A diagnostically challenging case of inflammatory myofibroblastic tumor primary to the peritoneum

Author:

Karibe Jurii1ORCID,Teranishi Jun‐ichi1,Kawahara Takashi1ORCID,Noguchi Takeaki1ORCID,Takeshima Teppei1ORCID,Osaka Kimito1,Kumagai Eita2,Sawazumi Tomoe2,Fujii Satoshi234,Uemura Hiroji1

Affiliation:

1. Department of Urology and Renal Transplantation Yokohama City University Medical Center Yokohama Japan

2. Department of Pathology Yokohama City University Medical Center Yokohama Japan

3. Department of Pathology Yokohama City University Hospital Yokohama Japan

4. Department of Molecular Pathology Yokohama City University Graduate School of Medicine Yokohama Japan

Abstract

IntroductionInflammatory 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 presentationThe 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.ConclusionWe 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.

Publisher

Wiley

Reference17 articles.

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4. A case of ALK‐negative inflammatory myofibroblastic tumor originating from the greater omentum in a sixteen‐year‐old;Maehara T;Jpn. J. Diagn. Pathol.,2021

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