We report the case of a 4-year-old child with a rare solitary neurofibroma-schwannoma hybrid tumor in the brachial plexus, not associated with known syndromes. Surgical management through a transclavicular approach enabled complete tumor excision with favorable postoperative outcomes. Histopathology and immunohistochemistry confirmed the tumor's hybrid nature.
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|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11521212 | PMC |
| http://dx.doi.org/10.4103/jiaps.jiaps_75_24 | DOI Listing |
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