Abstract:A 54-year-old man with a complaint of dysphagia was found to have a prominent stricture in the proximal esophagus. A biopsy of the stenotic area indicated sarcoma, leading to subtotal esophagectomy. The surgically removed esophagus demonstrated a well-defined intramural mass, consisting of a mixture of fibroblastic cells with bland cytological appearances and inflammatory cells. Reflux esophagitis which was present distal to the stricture seemed to play a role in the development of this inflammatory pseudotumo… Show more
“…IMT exhibits immunopositivity for vimentin, partly for desmin, actin, and cytokeratin and immunonegativity for S-100, CD34, CD117, and CD68. 1,7,8 The most commonly reported primary therapy is surgical resection (i.e., enucleation and partial or total esophagectomy). 7-10 The use of enucleation versus esophagectomy must be balanced between the recurrence risk and operative morbidity.…”
“…IMT exhibits immunopositivity for vimentin, partly for desmin, actin, and cytokeratin and immunonegativity for S-100, CD34, CD117, and CD68. 1,7,8 The most commonly reported primary therapy is surgical resection (i.e., enucleation and partial or total esophagectomy). 7-10 The use of enucleation versus esophagectomy must be balanced between the recurrence risk and operative morbidity.…”
“…8 In the gastrointestinal tract, the documented sites include esophagus, small intestine, colon, appendix, rectum, pancreases, spleen, liver, or a Meckel's diverticulum. [9][10][11] Especially in bilopancreati tract, most IMTs have been reported in pancreas 12,13 but the biliary IMT is even rarer. 14 Because pancreatic IMT was commonly mistaken for a pancreatic cancer clinically and radiologically, surgical resection was usually known as effective treatment.…”
Inflammatory myofibroblastic tumors (IMTs) are solid neoplastic mesenchymal proliferations composed of myofibroblastic spindle cells admixed with inflammatory infiltrates. The documented sites in the gastrointestinal tract include the esophagus, small intestine, colon, appendix, rectum, pancreas, spleen, liver, and Meckel's diverticulum. Biliary IMTs are rare, and IMTs arising from the ampulla of Vater have not been reported previously. Herein we report the case of a 65-year-old woman with an extrahepatic biliary obstruction due to IMT of the ampulla of Vater, and a successful therapeutic approach using endoscopic ultrasonography and endoscopic papillectomy. (Gut Liver 2010;4: 419-422)
“…Recurrence after complete resection is rare. These lesions are often misdiagnosed as sarcomas [3], An accurate diagnosis can only be made following surgical excision, and hyperdiploidy is associated with a more aggressive clinical picture and a higher rate of progression to sarcoma if there is recurrence [4,6,7].…”
An inflammatory myofibroblastic tumor (IMFT) is a rare entity that can arise in a multiplicity of organs including the lung, liver, and at any location within the gastrointestinal tract. Typically, an IMFT presents as a localized mass with clinical symptoms dependent upon its site of origin. IMFTs pathologically resemble a neoplastic process but are theorized to arise from an unknown inflammatory event. We present a case of a midesophageal IMFT in a 12-year-old female.
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