Evidence map›Paper›PMID 38874737›Full record

ArticleCerebellum (London, England)2024

Plasmapheresis and IVIG for Treatment of Non-Tumor Anti-Tr/DNER Antibody-Associated Ataxia: A Case Report.

Armin Adibi, Ali Rastegar-Kashkouli, Pourya Yousefi, Iman Adibi, Elahe Ahmadi, Saba Naghavi

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In one paragraph

Article in Cerebellum (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Armin AdibiNeuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Ali Rastegar-KashkouliNeuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Pourya YousefiNeuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Iman AdibiNeuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran. i.adibi@gmail.com.
Elahe AhmadiNeuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Saba NaghaviNeuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune cerebellar ataxia (ACA) is a condition characterized by progressive ataxia resulting from an immune-mediated attack on cerebellar structures. The presence of anti-Tr/DNER antibodies, strongly associated with Hodgkin lymphoma, has been identified in ACA. However, cases with no underlying malignancy are rare. We report the case of a 49-year-old woman presenting with progressive ataxia, slurred speech, and dizziness over three months. The patient exhibited significant cerebellar symptoms, including dysarthria and limb ataxia, without signs of other systemic illnesses. Comprehensive investigations, including imaging, lumbar puncture, and autoantibody testing, were performed. The cerebrospinal fluid (CSF) sample revealed positivity for Tr/DNER antibodies, leading to a diagnosis of autoimmune cerebellar ataxia. The patient underwent nine sessions of plasmapheresis, followed by six doses of intravenous immunoglobulin (IVIG), resulting in significant clinical improvement. Despite extensive cancer screening, no underlying malignancy was detected, suggesting a non-tumor origin of anti-Tr/DNER antibodies. The patient's gait improved, ataxia resolved, and cerebellar tests normalized following treatment. The patient was further managed with rituximab treatment every six months. This case represents a presentation of anti-Tr/DNER-associated autoimmune cerebellar ataxia without malignancy. The successful treatment with plasmapheresis and IVIG suggests that these interventions may be effective in managing autoimmune cerebellar ataxia associated with anti-Tr/DNER antibodies. Further research is needed to understand the underlying mechanisms of this condition and to determine the optimal treatment strategies.

Indexed as

AutoantibodiesCerebellar AtaxiaImmunoglobulins, IntravenousPlasmapheresisFemaleHumansMiddle AgedAutoantibodiesImmunoglobulins, IntravenousAutoantibodiesAutoimmune cerebellar ataxiaCase reportCentral nervous systemDelta/notch-like epidermal growth

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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.