Evidence map›Paper›PMID 42595918›Full record

ArticleVirchows Archiv : an international journal of pathology2026

Extensive myocardial disarray in hearts with normal cardiac mass: a concealed cardiomyopathic phenotype with histological overlap with hypertrophic cardiomyopathy.

Yukiko Hata, Yoshiaki Yamaguchi, Keiichi Hirono, Shojiro Ichimata, Naoki Nishida

Abstract read
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Article in Virchows Archiv : an international journal of pathology, 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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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Yukiko HataDepartment of Legal Medicine, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
Yoshiaki YamaguchiDepartment of Cardiology, Saiseikai Takaoka Hospital, Toyama, Japan.
Keiichi HironoDepartment of Pediatrics, Faculty of Medicine, University of Toyama, Toyama, Japan.
Shojiro IchimataDepartment of Legal Medicine, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan.
Naoki NishidaDepartment of Legal Medicine, Faculty of Medicine, University of Toyama, 2630 Sugitani, Toyama, 930-0194, Japan. nishida@med.u-toyama.ac.jp.ORCID http://orcid.org/0000-0002-6921-1768

Funding

Japan Society for the Promotion of Science London JP23H03759Japan Society for the Promotion of Science London JP25K02899
6 · The paper itself

Abstract

Extensive myocardial disarray is a characteristic histopathological feature of hypertrophic cardiomyopathy (HCM), but its occurrence in hearts with normal cardiac mass remains poorly characterized. We reviewed 2,823 consecutive forensic autopsies and identified 1,387 hearts with normal cardiac weight. Ten cases (0.72%) demonstrated extensive type Ia myocardial disarray involving contiguous myocardial regions. Histopathological findings, clinical information, and genetic data were analyzed, and matched controls (n = 20) were selected for comparison. Disarray was accompanied by moderate-to-severe fibrosis and small intramural arterial abnormalities. Three individuals fulfilled criteria for sudden cardiac death, and none had been diagnosed with HCM during life. Matched controls lacked comparable disarray and demonstrated significantly less fibrosis. Genetic analysis identified rare variants in cardiomyopathy-associated genes, although most were classified as variants of uncertain significance. Extensive myocardial disarray and fibrosis can occur in hearts with normal cardiac mass. Although these findings do not establish a diagnosis of HCM, they define a concealed cardiomyopathic phenotype with histological overlap with HCM. Recognition of such abnormalities may improve pathological evaluation of sudden death cases currently classified as structurally normal at autopsy.

Indexed as

AutopsyGenetic analysisHypertrophic cardiomyopathyMyocardial disarraySudden death

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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.