Inflammatory myofibroblastic tumor: a rare clinical case of bladder pathology
https://doi.org/10.21886/2308-6424-2025-13-6-132-141
Abstract
Inflammatory myofibroblastic tumor (IMT) is a rare neoplasm characterized by proliferation of spindle‑shaped cells with prominent inflammatory cell infiltration. IMT is also referred to as an inflammatory pseudotumor or pseudosarcomatous myofibroblastic tumor. Although it accounts for less than 1% of all bladder tumors, the bladder is the most frequent site of IMT within the genitourinary tract. In this report, we present the case of patient M., a 1‑year‑7‑month‑old child with a 2‑month history of dysuria and painful voiding. Following a diagnostic work‑up, including ultrasound, voiding cystography, abdominal and pelvic CT, cystourethroscopy, and pelvic MRI, the child underwent surgical excision (enucleation) of the mass with negative margins. Histopathological examination confirmed the diagnosis of IMT. During 2 years of follow‑up with ultrasound, CT, and MRI, no evidence of local recurrence was detected, which is consistent with published data indicating low recurrence rates after organ‑sparing surgical management without adjuvant chemotherapy.
About the Authors
D. A. DobroserdovРоссия
Dmitrii A. Dobroserdov – Cand.Sc.(Med)
Saint Petersburg
M. P. Kuchinsky
Россия
Mikhail P. Kuchinskii
Saint Petersburg
N. A. Filatova
Россия
Natalia A. Filatova
Saint Petersburg
M. M. Kardanov
Россия
Marat M. Kardanov
Saint Petersburg
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Review
For citations:
Dobroserdov D.A., Kuchinsky M.P., Filatova N.A., Kardanov M.M. Inflammatory myofibroblastic tumor: a rare clinical case of bladder pathology. Urology Herald. 2025;13(6):132-141. (In Russ.) https://doi.org/10.21886/2308-6424-2025-13-6-132-141
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