Clinical, morphogical and immunohistochemical aspects of oral inflammatory myofibroblastic tumor: a rare case report in a pediatric patient

Authors

  • Hellen Bandeira de Pontes Santos
  • Natália Guimarães Barbosa
  • Tiago João Silva Filho
  • Lélia Maria Guedes Queiroz
  • Alberto Gurgel
  • Roseana de Almeida Freitas
  • Patrícia Teixeira de Oliveira

DOI:

https://doi.org/10.21270/archi.v7i10.3088

Abstract

Inflammatory myofibroblastic tumor (IMT) is a rare benign neoplasm composed by myofibroblasts and fibroblasts admixed with inflammatory cells. Here, we report a case of IMT in the oral cavity of left mandible of a 12-year-old boy. Histopathological investigation revealed a proliferation of fibroblasts and myofibroblasts (positive for alpha-smooth muscle actin and vimentin) associated with inflammatory cells. The patient is still under follow-up and without evidence of recurrence. Oral IMT is a challenge for the clinician in diagnosis due to the nonspecific clinical presentation. Thus, histology and immunohistochemistry are required to reach an accurate diagnosis of this lesion.

Descriptors: Neoplasms; Diagnosis; Immunohistochemistry.

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References

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Published

2018-12-13

How to Cite

Santos, H. B. de P., Barbosa, N. G., Silva Filho, T. J., Queiroz, L. M. G., Gurgel, A., Freitas, R. de A., & Oliveira, P. T. de. (2018). Clinical, morphogical and immunohistochemical aspects of oral inflammatory myofibroblastic tumor: a rare case report in a pediatric patient. ARCHIVES OF HEALTH INVESTIGATION, 7(10). https://doi.org/10.21270/archi.v7i10.3088

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Section

Relatos de Caso