Mesenteric inflammatory myofibroblastic tumors in an elder patient with early recurrence: A case report

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Mesenteric inflammatory myofibroblastic tumors

Inflammatory myofibroblastic tumors (IMTs), also known as inflammatory pseudotumors and inflammatory fibrosarcomas, are uncommon mesenchymal tumors composed of myofibroblastic spindle cells admixed with lymphocytes, plasma cells and eosinophils. Once thought to be reactive, these lesions are now considered to be neoplastic. These tumors can occur throughout the body, most commonly in the lung, ...

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Maxillary Sinus Inflammatory Myofibroblastic Tumors: A Review and Case Report

An inflammatory myofibroblastic tumor (IMT) is an immunohistochemically diverse entity demonstrating neoplastic and nonneoplastic qualities. Although IMTs can arise in any area of the body, lesions arising in certain sites, namely, the nasal cavity, paranasal sinuses, and pterygopalatine fossa, demonstrate a heightened neoplastic and invasive potential. Despite case specific complete tumor regr...

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Inflammatory Myofibroblastic Tumor of the Larynx: A Case Report

Introduction: Inflammatory myofibroblastic pseudotumors are initially described in the lung and various extrapulmonary sites such as the orbits, palatine tonsils, ears, gingiva, pterygomaxillary space, and periodontal tissues. These tumors rarely involve the larynx and predilection to the glottis occurs in an indolent manner.   Case Report This case describes a laryngeal myofibroblastic tumor i...

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Inflammatory Myofibroblastic Tumors in a Case with Hypogastric Discomfort

BACKGROUND Inflammatory myofibroblastic tumors (IMTs) are scarce tumors with discrete immunohistochemical and molecular attributes which are not related to a particular location. There are different reports about the intrinsic nature of these tumors as benign to possibly malignant. CASE REPORT Here we report the case of a 68-year-old man referred to the Internal Medicine Department of Razi Hosp...

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ژورنال

عنوان ژورنال: World Journal of Gastroenterology

سال: 2007

ISSN: 1007-9327

DOI: 10.3748/wjg.v13.i26.3645