Postauricular congenital alveolar rhabdomyosarcoma- a case report of an unusual entity
2006
Case Report of Congenital Alveolar Rhabdomyosarcoma
Sample size: 1
publication
Evidence: low
Author Information
Author(s): Vankalakunti Mahesha, Das Ashim, Rao Narasimhan KL
Primary Institution: Postgraduate Institute of Medical Education & Research, Chandigarh, India
Conclusion
Congenital alveolar rhabdomyosarcoma is a rare and highly malignant tumor, and this case highlights its unusual presentation in the post-auricular region.
Supporting Evidence
- Congenital alveolar rhabdomyosarcoma is extremely uncommon and usually fatal.
- The tumor was completely resected with no recurrence or metastasis after one year.
- Histological examination confirmed the diagnosis of congenital alveolar rhabdomyosarcoma.
Takeaway
This study talks about a rare type of cancer found in a baby that was removed through surgery, and the baby did not have any problems after a year.
Methodology
The mass was surgically resected and diagnosed through histological examination.
Limitations
Only one case is reported, limiting the generalizability of the findings.
Participant Demographics
An 18-month-old male child.
Digital Object Identifier (DOI)
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