Abstract

Plexiform neurofibromas are congenital lesions associated with neurofibromatosis type 1 (NF1). They grow at variable rates, particularly in childhood, and can result in substantial morbidity and early mortality.1,2 Tumours can be multiple and extensive, and cause differing symptoms depending on their location, including pain and disfigurement, functional impairment of vision, mobility, bladder and bowel function, and respiratory compromise.

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