Abstract

Introduction: Inflammatory myofibroblastic tumors (IMTs) are uncommon mesenchymal lesions classified by WHO as neoplasms of uncertain behavior. Morphologically, IMTs are composed of proliferating spindled myofibroblastic cells accompanied by a marked - usually chronic - inflammatory infiltrate. The etiology is unknown, but several theories have been suggested, including an association with Wilms’ tumor. IMTs are rarely diagnosed in adults and have been reported in various organs. IMTs are considered benign but with a potential to recur at their primary site. Case report: A 44-year-old female experienced intermittent severe abdominal pain, loose stools and a visible abdominal bulge. In early childhood the patient had been treated for a Wilms’ tumor. At admission Meckel’s diverticulitis was suspected, but during surgery a tumor in the terminal ileum, creating a conglomerate of small intestinal loops, was observed and completely resected. The pathology report characterized the tumor as a histologically benign inflammatory myofibroblastic tumor. Postoperatively, the patient experienced several complications including an anastomotic leakage and subsequent formation of an abscess and transcutaneous fistula. Discussion: IMTs rarely arise in the small intestine, and to our knowledge the manifestation of a small intestine conglomerate has not been described previously. Making the diagnosis is difficult, and numerous differential diagnoses were possible in this case. Approximately 8-25% of IMTs in the gastrointestinal tract recur locally. Complete surgical resection is the treatment of choice, and re-excision is the preferred therapy for local recurrence. To our knowledge, no guidelines concerning follow-ups are available. Conclusion: IMTs in the terminal ileum can mimic Meckel’s diverticulitis and present with symptoms of obstructive ileus due to the formation of a conglomerate of small intestinal loops. Furthermore, IMTs should be considered as a diagnostic possibility in patients with a past medical history of Wilms’ tumor.

Highlights

  • Inflammatory myofibroblastic tumors (IMTs) are uncommon mesenchymal lesions classified by WHO as neoplasms of uncertain behavior

  • IMTs should be considered as a diagnostic possibility in patients with a past medical history of Wilms’ tumor

  • This report presents a case of an IMT in the terminal ileum in a female adult, treated for Wilms’ tumor in childhood

Read more

Summary

15 May 2017

Any reports and responses or comments on the article can be found at the end of the article. IMTs should be considered as a diagnostic possibility in patients with a past medical history of Wilms’ tumor. Keywords Wilms’ tumor, inflammatory myofibroblastic tumors, IMTs, neoplasms of uncertain behavior, ileal conglomerate, ileus. The author information of Rikke Raagaard Soerensen is changed to Department of Pathology, Herlev Hospital, University of Copenhagen, Herlev, Copenhagen, Denmark instead of Department of Pathology, Hvidovre Hospital, University of Copenhagen, Hvidovre, Copenhagen, Denmark. Rikke Raagaard Soerensen was during this work employed at Herlev Hospital

Introduction
Discussion
Findings
Conclusion
Chaudhary P
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.