# Scarce Duet in One Heartbeat: A Case Report on Yamaguchi and Myocardial Bridging

**Authors:** Nada Saleh, Lama El Mawla, Zeinab Shaito, Ahmad H Alhajj Mohammad, Majd Khalil

PMC · DOI: 10.7759/cureus.104531 · Cureus · 2026-03-02

## TL;DR

This case report describes a rare combination of Yamaguchi syndrome and myocardial bridging in a patient with a history of cardiac arrest.

## Contribution

The paper highlights the rare coexistence of Yamaguchi syndrome and myocardial bridging, emphasizing diagnostic challenges and management.

## Key findings

- The patient exhibited apical hypertrophy with non-obstructive LVOT physiology.
- The combination of Yamaguchi syndrome and myocardial bridging may increase arrhythmogenic and ischemic risks.
- The case underscores the importance of recognizing this rare condition to avoid misdiagnosis as acute coronary syndrome.

## Abstract

Among the various types of hypertrophic cardiomyopathies (HCM) is an apical hypertrophic cardiomyopathy (ApHCM) variant, also known as Yamaguchi syndrome. It is a rare condition mostly found in Japanese patients and is characterized by the special Ace-of-Spades morphology of the left ventricular cavity. The coexistence of ApHCM and myocardial bridging is an uncommon finding. This rare association may create a complex arrhythmogenic and ischemic substrate, potentially increasing the risk of adverse cardiac events.

In our patient, echocardiography demonstrated an apical wall thickness of 17 mm, a left ventricular outflow tract (LVOT) maximum peak gradient of 3.45 mmHg, and a LVOT mean gradient of 2.47 mmHg, along with a global longitudinal strain (GLS) value of −15.8%, consistent with a non-obstructive LVOT physiology.

While its symptoms coincide with those of acute coronary syndrome (ACS), clinicians should maintain a high index of suspicion for this disease, as it is often unrecognized. This paper documents the rare coexistence of Yamaguchi syndrome and myocardial bridging in a patient with a previous history of cardiac arrest, highlighting its rarity, discussing the diagnostic challenges due to symptoms mimicking acute coronary syndrome (ACS), and emphasizing the importance of careful management and follow-up in affected patients.

## Linked entities

- **Diseases:** acute coronary syndrome (MONDO:0005542)

## Full-text entities

- **Diseases:** ACS (MESH:D054058), ischemic (MESH:D002545), Yamaguchi syndrome (MESH:C537096), HCM (MESH:D002312), ApHCM (MESH:D000092183), cardiac arrest (MESH:D006323), Myocardial Bridging (MESH:D054084)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13041092/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13041092/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC13041092/full.md

---
Source: https://tomesphere.com/paper/PMC13041092