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巨细胞性心肌炎的心血管磁共振成像与心内膜心肌活检:关于诊断挑战及未来展望的病例报告

Cardiovascular magnetic resonance imaging and endomyocardial biopsy in giant cell myocarditis: a case report on diagnostic challenges and future perspectives.

作者信息

Gronwald Judith, Klingel Karin, Schuster Andreas, Lange Torben

机构信息

Department of Cardiology and Pneumology, University Medical Center of Göttingen, Georg-August University Göttingen and German Centre for Cardiovascular Research (DZHK), Partner Site Lower Saxony, Robert-Koch-Str. 40, 37075 Göttingen, Germany.

Cardiopathology, Institute for Pathology and Neuropathology, University Hospital Tübingen, Liebermeisterstr. 8, 72076 Tübingen, Germany.

出版信息

Eur Heart J Case Rep. 2025 Jun 4;9(6):ytaf276. doi: 10.1093/ehjcr/ytaf276. eCollection 2025 Jun.

Abstract

BACKGROUND

Giant cell myocarditis (GCM) is a rare but often fast-progressing cardiac disease with a high risk of poor outcome. Nonetheless, its differentiation from other diseases like cardiac sarcoidosis (CS) using cardiovascular magnetic resonance imaging (CMR) remains challenging.

CASE SUMMARY

A 27-year-old male patient presented to the emergency department with acute cardiac decompensation and severely reduced left ventricular ejection fraction. After exclusion of an ischaemic cause of heart failure, CMR was performed, showing signs of acute inflammation and late gadolinium enhancement patterns that were indistinguishable between GCM and CS. Despite the suspicion of sarcoidosis based on a lymph node biopsy, endomyocardial biopsy (EMB) provided clear evidence of typical histopathological changes consistent with GCM. An immunosuppressive therapy was initiated leading to an improvement in left ventricular function.

DISCUSSION

Cardiovascular magnetic resonance imaging is an important cornerstone in the diagnostic pathway of GCM, however, only complementary use with EMB allows reliable diagnosis. Therefore, full diagnostic and especially prognostic potential of CMR remains unclear but offers an important starting point for optimizing patient management.

摘要

背景

巨细胞性心肌炎(GCM)是一种罕见但进展通常较快的心脏疾病,预后不良风险高。尽管如此,利用心血管磁共振成像(CMR)将其与其他疾病如心脏结节病(CS)区分开来仍具有挑战性。

病例摘要

一名27岁男性患者因急性心脏失代偿和左心室射血分数严重降低就诊于急诊科。排除心力衰竭的缺血性病因后,进行了CMR检查,显示出急性炎症迹象和钆延迟强化模式,在GCM和CS之间无法区分。尽管基于淋巴结活检怀疑为结节病,但心内膜心肌活检(EMB)提供了与GCM一致的典型组织病理学变化的明确证据。开始免疫抑制治疗后,左心室功能得到改善。

讨论

心血管磁共振成像在GCM的诊断途径中是一个重要基石,然而,只有与EMB互补使用才能实现可靠诊断。因此,CMR的全部诊断潜力,尤其是预后潜力仍不明确,但为优化患者管理提供了一个重要的起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/726c/12204184/93ce47a121c8/ytaf276il2.jpg

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