[Giant papillomas of the tongue and pharynx in focal dermal hypoplasia: a case report].

Standard

[Giant papillomas of the tongue and pharynx in focal dermal hypoplasia: a case report]. / Kornek, Thomas; Augustin, Matthias; Krause, K; Teudt, I U; Neuber, K; Herberger, Katharina.

in: HAUTARZT, Jahrgang 63, Nr. 1, 1, 2012, S. 39-41.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

APA

Vancouver

Bibtex

@article{55aeb329c1c1412489a6d9ba238959a8,
title = "[Giant papillomas of the tongue and pharynx in focal dermal hypoplasia: a case report].",
abstract = "Focal dermal hypoplasia is a rare congenital syndrome with dominant X-linked mode of inheritance characterized by a wide range of meso-ectodermal anomalies. The clinical variation is great, as explained by the Lyon hypothesis and mosaicism. Findings include skin atrophy along the lines of Blaschko and papillomas. Our case is striking with rapidly-growing giant pharyngeal papillomas which caused dysphagia and required resection.",
keywords = "Diagnosis, Differential, Humans, Female, Young Adult, Treatment Outcome, Aphasia/etiology, Focal Dermal Hypoplasia/complications/*diagnosis/surgery, Papilloma/*diagnosis/surgery, Pharyngeal Neoplasms/*diagnosis/surgery, Tongue Neoplasms/*diagnosis/surgery, Diagnosis, Differential, Humans, Female, Young Adult, Treatment Outcome, Aphasia/etiology, Focal Dermal Hypoplasia/complications/*diagnosis/surgery, Papilloma/*diagnosis/surgery, Pharyngeal Neoplasms/*diagnosis/surgery, Tongue Neoplasms/*diagnosis/surgery",
author = "Thomas Kornek and Matthias Augustin and K Krause and Teudt, {I U} and K Neuber and Katharina Herberger",
year = "2012",
language = "Deutsch",
volume = "63",
pages = "39--41",
journal = "HAUTARZT",
issn = "0017-8470",
publisher = "Springer",
number = "1",

}

RIS

TY - JOUR

T1 - [Giant papillomas of the tongue and pharynx in focal dermal hypoplasia: a case report].

AU - Kornek, Thomas

AU - Augustin, Matthias

AU - Krause, K

AU - Teudt, I U

AU - Neuber, K

AU - Herberger, Katharina

PY - 2012

Y1 - 2012

N2 - Focal dermal hypoplasia is a rare congenital syndrome with dominant X-linked mode of inheritance characterized by a wide range of meso-ectodermal anomalies. The clinical variation is great, as explained by the Lyon hypothesis and mosaicism. Findings include skin atrophy along the lines of Blaschko and papillomas. Our case is striking with rapidly-growing giant pharyngeal papillomas which caused dysphagia and required resection.

AB - Focal dermal hypoplasia is a rare congenital syndrome with dominant X-linked mode of inheritance characterized by a wide range of meso-ectodermal anomalies. The clinical variation is great, as explained by the Lyon hypothesis and mosaicism. Findings include skin atrophy along the lines of Blaschko and papillomas. Our case is striking with rapidly-growing giant pharyngeal papillomas which caused dysphagia and required resection.

KW - Diagnosis, Differential

KW - Humans

KW - Female

KW - Young Adult

KW - Treatment Outcome

KW - Aphasia/etiology

KW - Focal Dermal Hypoplasia/complications/diagnosis/surgery

KW - Papilloma/diagnosis/surgery

KW - Pharyngeal Neoplasms/diagnosis/surgery

KW - Tongue Neoplasms/diagnosis/surgery

KW - Diagnosis, Differential

KW - Humans

KW - Female

KW - Young Adult

KW - Treatment Outcome

KW - Aphasia/etiology

KW - Focal Dermal Hypoplasia/complications/diagnosis/surgery

KW - Papilloma/diagnosis/surgery

KW - Pharyngeal Neoplasms/diagnosis/surgery

KW - Tongue Neoplasms/diagnosis/surgery

M3 - SCORING: Zeitschriftenaufsatz

VL - 63

SP - 39

EP - 41

JO - HAUTARZT

JF - HAUTARZT

SN - 0017-8470

IS - 1

M1 - 1

ER -