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   <subfield code="a">Scleroderma-like syndrome in a child: eosinophilic fasciitis or scleredema adultorum?</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Martina Huemer, Arno Seeber, Christian Huemer]</subfield>
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   <subfield code="a">A 6-year-old female patient presented with a rapidly progressive scleroderma-like syndrome involving almost the entire integument. Initially clinical patterns and histopathological data of both eosinophilic fasciitis and scleredema adultorum were present. The course of the disease remained unusual for both conditions but finally argued in favour of the diagnosis of eosinophilic fasciitis. Conclusion Eosinophilic fasciitis and scleredema adultorum might be subtypes of one disease entity.</subfield>
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   <subfield code="a">Key words Scleroderma-like syndrome</subfield>
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   <subfield code="a">Scleredema adultorum</subfield>
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   <subfield code="u">Department of Paediatrics, University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria e-mail: martina.huemer@akh-wien.ac.at Tel.: +43-1-404003154; Fax: +43-1-404003154, AT</subfield>
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