| Literature DB >> 29469988 |
Tim Godel1, Victor-Felix Mautner2, Said Farschtschi2, Mirko Pham1,3, Daniel Schwarz1, Moritz Kronlage1, Isabel Gugel4, Sabine Heiland1, Martin Bendszus1, Philipp Bäumer1,5.
Abstract
Schwannomatosis and neurofibromatosis type 2 are hereditary tumor syndromes, and peripheral neuropathy has been reported in both. We prospectively applied in vivo morphometric measurement of dorsal root ganglia volume in 16 schwannomatosis patients, 14 neurofibromatosis type 2 patients, and 26 healthy controls by magnetic resonance neurography. Compared to healthy controls, dorsal root ganglia hypertrophy was a consistent finding in neurofibromatosis type 2 (L3, + 267%; L4, + 235%; L5, + 241%; S1, + 300%; S2, + 242%; Bonferroni-adjusted p < 0.001) but not in schwannomatosis. Dorsal root ganglia may be a vulnerable site in origination of areflexia and sensory loss and a useful diagnostic marker in neurofibromatosis type 2. Ann Neurol 2018;83:854-857.Entities:
Mesh:
Year: 2018 PMID: 29469988 DOI: 10.1002/ana.25191
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422