Evidence map›Paper›PMID 41878779›Full record

ArticleNephrology (Carlton, Vic.)2026

Rapidly Progressive Kidney Failure With Transient Non-Cystic Kidney Enlargement: A Case Report Highlighting Delayed Medullary Cyst Formation.

Hiroki Ito, Shigeto Mashiko, Shinichi Mizuno, Yoshitaka Kanomata, Kentaro Yano, Yuya Suzuki, Fumiya Sato, Ryo Tajima, Go Anan, Takuo Hirose and 2 more

Abstract readCase Reports
In one paragraph

Article in Nephrology (Carlton, Vic.), 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

12 authors.

Hiroki ItoDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.ORCID https://orcid.org/0000-0003-1239-6551
Shigeto MashikoDivision of Geriatric and Community Medicine, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Shinichi MizunoDepartment of Nephrology, Japan Community Health Care Organization Sendai Hospital, Sendai, Japan.
Yoshitaka KanomataDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Kentaro YanoDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Yuya SuzukiDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Fumiya SatoDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Ryo TajimaDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Go AnanDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Takuo HiroseDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Katsuya IshiyamaDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Takefumi MoriDivision of Nephrology and Hypertension, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary tubulointerstitial kidney diseases typically manifest as slowly progressive chronic kidney disease. Rapidly progressive kidney failure with non-cystic nephromegaly is an exceptionally rare presentation posing significant diagnostic challenges. We describe a 64-year-old man presenting with rapidly progressive kidney failure and bilateral non-cystic kidney enlargement. Initial imaging, including computed tomography (CT) and magnetic resonance imaging (MRI), revealed no cysts. Kidney biopsy showed tubular ectasia and basement membrane abnormalities consistent with tubulointerstitial disease, and genetic analysis identified a heterozygous NPHP1 variant. Although liver biopsy supported a diagnosis of nephronophthisis-related ciliopathy, the aggressive clinical course and absence of cysts were atypical. Notably, 5 years after initiating haemodialysis, follow-up MRI revealed numerous medullary cysts that were previously undetectable. Crucially, these cysts were clearly visible on MRI but remained indistinguishable on concurrent CT. This case illustrates a deceptive 'pre-cystic' phase characterised by rapid progression and inflammatory nephromegaly. It underscores that initial cyst absence does not exclude the diagnosis and establishes the critical superiority of MRI over CT for detecting delayed medullary cysts to determine the aetiology in end-stage kidneys.

Indexed as

Kidney Diseases, CysticKidney Failure, ChronicRenal InsufficiencyAdaptor Proteins, Signal TransducingBiopsyCytoskeletal ProteinsDisease ProgressionGenetic Predisposition to DiseaseHumansMagnetic Resonance ImagingMaleMembrane ProteinsMiddle AgedPhenotypeTime FactorsTomography, X-Ray ComputedAdaptor Proteins, Signal TransducingCytoskeletal ProteinsMembrane ProteinsNPHP1 protein, humanADTKDMCKDmedullary cystNPHP‐RC

Identifiers

PMID41878779
PMCPMC13014208

What OpenQuestion holds

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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.