scholarly journals Intraneural perineurioma

2020 ◽  
Author(s):  
2015 ◽  
Vol 41 (8) ◽  
pp. 885-886
Author(s):  
N. J. Visser ◽  
H. Bril ◽  
J. van Loon

2020 ◽  
Vol 129 (1) ◽  
pp. e49-e50
Author(s):  
PAMELA OLIVEIRA SANTOS ◽  
CRISTIANE CANTIGA DA SILVA ◽  
TIAGO NOVAES PINHEIRO

2012 ◽  
Vol 7 (1) ◽  
pp. 649 ◽  
Author(s):  
Efrat Saraf Lavi ◽  
Allan D Levi ◽  
Erica K. Schallert ◽  
Andrew D. Brown ◽  
Michael D. Norenberg

Author(s):  
Douglas D Damm ◽  
Dean K White ◽  
Jerry D Merrell

2019 ◽  
Vol 90 (3) ◽  
pp. e21.3-e20
Author(s):  
Mahima Kapoor ◽  
Kirsten Pierce ◽  
Annelies Quaegebeur ◽  
Michael P Lunn ◽  
Aisling S Carr ◽  
...  

ObjectivesIntraneural perineurioma is a rare, benign neoplasm of peripheral nerve. The histopathological features are well defined.DesignWe describe 5 cases of histologically confirmed perineuriomas and 14 cases diagnosed on clinical and radiological characteristics to highlight the features of this rare entity.MethodsWe identified cases from the imaging and histopathology database and conducted a retrospective case note review.ResultsThe subjects include 7 men and 12 women, with mean (standard deviation) age of 17.64 (13) years at onset of symptoms. 14 of the 15 lower limb cases were located in the sciatic nerve or its divisions. 1 each was identified in ulnar, median and radial nerves and 1 case was in a facial nerve. The MRI features were homogenous between the groups. The nerves biopsied included 1 tibial, 1 ulnar, 1 radial, 1 facial and 1 sciatic all showing classic pathology findings. 2 patients, interestingly, had coincidental intracranial meningioma, given the recent discovery of a potential shared pathogenesis (mutations in TRAF7) with intracranial meningiomas. 2 patients had ‘skip lesions’ within the same nerve and 3 patients had foraminal and extraforaminal involvement of lumbosacral nerve roots.ConclusionsOur unit now favours the clinicoradiological features for diagnosing perineuriomas rather than performing a biopsy on all patients. Also, the potential shared pathogenesis with meningiomas raises the clinical issue of screening in patients with perineuriomas but more clinical evidence is required.


Neurology ◽  
2012 ◽  
Vol 78 (Meeting Abstracts 1) ◽  
pp. P05.146-P05.146
Author(s):  
M. Mauermann ◽  
C. Klein ◽  
P. Dyck ◽  
J. Engelstad ◽  
H. Flynn Gilmer ◽  
...  

2001 ◽  
Vol 26 (2) ◽  
pp. 168-170 ◽  
Author(s):  
D. T. ALFONSO ◽  
A. SOTREL ◽  
J. A. I. Grossman

We report a 2-year-old girl with carpal tunnel syndrome due to a large intraneural perineurioma that required resection and nerve reconstruction.


2006 ◽  
Vol 104 (5) ◽  
pp. 824-827 ◽  
Author(s):  
Rami Almefty ◽  
Bruce L. Webber ◽  
Kenan I. Arnautović

✓Intraneural perineurioma is a true but rare neoplasm that originates from perineurial cells and mainly affects peripheral nerves. It must be distinguished from other hypertrophic neuropathies that are either inflammatory or demonstrate an onion-bulb formation that originates from Schwann cells. Complying with this strict definition, only three additional cases of cranium-related perineurioma have been identified: two lesions arose extracranially and involved cranial nerves, and one occurred intracranially but did not involve a nerve. The authors describe a 27-year-old woman who presented with left third cranial nerve palsy and was found to harbor a mass lesion in the superior orbital fissure and cavernous sinus. After subtotal resection had been performed, pathological studies confirmed the presence of perineurial tumor cells in a pseudo–onion bulb formation. The cells stained positively for epithelial membrane antigen but not for S100 protein, clearly distinguishing the disease from one that originates in Schwann cells.


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