Evidence map›Paper›PMID 39469422›Full record

ArticleAmerican journal of ophthalmology case reports2024

Bilateral asynchronous acute idiopathic maculopathy with disease recurrence.

Yichen Fan, Zachary A Kroeger, Christina J Flaxel

Abstract readCase Reports
In one paragraph

Article in American journal of ophthalmology case reports, 2024. 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

3 authors.

Yichen FanCasey Eye Institute at Oregon Health and Science University, 515 SW Campus Dr., Portland, OR, 97239, USA.
Zachary A KroegerCasey Eye Institute at Oregon Health and Science University, 515 SW Campus Dr., Portland, OR, 97239, USA.
Christina J FlaxelCasey Eye Institute at Oregon Health and Science University, 515 SW Campus Dr., Portland, OR, 97239, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Acute idiopathic maculopathy (AIM) is a posterior segment disorder that involves the neurosensory retina, retinal pigment epithelium, and choroidal circulation. When first described, the disease was classified as unilateral, but subsequent reports have found bilateral presentations. There is growing evidence to suggest the coxsackie virus as the etiology, however, other pro-inflammatory conditions have also been temporally linked to fundoscopic findings. We report on a young male without viral prodrome and without known contact with viral illnesses who experienced bilateral recurrent acute idiopathic maculopathy. Observations: A 35-year-old male presented with retinal whitening within the macula of the right eye. Multimodal imaging demonstrated a bacillary layer detachment, late leakage, and disruption of the choriocapillaris. Laboratory workup for inflammatory and infectious etiologies was negative. A diagnosis of AIM was made. The findings resolved with a steroid course. Nine months after initial presentation, the patient developed similar symptoms, fundoscopic, and imaging findings in the left eye, which again resolved with a steroid course. Three years after initial presentation, he developed symptoms in the right eye. Fundoscopy and imaging demonstrated a larger affected area compared to the prior episode. At his last follow up, the visual acuity, fundoscopy, and imaging findings had returned to baseline with no residual acuity deficit. Conclusions and importance: The patient presented has recurrent, bilateral AIM. Bilateral presentations and recurrent presentations have previously been reported, but this case is unique as it meets both criteria. Based on multimodal imaging throughout each episode, we hypothesize that AIM may be on the white dot disease spectrum.

Indexed as

Acute idiopathic maculopathyAPMPPERelentless placoidSpectrumWhite dot syndrome

Identifiers

PMID39469422
PMCPMC11513792

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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.