Evidence map›Paper›PMID 40670097›Full record

ArticleInternal medicine (Tokyo, Japan)2026

Hepatic Cyst Infection in a Hemodialysis Patient with Autosomal Dominant Polycystic Kidney Disease Complicated by Non-symptomatic Caroli Disease.

Ayaka Hane, Tatsuya Suwabe, Yuki Oba, Shigekazu Kurihara, Hiroki Mizuno, Hisashi Kamido, Hisashi Sugimoto, Noriko Inoue, Akinari Sekine, Masayuki Yamanouchi and 7 more

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

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

17 authors.

Ayaka HaneNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Tatsuya SuwabeNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Yuki ObaNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Shigekazu KuriharaNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Hiroki MizunoNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Hisashi KamidoNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Hisashi SugimotoNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Noriko InoueNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Akinari SekineNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Masayuki YamanouchiNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Kiho TanakaNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Eiko HasegawaNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Takehiko WadaNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Naoya MorisadaDepartment of Pediatrics, Kobe University Graduate School of Medicine, Japan.
Kandai NozuDepartment of Pediatrics, Kobe University Graduate School of Medicine, Japan.
Naoki SawaNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.
Yoshifumi UbaraNephrology Center and the Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An 84-year-old woman undergoing hemodialysis for autosomal dominant polycystic kidney disease (ADPKD) was admitted for refractory hepatic cyst infection. Magnetic resonance cholangiopancreatography and contrast-enhanced computed tomography revealed a concurrent complication of Caroli disease, diagnosed by cystic dilatation of the intrahepatic bile duct and a central dot sign in the vicinity of the infected liver cyst. However, there was no traffic between the infected liver cyst and dilated bile duct, and the cyst drainage procedure was curative. In cases where both diseases were combined, it was suggested that two infections, cyst and biliary tract infections, could occur.

Indexed as

Caroli DiseaseCystsLiver DiseasesPolycystic Kidney, Autosomal DominantRenal DialysisAged, 80 and overFemaleHumansautosomal dominant polycystic kidney diseasenon-symptomatic Caroli diseaserecurrent hepatic cyst infection

Identifiers

PMID40670097
PMCPMC12945427

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Registered trials

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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.