Göksügür, NadirGürel, Safiye2021-06-232021-06-2320111075-122Xhttps://doi.org/10.1111/j.1524-4741.2011.01102.xhttps://hdl.handle.net/20.500.12491/6925Neurofibromatosis type I or von Recklinghausendisease is an autosomal-dominant condition withwell-known clinical signs, including cafe ́au laitpatches, axillary freckling, Lisch nodules, and multipleneurofibromas. A 41-year-old woman presented to ourunit with severe neurofibromatosis of nipple-areolacomplex (NAC) like a bunch of grapes, associatedwith multiple neurofibromas of the trunk and limbs(Fig. 1a). Bilateral bunch of neurofibromas arisingfrom the NAC associated with numerous cutaneousneurofibromas are illustrated in a reconstructed axialMRI image with VRD (volume rendering display)technique (Fig. 1b)eninfo:eu-repo/semantics/closedAccessNipple-AreolaEditorial10.1111/j.1524-4741.2011.01102.x174424424216158222-s2.0-79960429910Q2WOS:000292743100018Q3