Evidence map›Paper›PMID 42518687›Full record

ArticleRespirology case reports2026

Anomalous Systemic Arterial Supply to the Basal Segment of the Lung Treated With Surgery Versus Transcatheter Embolisation: A Report of Two Cases.

Hidenori Takahashi, Shinichiro Ota, Yugo Satake, Hiroki Nagamatsu, Ryutaro Hirose, Mio Toyama-Kosaka, Miwa Morikawa, Takashi Makino, Yuta Tajiri, Natsuko Nakano and 1 more

Abstract read
In one paragraph

Article in Respirology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Hidenori TakahashiRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.ORCID https://orcid.org/0000-0001-9781-258X
Shinichiro OtaRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Yugo SatakeRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Hiroki NagamatsuRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Ryutaro HiroseRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Mio Toyama-KosakaRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Miwa MorikawaRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Takashi MakinoRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.
Yuta TajiriDepartment of Cardiovascular Medicine Tokyo Shinagawa Hospital Tokyo Japan.
Natsuko NakanoDepartment of Pathology Tokyo Shinagawa Hospital Tokyo Japan.
Masaharu ShinkaiRespiratory Disease Center Tokyo Shinagawa Hospital Tokyo Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anomalous systemic arterial supply to the basal segment of the lungs (ABLL) is a rare congenital vascular anomaly, and its treatment remains disputed. We report two cases of ABLL that were asymptomatic and managed using different strategies based on infection status and anatomical complexity. A 25-year-old woman presented with a right lower lobe cavitary lesion supplied by an anomalous coeliac artery branch. Due to suspected chronic fungal infection, thoracoscopic right basal segmentectomy was performed, and subsequent pathology and cultures confirmed chronic cavitary aspergillosis. A 33-year-old man presented with an anomalous branch from the descending thoracic aorta supplying the left basal segment. Surgical resection was considered potentially more invasive because of an incomplete fissure and a common left pulmonary vein trunk; therefore, transcatheter embolisation was successfully performed. These cases suggest that treatment selection should be individualised and guided not only by vessel diameter but also by associated infection and anatomical complexity.

Indexed as

anomalous systemic arterial supply to the basal segment of the lungaspergillosiscavitary lesionembolisationsegmentectomy

Identifiers

PMID42518687
PMCPMC13381719

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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.