| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8807163 | Annals of Diagnostic Pathology | 2018 | 4 Pages |
Abstract
In conclusion, multifocal desmoid tumors are a very rare disease and may occur in sporadic cases that are characterized by recurrent CTNNB1 mutations. However, the underlying pathogenesis of multifocal desmoid tumors remains poorly understood with often aggressive clinical behavior and challenging therapeutical management.
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Authors
Elise M. Bekers, Danique L.M. van Broekhoven, Thijs van Dalen, Johan J. Bonenkamp, Ingrid C.M. van der Geest, Jacky W.J. de Rooy, Joost M. van Gorp, David H. Creytens, Wendy W.J. de Leng, Blanca Scheijen, Astrid Eijkelenboom, Uta Flucke,