Congenital granular cell tumor in a 2-day-old infant-An unusual situation of a dental emergency.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 36352926.
- Also identified by DOI 10.4103/jfmpc.jfmpc_2436_21 and PMC identifier 9638596.
- Licence recorded as CC BY-NC-SA.
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Abstract
Congenital granular cell tumor (CGCT) in newborns is a rare tumor occurring in the oral cavity, leading to difficulty in breast-feeding, mouth closure, and even respiration. This is rarely diagnosed perinatally and may be confused with a wide range of congenital, benign, or malignant growths during the clinical examination. The CGCT may be studied by ultrasonography to get a positive affirmation on the clinical diagnosis and, for basic pre-surgical guidance before excision. A histological study is needed to provide a final diagnosis and rule out any possible aggressive tumors. The report highlights the role of dental surgeons and clinical pathologists in providing prompt primary care for an unusual pediatric swelling under rural Indian settings.