Clinical Identification and Characteristic Analysis of Giant Cell Myocarditis in 12 Cases

Shangyu Liu1, Lihui Zheng1, Lishui Shen1

  • 1State Key Laboratory of Cardiovascular Disease, National Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Insights

Giant cell myocarditis (GCM) is often misdiagnosed. Early diagnosis via endomyocardial biopsy improves outcomes for this rare, aggressive heart condition.

Area of Science:

  • Cardiology
  • Pathology

Background:

  • Giant cell myocarditis (GCM) is a rare and aggressive cardiomyopathy with high mortality.
  • Prompt diagnosis and treatment are crucial for managing GCM.

Purpose of the Study:

  • To analyze the clinical manifestations and progression of patients with Giant cell myocarditis.
  • To evaluate diagnostic delays and accuracy in GCM cases.

Main Methods:

  • Retrospective analysis of 12 patients diagnosed with GCM via endomyocardial biopsy (EMB) or during heart transplantation (HTx).
  • Collected data included demographics, cardiac function, arrhythmias, and preliminary diagnoses.
  • Compared diagnostic timelines and cardiac damage between EMB and HTx diagnosis groups.

Main Results:

  • GCM was frequently misdiagnosed initially as other cardiomyopathies or myocarditis.
  • Patients diagnosed via EMB had shorter symptom-onset-to-diagnosis times (6.6 months) and better left ventricular ejection fraction (47.2%) compared to HTx diagnoses (11.0 months, 31.4%).

Conclusions:

  • Pathological examination of myocardial tissue is essential for accurate GCM diagnosis.
  • Endomyocardial biopsy enables earlier identification of GCM, potentially improving patient outcomes.

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