Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich

Standard

Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich. / Friedrich, R E; Gehrke, G; Giese, M; Mautner, V F; Schmelzle, R.

in: Mund Kiefer Gesichtschir, Jahrgang 2 Suppl 1, 01.05.1998, S. S86-90.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Friedrich, RE, Gehrke, G, Giese, M, Mautner, VF & Schmelzle, R 1998, 'Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich', Mund Kiefer Gesichtschir, Jg. 2 Suppl 1, S. S86-90.

APA

Friedrich, R. E., Gehrke, G., Giese, M., Mautner, V. F., & Schmelzle, R. (1998). Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich. Mund Kiefer Gesichtschir, 2 Suppl 1, S86-90.

Vancouver

Friedrich RE, Gehrke G, Giese M, Mautner VF, Schmelzle R. Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich. Mund Kiefer Gesichtschir. 1998 Mai 1;2 Suppl 1:S86-90.

Bibtex

@article{c8514ba4af364d95be234d7c3476e4d4,
title = "Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich",
abstract = "Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary disease of high penetrance and variable expression. Epidemiologic data on craniofacial manifestations are still lacking. Up until now 74 patients with NF1 have been treated at the Department of Oral and Maxillofacial Surgery of the University of Hamburg. Forty-two patients presented periorbital and orbital neurofibromas varying in extension and in the severity of findings of the affected site. Surgical therapy is mainly based on tumour reduction, frequently combined with face-lifting. In our experience neurofibromas of the neck tend to be pseudo-encapsulated, facilitating the preparation of the tumour. On the other hand, identification and preparation of diffuse infiltrating neurofibromas in the trigeminal nerve region are difficult and local recurrence must be expected.",
keywords = "Adult, Child, Preschool, Craniotomy, Female, Follow-Up Studies, Head and Neck Neoplasms, Humans, Male, Neurofibroma, Plexiform, Neurofibromatosis 1, Orbital Neoplasms, Reoperation, Rhytidoplasty, Treatment Outcome",
author = "Friedrich, {R E} and G Gehrke and M Giese and Mautner, {V F} and R Schmelzle",
year = "1998",
month = may,
day = "1",
language = "Deutsch",
volume = "2 Suppl 1",
pages = "S86--90",

}

RIS

TY - JOUR

T1 - Tumorreduktion plexiformer Neurofibrome im kraniofazialen und Halsbereich

AU - Friedrich, R E

AU - Gehrke, G

AU - Giese, M

AU - Mautner, V F

AU - Schmelzle, R

PY - 1998/5/1

Y1 - 1998/5/1

N2 - Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary disease of high penetrance and variable expression. Epidemiologic data on craniofacial manifestations are still lacking. Up until now 74 patients with NF1 have been treated at the Department of Oral and Maxillofacial Surgery of the University of Hamburg. Forty-two patients presented periorbital and orbital neurofibromas varying in extension and in the severity of findings of the affected site. Surgical therapy is mainly based on tumour reduction, frequently combined with face-lifting. In our experience neurofibromas of the neck tend to be pseudo-encapsulated, facilitating the preparation of the tumour. On the other hand, identification and preparation of diffuse infiltrating neurofibromas in the trigeminal nerve region are difficult and local recurrence must be expected.

AB - Neurofibromatosis type 1 (NF1) is an autosomal dominant hereditary disease of high penetrance and variable expression. Epidemiologic data on craniofacial manifestations are still lacking. Up until now 74 patients with NF1 have been treated at the Department of Oral and Maxillofacial Surgery of the University of Hamburg. Forty-two patients presented periorbital and orbital neurofibromas varying in extension and in the severity of findings of the affected site. Surgical therapy is mainly based on tumour reduction, frequently combined with face-lifting. In our experience neurofibromas of the neck tend to be pseudo-encapsulated, facilitating the preparation of the tumour. On the other hand, identification and preparation of diffuse infiltrating neurofibromas in the trigeminal nerve region are difficult and local recurrence must be expected.

KW - Adult

KW - Child, Preschool

KW - Craniotomy

KW - Female

KW - Follow-Up Studies

KW - Head and Neck Neoplasms

KW - Humans

KW - Male

KW - Neurofibroma, Plexiform

KW - Neurofibromatosis 1

KW - Orbital Neoplasms

KW - Reoperation

KW - Rhytidoplasty

KW - Treatment Outcome

M3 - SCORING: Zeitschriftenaufsatz

C2 - 9658829

VL - 2 Suppl 1

SP - S86-90

ER -