Literature DB >> 23744601

Asymmetric sensory ganglionopathy: a case series.

Celedonio Marquez-Infante1, Sinéad M Murphy, Liberty Mathew, Ali Alsanousi, Michael P Lunn, Sebastian Brandner, Tarek A Yousry, Julian Blake, Mary M Reilly.   

Abstract

INTRODUCTION: Sensory ganglionopathies are uncommon but potentially very disabling. They have heterogeneous etiologies including autoimmune, paraneoplastic, toxic, and inflammatory although many remain idiopathic despite intensive investigation. Asymmetric sensory loss is relatively common at the onset, but with time, symptoms usually spread to involve all limbs symmetrically.
METHODS: We report 6 patients with a persistent strikingly asymmetrical sensory ganglionopathy with acute or subacute onset and slow progression.
RESULTS: Peripheral nerve biopsies in 5 patients showed axonal loss without significant inflammation; a dorsal root ganglion biopsy in 1 patient showed neuronal loss and inflammatory infiltrate. Four patients received immunomodulatory treatment, but overall the response to treatment was poor.
CONCLUSIONS: Asymmetrical sensory ganglionopathies may have an inflammatory basis. Immunomodulatory therapy may be considered early in the disease course, although in this series there was a limited response to treatment.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23744601     DOI: 10.1002/mus.23772

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  3 in total

Review 1.  Chronic idiopathic axonal polyneuropathy: a systematic review.

Authors:  Panagiotis Zis; Ptolemaios Georgios Sarrigiannis; Dasappaiah Ganesh Rao; Channa Hewamadduma; Marios Hadjivassiliou
Journal:  J Neurol       Date:  2016-03-09       Impact factor: 4.849

2.  Sensory neuronopathy associated with cholangiocarcinoma diagnosed 6 years after symptom onset.

Authors:  Alexander M Rossor; Julian Blake; Theodora Pissanou; Mary M Reilly
Journal:  BMJ Case Rep       Date:  2017-12-20

3.  TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMN.

Authors:  Alexander M Rossor; Zane Jaunmuktane; Martin N Rossor; Glen Hoti; Mary M Reilly
Journal:  Neurology       Date:  2019-01-30       Impact factor: 9.910

  3 in total

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