Abstract
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.
MeSH terms
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Asthma / pathology
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Child
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Cyclooxygenase 2 Inhibitors / therapeutic use
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Deglutition Disorders / etiology
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Diagnosis, Differential
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Digestive System Surgical Procedures
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Endoscopy, Digestive System
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Epstein-Barr Virus Infections / pathology
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Esophageal Diseases / pathology*
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Esophageal Diseases / physiopathology
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Esophageal Diseases / therapy
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Female
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Gastroesophageal Reflux / pathology
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Granuloma, Plasma Cell / pathology*
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Granuloma, Plasma Cell / physiopathology*
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Granuloma, Plasma Cell / therapy
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Herpes Zoster / pathology
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Humans
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Hypernatremia / etiology
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Immunohistochemistry
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Magnetic Resonance Imaging
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Polyps / pathology
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Tomography, X-Ray Computed
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Vomiting / etiology
Substances
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Cyclooxygenase 2 Inhibitors