| A case of Schöpf-Schulz-Passarge syndrome. | |
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MedLine Citation:
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PMID: 16045686 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Schöpf-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. |
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Authors:
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P J Hampton; B Angus; A J Carmichael |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Clinical and experimental dermatology Volume: 30 ISSN: 0307-6938 ISO Abbreviation: Clin. Exp. Dermatol. Publication Date: 2005 Sep |
Date Detail:
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Created Date: 2005-07-27 Completed Date: 2005-11-21 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 7606847 Medline TA: Clin Exp Dermatol Country: England |
Other Details:
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Languages: eng Pagination: 528-30 Citation Subset: IM |
Affiliation:
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Pathology, Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne, UK. hamptonpj@doctors.org.uk |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Aged Cysts / pathology Ectodermal Dysplasia / pathology* Eyelid Diseases / pathology Hidrocystoma / pathology Humans Hypotrichosis / pathology Keratoderma, Palmoplantar / pathology* Male Nail Diseases / pathology Sweat Gland Neoplasms / pathology Syndrome |
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