Abstract
Background and Case Presentation: A patient with nevoid basal cell carcinoma syndrome (Gorlin syndrome) presented with two unusual clinical features, i.e. adenocarcinoma of the small bowel and extensive mesenchymal proliferation of the lower gastrointestinal tract. Conclusions: We discuss the possibility that these two features are pathogenetically linked to the formerly undescribed patient's PTCH germ line mutation.
Dokumententyp: | Zeitschriftenartikel |
---|---|
Publikationsform: | Publisher's Version |
Fakultät: | Medizin |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
URN: | urn:nbn:de:bvb:19-epub-23238-6 |
ISSN: | 1471-2407 |
Sprache: | Englisch |
Dokumenten ID: | 23238 |
Datum der Veröffentlichung auf Open Access LMU: | 05. Mrz. 2015, 09:34 |
Letzte Änderungen: | 04. Nov. 2020, 13:04 |