Evidence map›Paper›PMID 36415783›Full record

ArticleRespirology case reports2022

Pulmonary sarcoidosis with a cavitary lesion in the lung caused by a TNF-α inhibitor: A case report.

Eriko Hamada, Yoshifumi Yamamoto, Yosuke Okuda, Kazuhiro Sakaguchi, Kentaro Suzuki, Yoshiro Kai, Maiko Takeda, Shigeto Hontsu, Motoo Yamauchi, Masanori Yoshikawa and 3 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Respirology case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Overview of multi-omics approaches for pulmonary sarcoidosis.EC pulmonology and respiratory medicine · 2025
    Article
  6. Review
  7. Article
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

13 authors at 3 institutions in 2 countries.

Eriko HamadaDepartment of Respiratory Medicine Nara Medical University Nara Japan.ORCID https://orcid.org/0000-0003-0913-2475
Yoshifumi YamamotoDepartment of Respiratory Medicine Nara Medical University Nara Japan.
Yosuke OkudaDepartment of Respiratory Medicine Nara Medical University Nara Japan.
Kazuhiro SakaguchiDepartment of Respiratory Medicine Nara Medical University Nara Japan.
Kentaro SuzukiDepartment of Respiratory Medicine Minami-Nara General Medical Center Nara Japan.
Yoshiro KaiDepartment of Respiratory Medicine Minami-Nara General Medical Center Nara Japan.ORCID https://orcid.org/0000-0001-6197-5176
Maiko TakedaDepartment of Diagnostic Pathology Nara Medical University Nara Japan.
Shigeto HontsuDepartment of Respiratory Medicine Nara Medical University Nara Japan.
Motoo YamauchiDepartment of Respiratory Medicine Nara Medical University Nara Japan.ORCID https://orcid.org/0000-0003-1754-703X
Masanori YoshikawaDepartment of Respiratory Medicine Nara Medical University Nara Japan.
Noriyoshi SawabataDepartment of Thoracic and Cardiovascular Surgery Nara Medical University Nara Japan.ORCID https://orcid.org/0000-0002-4899-1005
Chiho OhbayashiDepartment of Diagnostic Pathology Nara Medical University Nara Japan.ORCID https://orcid.org/0000-0002-8046-9508
Shigeo MuroDepartment of Respiratory Medicine Nara Medical University Nara Japan.ORCID https://orcid.org/0000-0001-7452-9191
Nara Medical University Hospital · JPNara Medical University · JPNational Archives and Records Administration · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 28-year-old man with ankylosing spondylitis (AS) who was treated with a tumour necrosis factor-alpha (TNF-α) inhibitor, adalimumab, presented with newly detected multiple bilateral pulmonary nodules on chest computed tomography (CT). We suspected bacterial infection, including those caused by acid-fast bacilli, or adalimumab-related condition, such as sarcoidosis. After adalimumab cessation, no resolution of the pulmonary shadows was observed. Moreover, pulmonary cavitation appeared on chest CT at 7 weeks, prompting surgical lung biopsy. Acid-fast bacteria culture of the lung tissue showed negative results. Pathological examination suggested that confluent granulomas associated with sarcoidosis might have obstructed the blood vessels, causing necrosis and lung cavitation. Consequently, prednisolone was initiated, and these shadows were reduced. After administering anti-interleukin (IL)-17A antibody for treatment of AS and prednisolone withdrawal, these shadows were not exacerbated. TNF-α inhibitor-induced sarcoidosis could cause cavitary lesions due to vascular invasion of granulomas.

Indexed as

adalimumabankylosing spondylitisinterleukin‐17sarcoidosistumour necrosis factor‐alpha

Identifiers

PMID36415783
PMCPMC9673597
OpenAlexW4309377607

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.