Title of article :
Inflammatory Myofibroblastic Tumor Report of a Rare Case in Kidney
Author/Authors :
Taheri, Diana isfahan university of medical sciences - Isfahan Kidney Diseases Research Center - Department of Pathology, ايران , Soleimani, Neda isfahan university of medical sciences - Department of Pathology, ايران , Fesharakizadeh, Mehdi islamic azad university - School of Medicine - Department of Surgery, ايران , Dolatkhah, Shahaboddin isfahan university of medical sciences - Faculty of Medicine, ايران , Kabiri, Mahmood isfahan university of medical sciences - Department of Urology, ايران , Gholipour, Abolfazl shahrekord university of medical sciences - Cellular and Molecular Research Center - Department of Medical Bacteriology, ايران
From page :
333
To page :
335
Abstract :
Inflammatory myofibroblastic tumor (IMT) is a rare neoplasm mostly seen in the lungs, but also in extrapulmonary sites. The most common genitourinary site of IMT is the bladder, but it may rarely be seen in the kidneys. We report a case of a 15-year-old girl presented with flank pain and hematuria, in which computed tomography scan revealed a mass in the left kidney. The patient underwent left nephrectomy for a diagnosis of Wilms tumor. Further assessment of the tissue demonstrated a pathologic diagnosis of IMT. Despite improvements in imaging technology, the preoperative diagnosis of IMT remains difficult and surgery is the only way for the diagnosis and treatment. Considering the role of the pathologic examination in making the definite diagnosis of IMT, we should be aware of this entity and it must be considered in the differential diagnoses.
Keywords :
plasma cell granuloma , kidney neoplasms , pediatric urology
Journal title :
Iranian Journal of Kidney Diseases (IJKD)
Journal title :
Iranian Journal of Kidney Diseases (IJKD)
Record number :
2670108
Link To Document :
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