This case reports a painful subcutaneous nodule with both granular cell tumor and nevus spilus, suggesting a potential developmental association.
Granular cell tumors (GCTs) are rare neoplasms believed to originate from Schwann cells, exhibiting immunohistochemical and ultrastructural features consistent with neural crest derivation. Similarly, a nevus spilus (NS) is a pigmented skin lesion composed of lentiginous background macules with superimposed darker macules or papules, also thought to arise from neural crest-derived melanocytes. We report a unique case of a 27-year-old female who presented with a painful subcutaneous nodule on the left medial midback, overlaid by an NS. Surgical excision revealed a lesion consistent with a GCT based on histopathologic evaluation. To our knowledge, this is one of the few reported cases demonstrating spatial co-localization of a GCT and NS. This case raises the possibility of a shared embryologic origin contributing to the concurrent development of both lesions in the same anatomic location. Further research is needed to explore whether this reflects a coincidental overlap or an underlying developmental association between neural crest-derived cutaneous proliferations.
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Moreno‐Küstner et al. (2025) studied this question.
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