Evidence map›Paper›PMID 38390536›Full record

ArticleIndian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India

Autoimmune Encephalitis as a Rare Paraneoplastic Syndrome in Adrenocortical Carcinoma.

Debabrata Mohapatra, Madhavi Tripathi, Sakshi Ojha, Jagdish Prasad Meena, Biswaroop Chakrabarty

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 64% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 2 countries.

Debabrata MohapatraDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Madhavi TripathiDepartment of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.
Sakshi OjhaDepartment of Pediatrics, Division of Pediatric Neurology, All India Institute of Medical Sciences, New Delhi, India.
Jagdish Prasad MeenaDepartment of Pediatrics, Division of Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
Biswaroop ChakrabartyDepartment of Pediatrics, Division of Pediatric Neurology, All India Institute of Medical Sciences, New Delhi, India.
Creative Commons · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paraneoplastic neurologic syndromes (PNSs) are rare in pediatrics and are understood to be consequences of cross-reactivity against various neuroendocrine antigens expressed on cancer cells. Here, we report a case of autoimmune encephalitis, a type of PNS associated with a case of adrenocortical carcinoma (ACC), that had a clinical response to immunosuppressive therapy. ACC is a rare tumor with controversial tissue of origin but expresses various neuroendocrine antigens that could be the possible mechanism for this rare yet interesting association.

Indexed as

Adrenocortical carcinomaparaneoplastic neurological syndromeseronegative autoimmune encephalitis

Identifiers

PMID38390536
PMCPMC10880859
OpenAlexW4390055302

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.