ArticleJournal of clinical and diagnostic research : JCDR2017
Solitary Myofibroma of the Mandible in a Six-Year Old-Child: Diagnosis of a Rare Lesion.
Article in Journal of clinical and diagnostic research : JCDR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 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.
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.
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Who cites it
7 citing papers in PubMed, 15 citations in OpenAlex.
- Intraosseous myofibroma mimicking an odontogenic lesion: case report, literature review, and differential diagnosis.World journal of surgical oncology · 2024Review
- Solitary Intraosseous Myofibroma of the Mandible in a Nine-Year-Old Child: A Case Report and Literature Review.Cureus · 2024Article
- A rare case of cervical myofibroma in an infant: A case report.International journal of surgery case reports · 2024Article
- Non-familial paediatric oral myofibroma - A masquerade. Case report with a brief literature review.Journal of oral and maxillofacial pathology : JOMFP · 2023Article
- Solitary Intra-Osseous Myofibroma of the Jaw: A Case Report and Review of Literature.Children (Basel, Switzerland) · 2017Article
- Solitary Extraosseous Neurofibroma in a 5-Year-Old Child - A Case Report.Annals of maxillofacial surgeryArticle
- Mandibular Myofibroma With Impacted Teeth in a Child.The Journal of craniofacial surgeryArticle
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myofibroma is a benign uncommon fibroblastic tumour originating from the soft tissue, bone and may affect both children and adults. Radiographically myofibroma presents as unilocular radiolucency. Histologically, typical biphasic cellular arrangement is noted. Immunohistochemical markers are useful for definitive diagnosis of this uncommon neoplasm. Here, a case of six-year-old male child with a localized swelling in the left body of mandible is presented. The clinical, radiological, histological and immunohistochemical findings were corroborative of Infantile Myofibroma.
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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.