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. 2013 Mar-Apr;7(3-4):E237-40.
doi: 10.5489/cuaj.544.

Inflammatory myofibroblastic tumour of the bladder: Case report and review of the literature

Affiliations

Inflammatory myofibroblastic tumour of the bladder: Case report and review of the literature

Li Wei et al. Can Urol Assoc J. 2013 Mar-Apr.

Abstract

Inflammatory myofibroblastic tumour (IMT) is a rare tumour with malignant potential, and has been described in many major organs. However, bladder location is very uncommon. We report the case of a 23-year-old woman who presented with painless gross hematuria for 2 weeks. Contrast-enhanced computed tomography revealed a bladder tumour. The patient underwent an open partial cystectomy and the final pathologic diagnosis was IMT of bladder. Typical IMTs can be locally aggressive, therefore close follow-up is necessary.

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Figures

Fig. 1
Fig. 1
Contrast-enhanced computed tomography showed a round mass arising from the wall of the bladder dome and with deep muscle invasion, the mass could be enhanced non-uniformly.
Fig. 2
Fig. 2
Inflammatory myofibroblastic tumors cells were spindle to stellate in shape, widely separated or showed a compact fascicular pattern (hematoxylin and eosin stain, ×100).
Fig. 3
Fig. 3
Image shows the invasion of muscularis propria (hematoxylin and eosin stain, ×100).
Fig. 4
Fig. 4
Image shows typical mitotic figures (white arrow, hematoxylin and eosin stain, ×200).

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