Eccrine syringofibroadenoma as a clue for the diagnosis of Schöpf‐Schulz‐Passarge syndrome in acquired palmoplantar keratoderma-Reference-Cited by-同舟云学术

Eccrine syringofibroadenoma as a clue for the diagnosis of Schöpf‐Schulz‐Passarge syndrome in acquired palmoplantar keratoderma

Published:2020-06 Issue:10 Volume:47 Page:987-989
ISSN:0303-6987
Container-title:Journal of Cutaneous Pathology
language:en
Short-container-title:J Cutan Pathol

Author:

Riera‐Monroig Josep¹^ORCID,Martínez‐Romero María del Carmen²,Alós Llucia³,Guillén‐Navarro Encarnación⁴,Mascaró José‐Manuel¹

Affiliation:

1. Department of Dermatology, Hospital Clínic University of Barcelona Barcelona Spain

2. Molecular Genetics Section, Centro de Bioquímica y Genética Clínica Hospital Clínico Universitario Virgen de la Arrixaca, IMIB‐Arrixaca, Programa de Doctorado Ciencias de la Salud‐UCAM, CIBERER‐ISCIII Murcia Spain

3. Department of Pathology, Hospital Clínic University of Barcelona Barcelona Spain

4. Medical Genetics Section, Department of Pediatrics Hospital Clínico Universitario Virgen de la Arrixaca, IMIB‐Arrixaca, Universidad de Murcia, CIBERER‐ISCIII Murcia Spain

Publisher

Wiley

Subject

Dermatology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cup.13743

Reference10 articles.

1. Clinical features and WNT 10A mutations in seven unrelated cases of Schöpf–Schulz–Passarge syndrome

2. Considérations sur les tumeurs fibro‐épitheliales: Le syringofibroadenome eccrine;Mascaro JM;Ann Dermatol Syphilgr,1963

3. Eccrine syringofibroadenoma: Multiple lesions representing a new cutaneous marker of the Schöpf syndrome, and solitary nonhereditary tumors

4. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population

5. Clouston Syndrome and Eccrine Syringofibroadenomas

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