Fibrous hamartoma of infancy with sarcomatous transformation: an unusual morphology

Authors

DOI:

https://doi.org/10.4322/acr.2021.380

Keywords:

Hamartoma, Neoplasms, Fibrous Tissue, Neoplasms, Connective Tissue, Neoplasms, Connective and Soft Tissue

Abstract

Background: Fibrous hamartoma of infancy (FHI) is a rare soft tissue lesion arising as a subcutaneous mass involving the axilla, trunk, and upper arm in infants and children <2yrs. Sarcomatous transformation in FHI is described in anecdotal cases in the literature. Case Report: We describe one such example arising as a mass in the lower back in a 3-month-old infant. On histology, the tumor contained classic triphasic morphology; however, brisk mitotic activity noted at multiple foci was diagnostically challenging to categorize. The tumor was evaluated for ETV6-NTRK3 fusion to exclude other common differentials. Conclusion: While FHI may be frequently encountered in infants, rare sarcomatous transformation are known to occur and merits special attention as it can be misdiagnosed. Also, a close follow-up is warranted as the lesion is known to recur locally.

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References

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Published

2022-06-23

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Section

Clinical Case Report

How to Cite

Gargi Kapatia, Debajyoti Chatterjee, Kirti Gupta, & Amita Trehan. (2022). Fibrous hamartoma of infancy with sarcomatous transformation: an unusual morphology. Autopsy and Case Reports, 12, e2021380. https://doi.org/10.4322/acr.2021.380