Literature DB >> 31490237

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

Fernanda Amary1,2, Eva Markert1, Fitim Berisha1, Hongtao Ye1, Craig Gerrand1, Paul Cool3, Roberto Tirabosco1, Daniel Lindsay1, Nischalan Pillay1,2, Paul O'Donnell1, Daniel Baumhoer4, Adrienne M Flanagan1,2.   

Abstract

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.

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Year:  2019        PMID: 31490237     DOI: 10.1097/PAS.0000000000001355

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  7 in total

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2.  GRM1 Immunohistochemistry Distinguishes Chondromyxoid Fibroma From its Histologic Mimics.

Authors:  Angus M S Toland; Suk Wai Lam; Sushama Varma; Aihui Wang; Brooke E Howitt; Christian A Kunder; Darcy A Kerr; Karoly Szuhai; Judith V M G Bovée; Gregory W Charville
Journal:  Am J Surg Pathol       Date:  2022-06-01       Impact factor: 6.298

3.  Clinicopathologic and molecular features of vascular tumors in a series of 118 cases.

Authors:  Huiting Wei; Tiantian Zhen; Ying Tuo; Hui Li; Jiangtao Liang; Shaoyu Chen; Huijuan Shi; Anjia Han
Journal:  Am J Transl Res       Date:  2022-05-15       Impact factor: 3.940

4.  Extraosseous osteoblastoma: A rare cause of breast mass in a prepubertal girl.

Authors:  Sabine Danzinger; Leo Kager; Maria Bernathova; Susanna Lang; Werner Haslik; Christian F Singer
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Review 5.  Diagnostic Immunohistochemistry of Soft Tissue and Bone Tumors: An Update on Biomarkers That Correlate with Molecular Alterations.

Authors:  William J Anderson; Vickie Y Jo
Journal:  Diagnostics (Basel)       Date:  2021-04-12

6.  Methylation and copy number profiling: emerging tools to differentiate osteoblastoma from malignant mimics?

Authors:  Baptiste Ameline; Michaela Nathrath; Karolin H Nord; Felix Haglund de Flon; Judith V M G Bovée; Andreas H Krieg; Sylvia Höller; Jürgen Hench; Daniel Baumhoer
Journal:  Mod Pathol       Date:  2022-03-28       Impact factor: 8.209

7.  Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma.

Authors:  Karim H Saba; Louise Cornmark; Jakob Hofvander; Linda Magnusson; Jenny Nilsson; Hilda van den Bos; Diana Cj Spierings; Floris Foijer; Johan Staaf; Otte Brosjö; Vaiyapuri P Sumathi; Suk Wai Lam; Karoly Szuhai; Judith Vmg Bovée; Michal Kovac; Daniel Baumhoer; Emelie Styring; Karolin H Nord
Journal:  J Pathol Clin Res       Date:  2020-06-16
  7 in total

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