Evidence map›Paper›PMID 40707229›Full record

ArticleInternal medicine (Tokyo, Japan)2026

Microscopic Polyangiitis Initially Suspected of Being Anti-synthetase Syndrome.

Tomoo Tsujihata, Hirofumi Miyake, Eri Iwai-Kanai, Shinji Sumiyoshi, Takeshi Kubo, Ichizo Nishino, Kazuhiro Hatta

Abstract readCase Reports
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2026. 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
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

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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.

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

7 authors.

Tomoo TsujihataDepartment of General Internal Medicine, Tenri Hospital, Japan.
Hirofumi MiyakeDepartment of General Internal Medicine, Tenri Hospital, Japan.
Eri Iwai-KanaiDepartment of General Internal Medicine, Tenri Hospital, Japan.
Shinji SumiyoshiDepartment of Diagnostic Pathology, Tenri Hospital, Japan.
Takeshi KuboDepartment of Radiology, Tenri Hospital, Japan.
Ichizo NishinoDepartment of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Japan.
Kazuhiro HattaDepartment of General Internal Medicine, Tenri Hospital, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-synthetase syndrome is an autoimmune disorder associated with anti-aminoacyl-tRNA synthetase antibodies, including anti-Jo-1. However, antibody positivity alone is insufficient for the diagnosis because overlapping features with other diseases may lead to a misdiagnosis. We herein report a 69-year-old woman initially suspected of having anti-synthetase syndrome due to anti-Jo-1 antibody positivity and muscle weakness. Additional findings, including mononeuritis multiplex, purpura, crescentic glomerulonephritis, and strongly positive myeloperoxidase-antineutrophil cytoplasmic antibodies, led to a diagnosis of microscopic polyangiitis. Although anti-Jo-1 antibodies are highly specific, false-positive results can occur. This case highlights the need for a comprehensive evaluation beyond antibody testing to avoid diagnostic errors.

Indexed as

Amino Acyl-tRNA SynthetasesAutoimmune DiseasesMicroscopic PolyangiitisAgedAntibodies, Antineutrophil CytoplasmicAntibodies, AntinuclearDiagnosis, DifferentialDiagnostic ErrorsFemaleHumansMyositisAmino Acyl-tRNA SynthetasesAntibodies, Antineutrophil CytoplasmicAntibodies, AntinuclearJo-1 antibodyanti-Jo-1 antibodyanti-synthetase syndromeinterstitial lung diseasemicroscopic polyangiitismononeuritis multiplex

Identifiers

PMID40707229
PMCPMC12979714

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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.