Evidence map›Paper›PMID 40951054›Full record

ArticleCureus2025

Eyelid Amyloidosis: A Rare Condition With Diagnostic Challenges.

Omar Alobaidan, Naif Al Sulaiman, Abeer Alharbi, Nouf Almushayt

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

4 authors.

Omar AlobaidanOculoplastics, King Khaled Eye Specialist Hospital, Riyadh, SAU.
Naif Al SulaimanOculoplastics, King Khaled Eye Specialist Hospital, Riyadh, SAU.
Abeer AlharbiOphthalmology, Ohud Hospital, Medina, SAU.
Nouf AlmushaytOphthalmology, Abha Maternity and Children Hospital, Abha, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a rare and challenging case of a man who presented with mild mechanical ptosis and inferior dystopia, diagnosed with eyelid amyloidosis. A 40-year-old healthy man presented with a painless mass on his left upper eyelid that started one year ago. He noted that the mass increases in size when he eats meat, but there has been no overall progression over time. He experienced inferior dystopia with left upper eyelid fullness, swelling, and mild mechanical ptosis of the left eye. The measurements were as follows: marginal reflex distance 1 was 5 mm (oculus dexter, OD) and 4 mm (oculus sinister, OS); palpebral fissure height was 13 mm (OD) and 10 mm (OS); Hertel exophthalmometer reading at 105 was 22 mm (OD) and 23 mm (OS). CT was done with the impression of a dermoid cyst. It showed complex mass lesions of mixed fat, soft tissue, and calcification, predominantly involving the left upper eyelid with deeper extension into the superior compartment of the extraconal part of the fat of the orbit, close to the superior oblique levator muscle, with subsequent mild enlargement of the extraconal muscle group bilaterally, predominantly seen on the left side. The excisional biopsy showed amyloidosis. Amyloidosis is uncommon, progressive, and slowly associated with significant ocular morbidity. The diagnosis might be delayed because of an unusual presentation.

Indexed as

dystopialid swellingmeibomian gland atrophyptosissystemic amyloidosis

Identifiers

PMID40951054
PMCPMC12433314

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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.