Plexiform fibrohistiocytic tumor: a clinicopathological and immunohistochemical study of 39 tumors, with evidence for a CSF1-producing “null cell” population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00428-022-03408-2.pdf
Reference37 articles.
1. Enzinger FM, Zhang R (1988) Plexiform fibrohistiocytic tumor presenting in children and young adults An analysis of 65 cases. Ame J Surg Pathol 12:818–826
2. (2020) Soft tissue and bone tumours. International Agency for Research on Cancer, Lyon, France
3. Moosavi C, Jha P, Fanburg-Smith JC (2007) An update on plexiform fibrohistiocytic tumor and addition of 66 new cases from the Armed Forces Institute of Pathology, in honor of Franz M. Enzinger, MD Annals of diagnostic pathology 11:313–319
4. Jaffer S, Ambrosini-Spaltro A, Mancini AM, Eusebi V, Rosai J (2009) Neurothekeoma and plexiform fibrohistiocytic tumor: mere histologic resemblance or histogenetic relationship? Am J Surg Pathol 33:905–913. https://doi.org/10.1097/PAS.0b013e31819c79f7
5. Papke DJ Jr, Al-Ibraheemi A, Fletcher CDM (2020) Plexiform myofibroblastoma: clinicopathologic analysis of 36 cases of a distinctive benign tumor of soft tissue affecting mainly children and young adults. Am J Surg Pathol 44:1469–1478. https://doi.org/10.1097/PAS.0000000000001534
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