Evidence map›Paper›PMID 30843116›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2019

Cancer and motor neuron disease-causal or coincidental? Two contrasting cases.

John Goodfellow, George Gorrie, Veronica Leach, Sameer Patel, Graham Mackay

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Anti-Hu associated paraneoplastic upper and lower motor neuropathy triggered by atezolizumab.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  3. Article
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

5 authors at 3 institutions in 1 country.

John GoodfellowNeuroimmunology Laboratory, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, G51 4TF, UK.
George GorrieDepartment of Neurology, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, G51 4TF, UK.
Veronica LeachDepartment of Neurophysiology, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, G51 4TF, UK.
Sameer PatelDepartment of Respiratory Medicine, Hairmyres Hospital, Eaglesham Road, East Kilbride, G75 8RG, UK.
Graham MackayDepartment of Neurology, Aberdeen Royal Infirmary, Foresterhill Road, Aberdeen, AB25 2ZN, UK. grahammackay@doctors.org.uk.ORCID http://orcid.org/0000-0002-4316-2320
Queen Elizabeth University Hospital · GBAberdeen Royal Infirmary · GBHairmyres Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMotor neuron disease (MND) can occur in patients with cancer, but there is minimal evidence that this is more than by chance. We contrast two cases of motor neuronopathies occurring in the context of systemic malignancy and argue that in one case the cause was most likely paraneoplastic, while in the other it was not. CASE 1: A 61-year-old woman developed progressive walking difficulties over 9 months with weakness and stiffness in her legs. EMG showed fibrillations and positive sharp waves in multiple lower limb muscles bilaterally, with neurogenic units and a reduced recruitment pattern. An invasive ductal carcinoma of the breast was identified and she continued to deteriorate neurologically with worsening mobility, upper limb spasticity and fasciculations. She died approximately 26 months after symptom onset. CASE 2: A 57-year-old woman developed weight loss and weakness of her right arm without any sensory symptoms. At presentation, she had wasting and fasciculations in her right upper limb muscles, with normal reflexes, normal left upper limb and lower limb examination. Over the following week, she developed left upper limb weakness and fasciculations, brisk knee reflexes, and flexor plantar responses. Her EMG showed upper and lower limb denervation. She was found to have anti-Hu and anti-CV2 antibodies present in serum. A PET-CT showed active uptake in lymph nodes in the right hilum. Biopsy confirmed a small cell lung cancer. She had chemoradiation therapy and the tumour went into remission. She has remained well on follow-up 24 months later, regaining weight and strength after her chemotherapy. She continues to be monitored for cancer recurrence, but thus far appears to be in remission.

conclusionIn cases with rapidly progressive MND, particularly of upper limb onset, consideration should be given to testing anti-neuronal antibodies and searching for an occult tumour.

Indexed as

Paraneoplastic Syndromes, Nervous SystemBreast NeoplasmsCarcinoma, Ductal, BreastFatal OutcomeFemaleHumansLung NeoplasmsMiddle AgedMotor Neuron DiseaseSmall Cell Lung CarcinomaAmyotrophic lateral sclerosisCancerLower motor neurone signsMotor neuron diseaseParaneoplasticUpper motor neurone signs

Identifiers

PMID30843116
OpenAlexW2921477232

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.