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Published in: European Journal of Medical Research 6/2009

01-12-2009 | Review

Chest wall and intrathoracic desmoid tumors: surgical experience and review of the literature

Authors: E Bölke, H Krasniqi, G Lammering, R Engers, C Matuschek, S Gripp, PA Gerber, G Fischer, M Peiper, S Shaikh, W Budach, K Orth

Published in: European Journal of Medical Research | Issue 6/2009

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Abstract

Desmoid tumors are fibroblastic/myofibroblastic neoplasms, which originate from musculo-aponeurotic structures and are classified as deep fibromatoses. Despite their benign histologic appearance and lack of metastatic potential, desmoid tumors may cause aggressive local infiltrations and compression of surrounding structures. They are often associated with female gender, familial adenomatous polyposis (FAP) and sporadically may occur at sites of previous trauma, scars or irradiation. Molecular studies have demonstrated that these patients are associated with a bi-allelic APC mutation in the affected tissue. Radical tumor resection with free margins remains the first therapy of choice. In cases with anatomical or technical limitations for a wide excision, radiation therapy represents a proven and effective alternative or supplementary treatment.
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Metadata
Title
Chest wall and intrathoracic desmoid tumors: surgical experience and review of the literature
Authors
E Bölke
H Krasniqi
G Lammering
R Engers
C Matuschek
S Gripp
PA Gerber
G Fischer
M Peiper
S Shaikh
W Budach
K Orth
Publication date
01-12-2009
Publisher
BioMed Central
Published in
European Journal of Medical Research / Issue 6/2009
Electronic ISSN: 2047-783X
DOI
https://doi.org/10.1186/2047-783X-14-6-240

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