Familial lichen sclerosus et atrophicus in association with CREST syndrome: a case report

Summary Lichen sclerosus et atrophicus is an uncommon disease which appears to be multifaetorial in aetiology. We describe a case of a young woman with CREST syndrome (calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly and telangiectasial who has a documented family histor...

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Veröffentlicht in:British journal of dermatology (1951) 1996-06, Vol.134 (6), p.1144-1146
Hauptverfasser: FITZGERALD, E.A., CONNELLY, C.S., PURCELL, S.M., KANTOR, G.R.
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Sprache:eng
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Zusammenfassung:Summary Lichen sclerosus et atrophicus is an uncommon disease which appears to be multifaetorial in aetiology. We describe a case of a young woman with CREST syndrome (calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly and telangiectasial who has a documented family history of two sisters with lichen sclerosus et atrophicus. She presented with vulvar pruritas in association with dyspareunia. and biopsy of atrophic white vulvar lesions was consistent with lichen sclerosus et atrophicus. Lichen sclerosus et atrophicus has been previously noted to occur in association with morphoea and lichen planus, although it has never been reported in conjunction with CREST syndrome.
ISSN:0007-0963
1365-2133
DOI:10.1046/j.1365-2133.1996.d01-921.x