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A diagnostically challenging case of inflammatory myofibroblastic tumor primary to the peritoneum.
Karibe, Jurii; Teranishi, Jun-Ichi; Kawahara, Takashi; Noguchi, Takeaki; Takeshima, Teppei; Osaka, Kimito; Kumagai, Eita; Sawazumi, Tomoe; Fujii, Satoshi; Uemura, Hiroji.
Afiliación
  • Karibe J; Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan.
  • Teranishi JI; Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan.
  • Kawahara T; Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan.
  • Noguchi T; Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan.
  • Takeshima T; Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan.
  • Osaka K; Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan.
  • Kumagai E; Department of Pathology Yokohama City University Medical Center Yokohama Japan.
  • Sawazumi T; Department of Pathology Yokohama City University Medical Center Yokohama Japan.
  • Fujii S; Department of Pathology Yokohama City University Medical Center Yokohama Japan.
  • Uemura H; Department of Pathology Yokohama City University Hospital Yokohama Japan.
IJU Case Rep ; 7(3): 206-209, 2024 May.
Article en En | MEDLINE | ID: mdl-38686080
ABSTRACT

Introduction:

Inflammatory myofibroblastic tumors are difficult to diagnose because of the lack of specific indicators. We describe a diagnostically challenging case of an inflammatory myofibroblastic tumor primary to the peritoneum. Case presentation The patient was a 25-year-old male who presented at our hospital with lower abdominal pain. Computed tomography revealed a mass lesion 80 mm in diameter just above the bladder. This was suspected to be a bleeding tumor of the urachus. Since malignancy could not be ruled out, surgery was planned. This revealed a fragile tumor arising from the peritoneum. Following its removal, the tumor was diagnosed by histopathological analysis as an inflammatory myofibroblastic tumor.

Conclusion:

We describe a case of inflammatory myofibroblastic tumor primary to the peritoneum diagnosed by histopathology. Inflammatory myofibroblastic tumor should be considered in the differential diagnosis of abdominal wall and anterior bladder tumors.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: IJU Case Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: IJU Case Rep Año: 2024 Tipo del documento: Article