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Rare Hybrid Perineurioma and Granular Cell Tumor: A Pediatric Case.

作者信息

Sun Kennedy H, Goyal Sonia P, Kim Evelyn M, Mantilla-Rivas Esperanza, Rogers Gary F, Gulino Sam P

机构信息

Division of Plastic and Reconstructive Surgery, Children's National Hospital, Washington, DC, USA.

Division of Pathology and Laboratory Medicine, Children's National Hospital, Washington, DC, USA.

出版信息

Pediatr Dev Pathol. 2025 Jan-Feb;28(1):55-57. doi: 10.1177/10935266241274529. Epub 2024 Sep 9.

Abstract

We present a case of a 13-year-old patient with a distinct tumor with both granular cell and perineurial elements, located on the lower lip. The patient presented with a long-standing lip mass that was clinically felt to most likely represent a mucocele. Following surgical excision, histopathological examination revealed a well-circumscribed tumor composed of granular cells with positive S100 protein staining and spindled cells positive for EMA and GLUT-1, confirming mixed neuroectodermal and perineurial origin. This is the first case documenting a perineurial-granular cell hybrid tumor in a patient under 18 years old, and the first to be reported in the head and neck. This case expands our understanding of hybrid PNSTs, emphasizing the importance of considering diverse clinical presentations, especially in the context of rare pediatric occurrences in atypical locations.

摘要

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