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Recurrent Giant Cell Fibroblastoma in an Infant: A Diagnostic Challenge
Priyanka Maity1, Uttara Chatterjee1, Mou Das1
1Department of Pathology, Institute of Postgraduate Medical Education and Research, Kolkata, India.
Insights
Giant cell fibroblastoma (GCF) can mimic sarcoma. This case highlights GCF recurrence despite chemotherapy, with characteristic giant cells aiding diagnosis over embryonal rhabdomyosarcoma.
Area of Science:
- Pathology
- Pediatric Oncology
- Dermatopathology
Background:
- Giant cell fibroblastoma (GCF) presents diverse morphological features.
- These features can lead to misdiagnosis, particularly as sarcoma.
- Distinguishing GCF from other pediatric tumors is crucial for appropriate management.
Abstract:
Background: Giant cell fibroblastoma (GCF) shows a wide spectrum of morphological patterns which may lead to a misdiagnosis of sarcoma. Case Report: This 14- month- old baby was referred to us for recurrent left scrotal embryonal rhabdomyosarcoma (ERMS), first diagnosed at 8 months, status post chemotherapy. Review of previous histology, cytology (with frequent multinucleated floret type giant cells but without cross striations) and immunohistochemistry resulted in the change of diagnosis to GCF. It was re-excised, recurred at 20 months of age, and was again re-excised. The morphology was the same in both recurrences as the original. Conclusion: Despite chemotherapy, the histology of multiple recurrences for GCF remained the same as the original. Cytologically, identification of the multinucleated floret like giant cells without cross striations was helpful in differentiating this lesion from embryonal rhabdomyosarcoma.
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