Evidence map›Paper›PMID 27603395›Full record

ArticleMedicine2016

Monoclonal gammopathy of undeterminated significance and endoneurial IgG deposition: A case report.

Stéphane Mathis, Jérôme Franques, Laurence Richard, Jean-Michel Vallat

Abstract readCase Reports
In one paragraph

Article in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Review
  3. The ataxic neuropathies.Journal of neurology · 2021
    Review
  4. Review
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Stéphane MathisDepartment of Neurology, Nerve-Muscle Unit, CHU Bordeaux (Groupe hospitalier Pellegrin), Place Amélie Raba-Léon, Bordeaux, France La Casamance Hospital, Aubagne, France European Hospital, Marseille, France Department and Laboratory of Neurology, Centre de Référence 'neuropathies périphériques rares', CHU Limoges, Limoges, France.
Jérôme Franques
Laurence Richard
Jean-Michel Vallat

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMonoclonal gammopathy of undeterminated significance is the most common form of plasma cell dyscrasia, usually considered as benign. In rare cases it may have a malignant course, sometimes limited to an organ such as peripheral nerves.

methodsWe describe clinical, electrophysiological and pathological findings in a patient presenting a immunoglobulin G (IgG) paraproteinemic polyneuropathy clinically mimicking a chronic inflammatory demyelinating polyneuropathy.

resultsImmuno-electron microscopy (immune-EM) demonstrated that the widenings of the myelin lamellae resulted from the infiltration of IgG between a significant number of myelin lamellae (with absence of inflammatory cells in the epineurium, endoneurium, and perineurium, and the lack signs of vasculitis). This patient was finally treated successfully with lenalidomide then mycophenolate mofetil.

conclusionsIn polyneuropathies associated to a monoclonal gammopathy, a nerve biopsy may clinch the diagnosis. Immuno-EM may be required to determine the role of the pathological immunoglobulin in the destruction of the peripheral nerve parenchyma. Diagnosis of such a direct involvement of peripheral nerve can endorse more aggressive treatment of real efficiency.

Indexed as

HumansImmunoglobulin GMaleMiddle AgedMonoclonal Gammopathy of Undetermined SignificancePeripheral NervesPolyradiculoneuropathy, Chronic Inflammatory DemyelinatingImmunoglobulin G

Identifiers

PMID27603395
PMCPMC5023918

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