Evidence map›Paper›PMID 40718310›Full record

ArticleCureus2025

A Case in Which the Endoscopic Denker's Approach Was Useful in the Diagnosis of IgG4-Related Ophthalmic Disease.

Yusei Yamaguchi, Shinya Ohira, Ryousuke Yui, Satoshi Sonobe, Kota Wada

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Yusei YamaguchiOtolaryngology, Toho University, Tokyo, JPN.
Shinya OhiraOtolaryngology, Toho University, Tokyo, JPN.
Ryousuke YuiOtolaryngology, The Jikei University School of Medicine, Tokyo, JPN.
Satoshi SonobePathology, Toho University, Tokyo, JPN.
Kota WadaOtolaryngology, Toho University, Tokyo, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgG4-related disease (IgG4-RD) is a chronic inflammatory condition characterized by elevated serum IgG4 levels, infiltration of IgG4-positive plasma cells, and fibrosis in various organs. We report the case of a 76-year-old man who presented with left-sided proptosis. Computed tomography revealed a mass lesion in the left orbit. An initial biopsy via a transnasal approach under local anesthesia was inconclusive. Although endoscopic sinus surgery was performed under general anesthesia, a definitive diagnosis could not be obtained. The lesion continued to enlarge, and subsequent ophthalmologic examinations revealed progressive optic nerve compression. Therefore, tumor resection was performed again under general anesthesia using the endoscopic Denker's approach. The tumor was successfully resected without complications. Histopathological findings led to a diagnosis of probable IgG4-related ophthalmic disease (IgG4-ROD). Following surgery, the residual lesion enlarged again; however, a three-day course of steroid pulse therapy resulted in reduction of the lesion and improvement of optic nerve compression. The patient has remained relapse-free. While 81% of IgG4-ROD cases involve the lacrimal gland, other orbital structures such as the pterygopalatine fossa, trigeminal nerve branches, extraocular muscles, orbital fat, eyelids, and nasolacrimal duct can also be affected. In cases without lacrimal gland involvement, the optimal approach for obtaining diagnostic biopsy specimens should be considered individually. Although there is no consensus on the required volume of tissue for diagnosis, we believe that aggressive resection of the central lesion is necessary for accurate diagnosis. The endoscopic Denker's approach facilitates wide exposure and resection of far lateral maxillary sinus lesions, enabling both decompression and definitive diagnosis, which can lead to appropriate subsequent treatment.

Indexed as

endoscopic sinus surgeryoptic nerve compressionorbital tumorprobablesteroids

Identifiers

PMID40718310
PMCPMC12296910

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