Evidence map›Paper›PMID 41676791›Full record

ArticleJMA journal2026

Eosinophilic Granulomatosis with Polyangiitis Presenting with Intermittent Claudication.

Koichi Bamba, Daisuke Fujishiro, Tomoki Kawahata, Yuki Kamikokura, Tsubasa Ono, Yuta Ikechi, Kitaru Tanaka, Kensaku Okamoto, Yuichi Makino, Hiroshi Nomoto

Abstract readCase Reports
In one paragraph

Article in JMA journal, 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

10 authors.

Koichi BambaDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Daisuke FujishiroDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Tomoki KawahataDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Yuki KamikokuraDepartment of Diagnostic Pathology, Asahikawa Medical University Hospital, Asahikawa, Japan.
Tsubasa OnoDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Yuta IkechiDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Kitaru TanakaDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Kensaku OkamotoDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.
Yuichi MakinoCenter for Medical Education and Regional Symbiosis, Asahikawa Medical University, Asahikawa, Japan.
Hiroshi NomotoDivision of Endocrinology, Metabolism, and Rheumatology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intermittent claudication (IC), characterized by lower limb weakness and pain during walking that resolves with rest, is most commonly caused by lumbar spinal canal stenosis or peripheral arterial disease. We report a unique case of eosinophilic granulomatosis with polyangiitis (EGPA) presenting with IC. An 80-year-old woman presented with fever, muscle pain, muscle weakness, and IC. She had a history of bronchial asthma and allergic rhinitis. Laboratory tests revealed eosinophilia (4,212 /μL) and elevated creatine kinase levels (505 U/L). Magnetic resonance imaging (MRI) with short tau inversion recovery sequences demonstrated diffuse high-signal intensity across multiple skeletal muscles. A biopsy specimen of the right biceps brachii, taken from a high-signal area identified on MRI, showed inflammatory cell infiltration, primarily composed of eosinophils and lymphocytes in the blood vessel walls. The patient was diagnosed with EGPA-associated skeletal muscle involvement and treated with a moderate dose of glucocorticoids, resulting in significant clinical improvement. This case highlights that EGPA can present with IC, a rare manifestation of the disease, and underscores the diagnostic value of MRI in such cases. MRI may be a useful tool for localizing biopsy sites in patients with EGPA-related muscle damage. Clinicians should consider anti-neutrophil cytoplasmic antibody-associated vasculitis, including EGPA, in patients presenting with IC and systemic symptoms, and initiate early diagnostic and therapeutic interventions.

Indexed as

anti-neutrophil cytoplasmic antibody-associated vasculitiscreatine kinaseeosinophilic granulomatosis with polyangiitisintermittent claudicationmagnetic resonance imagingmuscle pain

Identifiers

PMID41676791
PMCPMC12889226

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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.