Literature DB >> 32522650

Limb Undergrowth in Intraneural Perineuriomas: An Under-Recognized Association.

Courtney Pendleton1, Karina A Lenartowicz1, B Matthew Howe1, Robert J Spinner2.   

Abstract

BACKGROUND: Intraneural (IN) perineuriomas are a rare benign hypertrophic nerve tumor, most frequently occurring in young patients. Patients with IN perineurioma have been anecdotally found to have limb undergrowth; however, this has not been systematically evaluated.
METHODS: Archived electronic records from 1990 to 2018 from a single institution were reviewed for pathology or radiology reports documenting a diagnosis of IN perineurioma. This identified 111 patients; 3 patients with IN perineurioma of cranial nerves were excluded. We further reviewed the 108 patients and identified those with a documented limb length discrepancy (LLD) or hand/foot size discrepancy (HFD) and tried to correlate findings with nerve-territory distribution.
RESULTS: Twenty-seven (25.0%) patients had either LLD or HFD. Nine patients had only an LLD, 6 patients had only an HFD, and 12 patients had both. Patients with undergrowth were significantly younger at diagnosis than patients without (6.14 vs. 22.9 years, respectively). Although there was a trend toward a greater incidence of LLD in lower extremity IN perineuriomas, this was not statistically significant. Patients with proximal IN perineuriomas had a higher incidence of LLD or HFD than patients with distal IN perineuriomas. The difference between the 2 groups was statistically significant (P < 0.0001). All instances of undergrowth were explained by nerve-territory bone innervation.
CONCLUSIONS: Limb undergrowth occurs in the affected nerve territory and is likely under-reported in patients with IN perineuriomas. Within our series, patients with documented LLD and HFD were likely to be significantly younger at diagnosis than patients without undergrowth.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Intraneural perineurioma; Joint dysplasia; Limb length discrepancy; Neuromuscular choristoma; Perineurioma

Mesh:

Year:  2020        PMID: 32522650     DOI: 10.1016/j.wneu.2020.05.280

Source DB:  PubMed          Journal:  World Neurosurg        ISSN: 1878-8750            Impact factor:   2.104


  1 in total

1.  Frequent CTNNB1 p.S45 Mutations and Aggressive Clinical Behavior in Neuromuscular Choristoma-Associated Fibromatosis.

Authors:  Jodi M Carter; Andres A Maldonado; B Matthew Howe; Scott Okuno; Robert J Spinner
Journal:  Neurosurgery       Date:  2021-03-15       Impact factor: 4.654

  1 in total

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