Plexiform fibrohistiocytic tumor in the submandibular region: A rare diagnosis
Pahwa R., Khurana N.
Laboratory Study, published in Indian J Otolaryngol Head Neck Surg (2010) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Laboratory Study
- Journal
- Indian J Otolaryngol Head Neck Surg (2010)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 23120712
- PMCID
- PMC3450309
- DOI
- 10.1007/s12070-010-0028-2
Abstract (original English)
Plexiform fibrohistiocytic tumor (PFHT) is a rare mesenchymal neoplasm of intermediate malignancy, first reported by Enzinger and Zhang in 1988 [1]. It mainly affects children and young adults and preferentially involves the upper extremity [1, 2].We report a rare case in the submandibular region which was diagnosed on histopathology.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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