AI Article Synopsis

  • Inflammatory myofibroblastic tumors (IMTs) can have both neoplastic and nonneoplastic characteristics and can occur anywhere in the body, but certain sites like the nasal cavity exhibit more aggressive behavior.
  • A case study of a 34-year-old female with a resistant IMT in the maxillary sinus shows that her tumor did not respond to current therapies, highlighting the complexity of treating IMTs.
  • The paper emphasizes the need for understanding the genetic variations within IMTs to develop more effective targeted treatments and includes a literature review of IMTs in the maxillary sinus from 1985 to 2014.

Article Abstract

An inflammatory myofibroblastic tumor (IMT) is an immunohistochemically diverse entity demonstrating neoplastic and nonneoplastic qualities. Although IMTs can arise in any area of the body, lesions arising in certain sites, namely, the nasal cavity, paranasal sinuses, and pterygopalatine fossa, demonstrate a heightened neoplastic and invasive potential. Despite case specific complete tumor regression and disease remission in response to pharmacotherapeutics, a subset of IMTs remain resistant to all forms of therapy. We present such a case, a 34-year-old female patient, with a highly resistant, maxillary sinus IMT. Her refractory, ALK-1 negative IMT has not responded well to novel therapies reported in current literature. This case suggests the role of zonal expressivity within a single lesion as a probable mechanism for its highly resistant nature and should promote determination of each IMT's cytogenetic profile to provide more effective targeted therapy. Paper includes a literature review of all maxillary sinus IMTs from 1985 to 2014 along with their immunohistochemical staining, treatments, and outcomes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339865PMC
http://dx.doi.org/10.1155/2015/953857DOI Listing

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