| Literature DB >> 18805200 |
Alicia Privette1, Peter Fisk, Bruce Leavitt, Kumarasen Cooper, Laurence McCahill.
Abstract
Inflammatory myofibroblastic tumor is a rare neoplasm of intermediate malignant potential. Although inflammatory myofibroblastic tumor occurs at multiple anatomic locations, an esophageal lesion is extremely rare. We describe a 43-year-old man who presented with severe dysphagia and an inflammatory syndrome, secondary to esophageal inflammatory myofibroblastic tumor. The patient was treated successfully with esophagectomy and remains disease free at 1 year. This case illustrates the complexities involved in managing a large esophageal myofibroblastic tumor and highlights that esophagectomy, rather than enucleation, should be the treatment of choice.Entities:
Mesh:
Year: 2008 PMID: 18805200 DOI: 10.1016/j.athoracsur.2008.03.056
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330