ArticleRadiology case reports2026
Inflammatory myofibroblastic tumor of omentum mimicking an ovarian lesion: A case report.
Article in Radiology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Inflammatory myofibroblastic tumor (IMFT) is a neoplastic entity with intermediate malignant potential, characterized by its tendency for local recurrence and, rarely, distant metastasis. It most often occurs in the lung, while extra-pulmonary sites, like the omentum, are rare and present with non-specific clinical and radiologic features, making diagnosis challenging. A 6-year-old girl presented with a 2-month history of intermittent fever, a painless abdominal lump, elevated inflammatory markers, and an ultrasound impression suggestive of an ovarian neoplasm, while magnetic resonance imaging (MRI) showed a right iliac fossa mass separate from the ovary with persistent enhancement. Laparoscopic resection identified the lesion arising from the greater omentum, and histopathology with immunohistochemistry confirmed the diagnosis of IMFT. Omental IMFT is rare and often mimics ovarian or other intra-abdominal tumors, making multimodality imaging, particularly magnetic resonance imaging, crucial for lesion localization and narrowing the differential diagnosis. Although histopathology confirms the diagnosis and complete surgical resection typically yields excellent outcomes, long-term follow-up remains essential due to the risk of recurrence.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.