ReviewMedical molecular morphology2014
Solitary myofibroma of the mandible: an immunohistochemical and ultrastructural study with a review of the literature.
Review in Medical molecular morphology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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.
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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.
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Who cites it
6 citing papers in PubMed, 25 citations in OpenAlex.
- Myofibromas of the jawbones in pediatric patients. A clinicopathological study.Medicina oral, patologia oral y cirugia bucal · 2025Article
- Head and neck myofibroma: A case series of 16 cases and literature review.Medicina oral, patologia oral y cirugia bucal · 2024Review
- Article
- Oral myofibroma presenting as an aggressive gingival lesion.BMJ case reports · 2021Article
- Aggressive Intraosseous Myofibroma of the Maxilla: Report of a Rare Case and Literature Review.Head and neck pathology · 2021Review
- Solitary intraosseous myofibroma of the tibia in an adult patient: A case report.Journal of bone oncology · 2014Article
Corrections and comments
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Authors and funding
9 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A solitary myofibroma (MF) is an unusual spindle cell neoplasm that usually arises in the soft tissue, skin, or bone of the head and neck region in infancy. We report an extremely rare case of MF of the mandible in an 18-year-old Japanese woman together with the conventional histologic, immunohistochemical, and electron microscopic findings. The tumor was well circumscribed and composed of fibroblast-like or myofibroblast-like spindle cells. On immunohistochemical evaluation the tumor cells were positive for vimentin, α-smooth muscle actin, HHF-35, and calponin, but negative for neurogenic antigens and markers for vascular endothelial cells. The Ki-67 labeling index was 10 % and the p53 labeling index was 10 %. Ultrastructural examination revealed smooth muscle cell differentiation. The patient was treated by surgical resection and underwent follow-up without any signs of recurrence. MF presents a wide range of differential diagnosis, including benign and malignant neoplasms. Therefore, accurate diagnosis may avoid an unnecessarily aggressive therapy.
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Registered trials
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