FOS Expression in Osteoid Osteoma and Osteoblastoma: A Valuable Ancillary Diagnostic Tool.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
12 2019
Historique:
pubmed: 7 9 2019
medline: 14 4 2020
entrez: 7 9 2019
Statut: ppublish

Résumé

Osteoblastoma and osteoid osteoma together are the most frequent benign bone-forming tumor, arbitrarily separated by size. In some instances, it can be difficult to differentiate osteoblastoma from osteosarcoma. Following our recent description of FOS gene rearrangement in these tumors, the aim of this study is to evaluate the value of immunohistochemistry in osteoid osteoma, osteoblastoma, and osteosarcoma for diagnostic purposes. A total of 337 cases were tested with antibodies against c-FOS: 84 osteoblastomas, 33 osteoid osteomas, 215 osteosarcomas, and 5 samples of reactive new bone formation. In all, 83% of osteoblastomas and 73% of osteoid osteoma showed significant expression of c-FOS in the osteoblastic tumor cell component. Of the osteosarcomas, 14% showed c-FOS expression, usually focal, and in areas with severe morphologic atypia which were unequivocally malignant: 4% showed more conspicuous expression, but these were negative for FOS gene rearrangement. We conclude that c-FOS immunoreactivity is present in the vast majority of osteoblastoma/osteoid osteoma, whereas its expression is usually focal or patchy, in no more than 14% of osteosarcoma biopsies. Therefore, any bone-forming tumor cases with worrying histologic features would benefit from fluorescence in situ hybridization analysis for FOS gene rearrangement. Our findings highlight the importance of undertaking a thorough assessment of expression patterns of antibodies in the light of morphologic, clinical, and radiologic features.

Identifiants

pubmed: 31490237
doi: 10.1097/PAS.0000000000001355
doi:

Substances chimiques

Biomarkers, Tumor 0
FOS protein, human 0
Proto-Oncogene Proteins c-fos 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1661-1667

Auteurs

Fernanda Amary (F)

Royal National Orthopaedic Hospital, Stanmore.
Cancer Institute, University College London, London.

Eva Markert (E)

Royal National Orthopaedic Hospital, Stanmore.

Fitim Berisha (F)

Royal National Orthopaedic Hospital, Stanmore.

Hongtao Ye (H)

Royal National Orthopaedic Hospital, Stanmore.

Craig Gerrand (C)

Royal National Orthopaedic Hospital, Stanmore.

Paul Cool (P)

The Robert Jones and Agnes Hunt Orthopaedic Hospital, Oswestry and Keele University, Owestry, UK.

Roberto Tirabosco (R)

Royal National Orthopaedic Hospital, Stanmore.

Daniel Lindsay (D)

Royal National Orthopaedic Hospital, Stanmore.

Nischalan Pillay (N)

Royal National Orthopaedic Hospital, Stanmore.
Cancer Institute, University College London, London.

Paul O'Donnell (P)

Royal National Orthopaedic Hospital, Stanmore.

Daniel Baumhoer (D)

Basel Bone Tumour Reference Centre (BBTRC), University Hospital Basel and University of Basel, Basel, Switzerland.

Adrienne M Flanagan (AM)

Royal National Orthopaedic Hospital, Stanmore.
Cancer Institute, University College London, London.

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Classifications MeSH