Volume 64, Issue 5 pp. 639-646
Original Article

BRAF mutation in ‘sarcomas’: a possible method to detect de-differentiated melanomas

Nicole A Cipriani

Corresponding Author

Nicole A Cipriani

Department of Pathology, The University of Chicago, Chicago, IL, USA

The majority of this work was performed at Massachusetts General Hospital, Boston, MA, USA.Address for correspondence: N A Cipriani MD, The University of Chicago Medicine, 5841 S. Maryland Ave., MC 6101, Chicago, IL 60637, USA. e-mail: [email protected]Search for more papers by this author
Igor Letovanec

Igor Letovanec

Institut Universitaire de Pathologie, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland

Search for more papers by this author
Francis J Hornicek

Francis J Hornicek

Center for Sarcoma and Connective Tissue Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

Search for more papers by this author
John T Mullen

John T Mullen

Division of Surgical Oncology, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

Search for more papers by this author
Zhenfeng Duan

Zhenfeng Duan

Center for Sarcoma and Connective Tissue Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

Search for more papers by this author
Darrell R Borger

Darrell R Borger

Division of Hematology-Oncology and Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

These authors are co-last authors.Search for more papers by this author
Gunnlaugur Petur Nielsen

Gunnlaugur Petur Nielsen

Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

These authors are co-last authors.Search for more papers by this author
First published: 05 October 2013
Citations: 34

Abstract

Aims

BRAF is mutated in 50–60% of melanomas, but BRAF mutation in sarcomas has not been systematically evaluated. Some melanomas are spindled and may show no immunohistochemical evidence of melanocytic differentiation. Similarly, many sarcomas are undifferentiated, i.e. undifferentiated pleomorphic sarcomas (UPS). Diagnosing melanoma versus sarcoma in an undifferentiated spindle cell malignancy can be challenging. Our aim was to evaluate the prevalence of BRAF mutation in sarcomas and the use of BRAF mutational status in the diagnosis of spindle cell malignancies.

Methods and results

BRAF mutational analysis was performed on tissue from 104 patients: 90 with sarcoma only (50 UPS) and 14 with sarcoma and melanoma (seven UPS). In the sarcoma-only group, BRAF mutation was absent. In the sarcoma–melanoma group, three sarcomas showed BRAF mutation; all were UPS, occurred after the melanomas and did not stain for melanocytic markers. One melanoma–sarcoma pair showed identical BRAF V600E mutations.

Conclusions

The presence of BRAF mutation in these tumours raises the possibility that poorly differentiated spindle cell malignancies with BRAF mutation may represent melanomas, and BRAF mutational analysis should be considered in a patient with a spindle cell malignancy and a history of melanoma, as a positive result may indicate de-differentiated melanoma.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.