Evidence map›Paper›PMID 39866275›Full record

ArticleAME case reports2025

Myeloperoxidase anti-neutrophil cytoplasmic antibody-associated vasculitis with silicosis, alveolar hemorrhage, and rapidly progressive glomerulonephritis: a case report.

Keiichi Mizuhashi

Abstract readCase Reports
In one paragraph

Article in AME case reports, 2025. 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

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.

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

1 author.

Keiichi MizuhashiCenter for Asbestos-Related Diseases, Toyama Rosai Hospital, Toyama, Japan.ORCID https://orcid.org/0000-0003-0709-5041

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The underlying pathophysiology of some occupational diseases such as silicosis involves autoantibodies. An autoantibody, antineutrophil cytoplasmic antibody (ANCA), has been recently reported and is known to be elevated in diseases such as vasculitis; therefore, the disease is currently known as ANCA-associated vasculitis. The risk of ANCA-associated vasculitis is known to be 25 times higher in patients with silicosis than in those without any occupational disease. In this report, the author describes the case of a man who developed ANCA-associated vasculitis after silicosis, leading to severe alveolar hemorrhage and renal dysfunction. Case Description: A Japanese man in his 50s who was engaged in tunnel construction for 33 years presented with the chief complaint of cough with sputum. Based on chest images and his occupational history, a diagnosis of silicosis was made. In November 2008, urinary occult blood was detected; therefore, myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA) levels were measured (15.9 U/mL). In September 2009, he experienced systemic fatigue, fever, night sweats, bloody sputum, and difficulty breathing. Chest images showed new shadows, and MPO-ANCA levels had increased to 690 U/mL. His bronchoalveolar lavage fluid was bloody, confirming alveolar hemorrhage. The bloody sputum resolved spontaneously; however, a subsequent short-term increase in serum creatinine levels was observed. Renal biopsy confirmed necrotizing crescentic glomerulonephritis. Therefore, he was diagnosed with MPO-ANCA-associated vasculitis with silicosis, alveolar hemorrhage, and rapidly progressive glomerulonephritis. Treatment with combination therapy of pulse methylprednisolone sodium succinate and cyclophosphamide led to remission. Conclusions: For patients with silicosis, accompanied by bloody sputum or other symptoms, ANCA-associated vasculitis, besides tuberculosis and lung cancer, should be considered. It is also necessary to pay close attention to the possible onset of rapidly progressive glomerulonephritis because it is sometimes fatal. In addition, when examining a patient with rapidly progressive glomerulonephritis, attention must be paid to whether the patient has had previous exposure to silica dust, regardless of whether or not the exposure was occupational.

Indexed as

alveolar hemorrhageantineutrophil cytoplasmic antibody-associated vasculitis (ANCA-associated vasculitis)case reportrapidly progressive glomerulonephritisSilicosis

Identifiers

PMID39866275
PMCPMC11760511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.