Evidence map›Paper›PMID 40952581›Full record

ArticleCEN case reports2025

A case of kidney disease related to Staphylococcus epidermidis infection soon after insertion of a central venous catheter.

Kei Kono, Naoki Sawa, Daisuke Ikuma, Yuki Oba, Hiroki Mizuno, Akinari Sekine, Noriko Inoue, Kiho Tanaka, Masayuki Yamanouchi, Eiko Hasegawa and 7 more

Erratum issuedAbstract readCase Reports
In one paragraph

Article in CEN case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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

5 · Who and what money

Authors and funding

17 authors.

Kei KonoDepartment of Pathology, Toranomon Hospital, Tokyo, Japan.
Naoki SawaNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Daisuke IkumaNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Yuki ObaNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Hiroki MizunoNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Akinari SekineNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Noriko InoueNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Kiho TanakaNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Masayuki YamanouchiNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Eiko HasegawaNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Tatsuya SuwabeNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Takeshi FujiiDepartment of Pathology, Toranomon Hospital, Tokyo, Japan.
Yutaka TakazawaDepartment of Pathology, Toranomon Hospital, Tokyo, Japan.
Kenichi OhashiDepartment of Pathology, Toranomon Hospital, Tokyo, Japan.
Yutaka YamaguchiYamaguchi's Pathology Laboratory, Chiba, Japan.
Takehiko WadaNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan.
Yoshifumi UbaraNephrology Center, The Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Kajigaya, 1-3-1, Takatsu, Kawasaki, Tokyo, Kanagawa, 212-0015, Japan. ubara@toranomon.gr.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Central venous catheter (CVC)-related kidney disease has been well documented in cases of long-term catheter use, typically manifesting as membranoproliferative glomerulonephritis with immunoglobulin (Ig)M and C3 deposits after months to years of catheterization. We report an exceptional case of rapidly progressive kidney disease that developed just 7 days after CVC insertion in a 74-year-old man who underwent laparoscopic rectal cancer surgery. The patient presented with high fever (39 ℃) and acute kidney injury, with serum creatinine rapidly escalating from a baseline of 1.1-2.7 mg/dL. Laboratory evaluation revealed marked hypocomplementemia (C3 35 mg/dL, C4 5 mg/dL), significant proteinuria (1.5 g/day), and hematuria. Catheter tip culture isolated multidrug-resistant Staphylococcus epidermidis. Kidney biopsy demonstrated distinctive pathological findings characterized by endocapillary proliferative glomerulonephritis with massive fibrin deposition, confirmed by phosphotungstic acid-hematoxylin (PTAH) staining. Immunofluorescence revealed granular deposits of IgG and C3 along the capillary wall, notably without IgA or IgM deposits. Electron microscopy identified characteristic fibrin deposits measuring 7-8 nm in thickness, predominantly in the subendothelial region. DnaJ homolog subfamily B member 9 (DNAJB9) staining was negative, definitively excluding fibrillary glomerulonephritis (FGN). Following catheter removal and targeted antibiotic therapy without steroid treatment, the patient's renal function showed remarkable improvement, with creatinine decreasing to 1.8 mg/dL at discharge and further improving to 1.0 mg/dL after 1 year. This case demonstrates that S. epidermidis can induce severe glomerular lesions through fibrin deposition within an extraordinarily short timeframe, contrasting dramatically with the immune complex-mediated injury typically observed in long-term CVC use.

Indexed as

Acute Kidney InjuryCatheterization, Central VenousCatheter-Related InfectionsCentral Venous CathetersStaphylococcal InfectionsStaphylococcus epidermidisAgedAnti-Bacterial AgentsGlomerulonephritis, MembranoproliferativeHumansKidneyMaleAnti-Bacterial AgentsCentral venous catheter-related kidney diseaseEndocapillary glomerulonephritis with massive fibrin depositionStaphylococcus epidermidis

Identifiers

PMID40952581
PMCPMC12605852

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