ArticleCureus2026
Uterine Inflammatory Myofibroblastic Tumor: A Case Report.
Article in Cureus, 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
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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
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Uterine inflammatory myofibroblastic tumor (IMT) is a rare type of mesenchymal tumor that usually follows an indolent course, although it can behave aggressively in a minority of cases. The most common clinical presentations are abnormal uterine bleeding and pelvic discomfort. Radiographic features are non-specific, typically showing a myometrial mass with heterogeneous enhancement and, occasionally, infiltrative margins. Histologically, IMTs are composed of spindle myofibroblasts in a myxoid to compact stroma with an inflammatory infiltrate, and they often exhibit anaplastic lymphoma kinase (ALK) gene fusions and ALK positivity. The main treatment approach is surgical excision, with ALK inhibitors as a therapeutic option in selected cases.
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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.