Evidence map›Paper›PMID 41900925›Full record

ArticleLife (Basel, Switzerland)2026

Rare Association of Bilateral Central Salzmann Nodular Degeneration and Fuchs Endothelial Dystrophy Managed by DMEK: A Case Report.

Alina Gabriela Gheorghe, Ana Maria Arghirescu, Maria Cristina Marinescu, Doina Mihaela Pop, Liliana Mary Voinea, Radu Ciuluvică

Abstract readCase Reports
In one paragraph

Article in Life (Basel, Switzerland), 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

6 authors.

Alina Gabriela GheorgheDepartment of Ophthalmology, Clinical Institute of Ophthalmological Emergencies "Prof. Dr. Mircea Olteanu", 010464 Bucharest, Romania.ORCID 0000-0002-9700-6112
Ana Maria ArghirescuDepartment of Ophthalmology, Clinical Institute of Ophthalmological Emergencies "Prof. Dr. Mircea Olteanu", 010464 Bucharest, Romania.ORCID 0009-0008-4802-1472
Maria Cristina MarinescuDoctoral School, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.ORCID 0000-0001-8242-8809
Doina Mihaela PopFoisor Orthopaedic Hospital, 030167 Bucharest, Romania.
Liliana Mary VoineaDoctoral School, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.
Radu CiuluvicăDepartment of Anatomy, Faculty of Dental Medicine, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Salzmann nodular degeneration is a slowly progressive, rare, degenerative disease of the cornea, usually associated with other ocular pathologies such as dry eye disease, previous ocular surgery, involving the peripheral cornea. We present the surgical management of a rare case of a patient diagnosed with Fuchs endothelial dystrophy where the Salzmann nodules present an unusual bilateral central corneal involvement and overlap the area with the most pronounced endothelial dysfunction. The patient underwent anterior superficial keratectomy, cataract surgery and Descemet membrane endothelial keratoplasty (DMEK). In vivo confocal microscopy and anterior segment optical coherence tomography have been used to monitor the morphological and structural evolution.

Indexed as

anterior segment optical coherence tomographycorneal transplantDMEKin vivo confocal microscopySalzmann corneal degenerationSalzmann nodular degeneration

Identifiers

PMID41900925
PMCPMC13028125

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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.