Evidence map›Paper›PMID 41784417›Full record

ArticleTurk gogus kalp damar cerrahisi dergisi2026

Gorham-Stout disease presenting as chest wall defect: A case report and review of literature.

Athish Kannan Karur, Dinesh Kumar Sathanantham, Jayakumar Thanathu Krishnan Nair, Adinarayanan Kishore Nochur, Samuel Olaniyan

Abstract read
In one paragraph

Article in Turk gogus kalp damar cerrahisi dergisi, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Athish Kannan KarurClinic of General Medicine, Sri Devaraj Urs Medical College, Karnataka, Hindistan.ORCID 0009-0004-2154-1663
Dinesh Kumar SathananthamClinic of Cardiothoracic Vascular Surgery, Government Medical College Kottayam, Kerala, Hindistan.ORCID 0000-0002-7142-3348
Jayakumar Thanathu Krishnan NairClinic of Cardiothoracic Vascular Surgery, Government Medical College Kottayam, Kerala, Hindistan.ORCID 0000-0003-4106-269X
Adinarayanan Kishore NochurClinic of Cardiothoracic Vascular Surgery, Government Medical College Kottayam, Kerala, Hindistan.ORCID 0000-0003-3225-6564
Samuel OlaniyanClinic of Internal Medicine, Sri Sai PC, Indiana, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gorham-Stout disease (GSD), also known as vanishing bone syndrome, is an extremely rare, non-malignant condition marked by progressive osteolysis due to abnormal intraosseous lymphatic and vascular proliferation. Extensive chest wall involvement is particularly uncommon and can present without symptoms, complicating diagnosis and management. In this study, a review of similar cases in the literatures is tabulated with comparison of this case to other articles is presented. A 24-year-old male presented with an incidental finding of "hollowness" in his right chest wall following a muscle strain, but remained asymptomatic otherwise. Imaging revealed near-total disappearance of the right 4th to 6th ribs anterolaterally, and partial resorption of the 7

Indexed as

chest wall defectGorham-Stout diseasemassive osteolysisphantom bone diseasevanishing bone syndrome

Identifiers

PMID41784417
PMCPMC13051739

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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.