Presence ofC11orf95-MKL2fusion is a consistent finding in chondroid lipomas: a study of eight cases

Author:

Flucke Uta1,Tops Bastiaan B J1,de Saint Aubain Somerhausen Nicolas2,Bras Johannes3,Creytens David H4,Küsters Benno1,Groenen Patricia J T A1,Verdijk Marian A J1,Suurmeijer Albert J H5,Mentzel Thomas6

Affiliation:

1. Department of Pathology; Radboud University Nijmegen Medical Centre; Nijmegen; The Netherlands

2. Jules Bordet Institute; Brussels; Belgium

3. Department of Pathology; Academic Medical Center; Amsterdam; The Netherlands

4. Department of Pathology; Ghent University Hospital; Ghent; Belgium

5. Department of Pathology and Medical Biology; University Medical Centre Groningen; Groningen; The Netherlands

6. Dermatopathologie Bodensee; Friedrichshafen; Germany

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Reference30 articles.

1. Chondroid lipoma. A unique tumor simulating liposarcoma and myxoid chondrosarcoma;Meis;Am. J. Surg. Pathol.,1993

2. Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics;Gisselson;Am. J. Surg. Pathol.,1999

3. Cytogenetic and cytologic features of chondroid lipoma of soft tissue;Thomson;Mod. Pathol.,1999

4. Chondroid lipoma is characterized by t(11;16)(q13;p12-13);Ballaux;Virchows Arch.,2004

5. C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma;Huang;Genes Chromosom. Cancer,2010

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