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Fibromatosis of the hand associated with EMO syndrome: a case report
Carolin Appelhans1, Frank Breuckmann, Andreas Bastian
1Dept, of Dermatology, Ruhr-University Bochum, Gudrunstr, 56, D-44791 Bochum, Germany. Carolin.Appelhans@ruhr-uni-bochum.de
Background:
EMO syndrome, defined as a triad including exophthalmus, pretibial myxedema and osteoarthropathia, is a rare condition in patients suffering from hyperthyreosis.
Case Presentation:
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.
Conclusion:
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.