Ectomesenchymal chondromyxoid tumor: Review of literature and a report of a rare case
2011

Ectomesenchymal Chondromyxoid Tumor: A Rare Case in a Child

Sample size: 1 publication Evidence: low

Author Information

Author(s): Leeky Mohanty, Narayan TV Shenoy, Sadhana Jamadar, Saleha

Primary Institution: The Oxford Dental College, Hospital and Research Centre

Hypothesis

What are the clinical and histopathological features of ectomesenchymal chondromyxoid tumor (ECMT) in a pediatric patient?

Conclusion

This case highlights the rarity of ectomesenchymal chondromyxoid tumor in children and emphasizes the need for awareness of this distinct entity.

Supporting Evidence

  • Ectomesenchymal chondromyxoid tumor is a rare benign tumor with only 40 cases reported in literature.
  • The tumor typically presents as a slow-growing, painless swelling on the anterior dorsum of the tongue.
  • Histopathological examination showed a lobular growth pattern with infiltrative characteristics.

Takeaway

Ectomesenchymal chondromyxoid tumor is a rare, benign tumor that can occur in children, and it usually appears as a painless swelling on the tongue.

Methodology

The case was diagnosed through clinical examination, ultrasound, FNAC, and histopathological examination.

Limitations

The study is based on a single case report, limiting the generalizability of the findings.

Participant Demographics

A 7-year-old boy.

Digital Object Identifier (DOI)

10.4103/0973-029X.80021

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