condition in patients suffering from hyperthyreosis.
We here describe an interesting case of EMO syndrome associated with unilateral fibromatosis of the hand and an initial stage of generalized myxedema of the skin. To our knowledge a similar case has not yet been described in literature though reports about associated fibromatosis, e.g. located retroperitoneally, already exist. Familiar explanations include its initiation by autoimmune processes or aberrant T-cell cytokine stimulation leading to an overwhelming production of glycosaminoglycans.
Interpreting our case in context with previous reports we conclude that associated fibromatosis induced by autoimmune processes may affect a variety of different localizations and therefore requires careful monitoring. A therapeutical attempt by using UVA1 irridation for pretibial myxedema remained without a satisfying regression.