Rt. Kloos et al., BONE SCANS IN NEUROFIBROMATOSIS - NEUROFIBROMA, PLEXIFORM NEUROMA ANDNEUROFIBROSARCOMA, The Journal of nuclear medicine, 37(11), 1996, pp. 1778-1783
Neurofibromatosis type 1 or von Recklinghausen's disease is one of the
most common autosomal dominant genetic disorders. Between 29% and 77%
of patients may suffer from a wide range of skeletal abnormalities an
d, thus, patients with neurofibromatosis frequently undergo skeletal s
cintigraphy, at which lime the common peripheral nerve soft-tissue tum
ors that occur in this syndrome (neurofibromas, plexiform neuromas and
neurofibrosarcomas) may be demonstrated. Methods: Single or multiphas
e Tc-99m methylenediphosphonate (MDP) bone scans were performed in fiv
e patients with neurofibromatosis as part of their clinical evaluation
. Results: We imaged neurofibrosarcomas in three patients, cutaneous n
eurofibromas in one patient and a plexiform neuroma in one patient. Co
nclusion: Single- or multiphasic bone scans may localize common soft-t
issue tumors in neurofibromatosis.