| Literature DB >> 29094786 |
Luciana León Cejas1, Daniela Binaghi2, Mariano Socolovsky3, Alberto Dubrovsky4, Laura Pirra4, Cintia Marchesoni1, Ana Pardal1, Soledad Monges5, Gabriela Peretti5, Ana L Taratuto6, Fabiana Lubinieki6, Ricardo Reisin1.
Abstract
Intraneural perineurioma (IP) is an under-recognized hypertrophic peripheral nerve tumor. It affects young patients involving frequently the sciatic nerve and its branches and presents with a progressive, painless and predominantly motor deficit. Magnetic resonance neurography (MRN) is a useful tool to localize the lesion, evaluate its extension, and discriminate between different etiologies. We reviewed the clinical records of 11 patients with pathologically confirm IP. Eight patients were males with mean age 19 years. Initial complains were unilateral steppage (seven patients), bilateral steppage (one patient), unilateral gastrocnemius wasting (one patient), unilateral thigh atrophy (one patient), and unilateral hand weakness (one patient). Nine patients had mild painless sensory loss. Examinations revealed involvement of sciatic nerve extending into the peroneal nerve (eight patients), posterior tibial nerve (one patient), radial nerve (one patient), and femoral nerve (one patient). MRN revealed enlargement of the affected nerve isointense on T1-weighted, hyperintense on T2 fat-saturated images, and with avid enhancement on post-contrast imaging. In all patients, a nerve biopsy confirmed the diagnosis. MRN allows early and non-invasive identification of this tumor and is a key tool providing localization and differential diagnosis in patients with slowly progressive focal neuropathies.Entities:
Keywords: intraneural perineurioma; magnetic resonance neurography; peripheral nerve tumors; peroneal nerve; sciatic nerve; tibial nerve
Mesh:
Year: 2017 PMID: 29094786 DOI: 10.1111/jns.12240
Source DB: PubMed Journal: J Peripher Nerv Syst ISSN: 1085-9489 Impact factor: 3.494