Inflammatory myofibroblastic tumor of the urinary bladder: differential diagnosis.

Inflammatory myofibroblastic tumor (IMT) is a rare proliferative lesion that needs to be differentiated particularly from sarcoma and sarcomatoid carcinoma. We describe a 57-year-old male with IMT of the bladder who presented with the complaints of pelvic pain, hematuria, malaise, weight loss and dy...

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Published in:Turkiye Klinikleri Journal of Medical Sciences Vol. 30; no. 6; pp. 2067 - 2072
Main Authors: Eliyatkin, Nuket, Günlüsoy, Bülent, Olgun, Alev Gülsah, Sezgin, Arsenal, Postaci, Hakan
Format: case study pictorial Journal Article
Published: Turkiye Klinikleri Dec2010
Online Access:View this record in EBSCOhost
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      dt: Dec2010
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      pub: Turkiye Klinikleri
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        atl: Inflammatory myofibroblastic tumor of the urinary bladder: differential diagnosis.
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        au:
          Eliyatkin, Nuket
          Günlüsoy, Bülent
          Olgun, Alev Gülsah
          Sezgin, Arsenal
          Postaci, Hakan
        affil: Departments of Pathology, Urology, Izmir Bozyaka Education and Research Hospital, Izmir
      sug:
        subj:
          Bladder Neoplasms Diagnosis
          Male
          Middle Age
          Middle Aged: 45-64 years
          Male
      ab: Inflammatory myofibroblastic tumor (IMT) is a rare proliferative lesion that needs to be differentiated particularly from sarcoma and sarcomatoid carcinoma. We describe a 57-year-old male with IMT of the bladder who presented with the complaints of pelvic pain, hematuria, malaise, weight loss and dysuria. Ultrasonography revealed a mass 4 cm in diameter in the bladder. On computed tomography, a hyperdense, nodular mass with the maximum size of 4 cm was detected on the right lateral wall of the bladder. The bladder mass was excised by transurethral resection. Pathologic findings revealed that the tumor had spindle-shaped cells with eosinophilic cytoplasm in myxoid stroma with abundant inflammatory infiltrate. There has been no evidence of recurrent tumor in 45 months postoperatively. It is concluded that IMT needs to be differentiated particularly from sarcoma and sarcomatoid carcinoma.
      pubtype: Academic Journal
      doctype:
        case study
        pictorial
        Journal Article
      ougenre: Article
    language: English
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