Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Search research articles

Related Experiment Videos

The Schöpf-Schulz-Passarge syndrome

P Verplancke¹, L Driessen, P Wynants

¹Department of Dermatology, University Hospital Gent, Belgium.

Dermatology (Basel, Switzerland)

|July 21, 1998

Summary

Schöpf-Schulz-Passarge syndrome, a rare genodermatosis, presents with skin and nail abnormalities. This case highlights a new association with poroma, a type of skin tumor, expanding our understanding of the syndrome.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by

Same author

[Pharmacobezoar in a woman with a clomipramine intoxication].

Nederlands tijdschrift voor geneeskunde·2021

Same author

Circulating APRIL levels are correlated with advanced disease and prognosis in rectal cancer patients.

Oncogenesis·2015

Same author

Dysplastic naevi, again.

Histopathology·2010

Same author

Coralline hydroxyapatite is a suitable bone graft substitute in an intra-articular goat defect model.

Journal of biomedical materials research. Part B, Applied biomaterials·2008

Same author

Extended cooperation in clinical studies through exchange of CDISC metadata between different study software solutions.

Methods of information in medicine·2006

Same author

Recommendations for the use of etanercept in psoriasis: a European dermatology expert group consensus.

Journal of the European Academy of Dermatology and Venereology : JEADV·2006

Area of Science:

Dermatology
Genetics
Oncology

Background:

Schöpf-Schulz-Passarge syndrome is a rare autosomal recessive genodermatosis.
It manifests with palmoplantar keratoderma, eyelid tumors, hypodontia, hypotrichosis, and nail hypoplasia.
Epithelial tumors have been previously reported in patients with this syndrome.

Observation:

This report details a unique case of Schöpf-Schulz-Passarge syndrome.
The patient presented with actinic keratoses, two tumors of the follicular infundibulum, and a poroma.
The poroma exhibited follicular differentiation.

Findings:

This case represents the first documented instance of Schöpf-Schulz-Passarge syndrome associated with a poroma.
The poroma demonstrated specific follicular differentiation.

Implications:

This finding expands the spectrum of epithelial tumors associated with Schöpf-Schulz-Passarge syndrome.
Further research may elucidate the specific oncogenic pathways involved in this genodermatosis.
Understanding these associations can improve diagnostic and management strategies for affected individuals.

Related Experiment Videos