| Literature DB >> 35586084 |
Anatoly Budylev1, Irit Solar2, Rivka Kessner1,3, Asaf Aizic2.
Abstract
Inflammatory Myofibroblastic Tumors (IMTs) are rare fibroblastic/myofibroblastic neoplasms that affect predominately pediatric patients and young adults. Almost half of the patients with IMTs have a chromosomal abnormality in the Anaplastic Lymphoma Kinase 1 gene on chromosome 2p23. Although these tumors occur primarily in the lung, lesions have been reported in a variety of intra-abdominal organs like the liver, spleen, and mesentery. Small bowel IMTs are particularly rare. IMTs generally pursue a benign clinical course, however intra-abdominal and retroperitoneal tumors have typically shown higher local recurrence and even distant metastases. The most common presenting symptoms of an intra-abdominal IMT are abdominal pain and change in bowel habits. Laboratory results are nonspecific and can include anemia and minor elevation of inflammatory markers like C-reactive protein. We report an unusual case of IMT in the small bowel causing the obstruction. Copyright Journal of Radiology Case Reports.Entities:
Keywords: Bowel solitary mast cell tumor; Inflammatory Myofibroblastic Tumor; Inflammatory pseudotumor; Small bowel obstruction; extra-pulmonary Inflammatory Myofibroblastic Tumors
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Year: 2022 PMID: 35586084 PMCID: PMC9063829 DOI: 10.3941/jrcr.v16i1.3928
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922