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Cervical congenital infantile fibrosarcoma: a case report
Alisha Gupta1, Shilpa Sharma2, Sandeep Mathur3
1Department of Pediatric Surgery, All India Institute of Medical Sciences, New Delhi, India.
Insights
Congenital infantile fibrosarcoma, a rare neck tumor in infants, was successfully managed with surgical excision. This case highlights the importance of considering this rare diagnosis in congenital neck masses, often misdiagnosed as lympho-venous malformations.
Area of Science:
- Pediatric Oncology
- Surgical Pathology
- Rare Pediatric Tumors
Background:
- Congenital infantile fibrosarcoma is a rare mesenchymal tumor affecting infants and adults.
- The congenital variant is exceptionally rare, with limited documented cases, particularly in the neck.
- This report details a successfully managed case of congenital infantile fibrosarcoma in the neck.
Observation:
- A 3-month-old infant presented with a congenital neck swelling.
- Initial clinical diagnosis suggested lympho-venous malformation.
- Excisional biopsy was performed due to a low suspicion of malignancy.
Findings:
- Histopathology confirmed the diagnosis of congenital infantile fibrosarcoma.
- This represents a rare instance of successful surgical management for this specific tumor location.
- The tumor was initially misdiagnosed, underscoring diagnostic challenges.
Implications:
- Congenital infantile fibrosarcoma should be considered in the differential diagnosis of congenital neck masses.
- Accurate histopathological examination is crucial for definitive diagnosis.
- Successful surgical excision offers a viable management strategy for this rare condition.
Background:
Congenital infantile fibrosarcoma is a rare mesenchymal tumor seen in children as well as adults. The congenital variety is rare and out of the reported cases only one case sited in the neck has been reported so far. Another such case is presented here who was successfully managed.
Case Presentation:
A 3-month-old Hindu baby boy presented with a congenital neck swelling. The apparent clinical diagnosis was lympho-venous malformation. With a remote possibility of malignancy, an excisional biopsy was done. Histopathology revealed congenital infantile fibrosarcoma.
Conclusion:
A successful excision of cervical congenital infantile fibrosarcoma has not been reported. This diagnosis should be kept as a possibility in all congenital cervical swellings. These are commonly misdiagnosed as lympho-venous malformations and histopathology is confirmatory.
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