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Lookup NU author(s): Dr Brian Angus,
Dr Andrew Carmichael
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Schopf-Schulz-Passarge syndrome (SSPS) is a rare ectodermal dysplasia characterized by hypodontia, hypotrichosis, nail dystrophy, palmoplantar keratoderma, and periocular and eyelid margin apocrine hidrocystomas. Several other skin tumours have been described in association with this syndrome, in particular, multiple palmoplantar eccrine syringofibroadenoma (ESFA). We report a case of SSPS with diffuse palmoplantar hyperkeratosis, which was shown by histology and immunocytochemistry to be due to ESFA.
Author(s): Hampton PJ, Angus B, Carmichael AJ
Publication type: Article
Publication status: Published
Journal: Clinical and Experimental Dermatology
ISSN (print): 0307-6938
ISSN (electronic): 1365-2230
Publisher: Blackwell Publishing Ltd
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