Literature DB >> 16045686

A case of Schöpf-Schulz-Passarge syndrome.

P J Hampton1, B Angus, A J Carmichael.   

Abstract

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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Year:  2005        PMID： 16045686     DOI： 10.1111/j.1365-2230.2005.01855.x

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN： 0307-6938            Impact factor:   3.470


  4 in total

1.  Bilateral multiple axillary apocrine hidrocystomas associated with benign apocrine hyperplasia.

Authors:  N A Obaidat; D M Ghazarian
Journal:  J Clin Pathol       Date:  2006-07       Impact factor: 3.411

2.  Histological study of eyelid hidrocystoma: A clinical case.

Authors:  Sofia Karachrysafi; Georgios Fadel; Viktoria Kapourani; Fani Akritidou; Pinelopi Anastasiadou; Theodora Papamitsou; Antonia Sioga; Elie Fadel
Journal:  SAGE Open Med Case Rep       Date:  2022-05-11

3.  Schopf-Schulz-Passarge Syndrome.

Authors:  Kinjal D Rambhia; Vidya Kharkar; Sunanda Mahajan; Uday S Khopkar
Journal:  Indian Dermatol Online J       Date:  2018 Nov-Dec

4.  Reactive Eccrine Syringofibroadenoma Associated with Neuropathy, Venous Stasis, and Diabetic Foot Ulcer.

Authors:  Thirawut Sirikham; Salinee Rojhirunsakool; Vasanop Vachiramon
Journal:  Case Rep Dermatol       Date:  2016-06-02
  4 in total

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