Background: Inflammatory myofibroblastic tumor (IMT) is a neoplasm of unknown etiology occurring at various sites. By definition, it is composed of spindle cells (myofibroblasts) with variable inflammatory component, hence the name is IMT.
Case Presentation: The present case is of a 46 years old woman presented with a history of flank pain, abdominal mass and intermittent hematuria for last 6 months. The initial diagnosis was kept as renal cell carcinoma. Finally, it turned out to be a case of retroperitoneal IMT. The patient was managed by complete surgical resection of the tumor.
Conclusion: IMT is a rare neoplasm of uncertain biological potential. Complete surgical resection remains the mainstay of the treatment.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1276822 | PMC |
| http://dx.doi.org/10.1186/1477-7819-3-66 | DOI Listing |
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