Volume 11, Issue 1 pp. 59-65

Scleromyxoedema and thrombotic thrombocytopaenic purpura: two rare conditions both responding to plasma exchange

Karen E. Harman

Corresponding Author

Karen E. Harman

St. John's Institute of Dermatology, St. Thomas' Hospital, Lambeth Palace Road, London SE1 7EH, UK

*Corresponding author. Tel.: +44 171 9289292/3876; fax: +44 171 9228232; e-mail: [email protected]Search for more papers by this author
Ian C. Abbs

Ian C. Abbs

Guy's Hospital Renal Unit, Guy's Tower, St. Thomas' Street, London SE1 9RT, UK

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John M. Mahood

John M. Mahood

Northampton General Hospital, Cliftonville, Northampton NN1 5BD, UK

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Martin M. Black

Martin M. Black

St. John's Institute of Dermatology, St. Thomas' Hospital, Lambeth Palace Road, London SE1 7EH, UK

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First published: 29 September 2006
Citations: 5

Abstract

We report the case of a 66-year-old female who over an 18-month period developed severe, disabling scleromyxoedema with pulmonary fibrosis. Treatment with oral prednisolone and melphalan had failed to prevent disease progression. Treatment with a 5-day course of plasma exchange, intravenous cyclophosphamide (500 mg) and methyl-prednisolone (1 g on 3 consecutive days) was unfortunately followed by the development of thrombotic thrombocytopaenic purpura (TTP). After 17 extra plasma exchanges, she recovered and there has been a dramatic improvement in her skin signs. We postulate that the extra plasma exchanges which she received as a consequence of developing TTP have contributed to this result. To our knowledge, TTP has never been associated with scleromyxoedema, but it is likely to be a coincidence in this case.

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