Thiene Gaetano
Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padua, Via A. Gabelli, 86-35121 Padova, Italy.
Biology (Basel). 2025 Mar 18;14(3):306. doi: 10.3390/biology14030306.
A biopsy involves the removal of a piece or an entire organ from a living patient. The former began with open heart surgery (surgical pathology) and the latter with the recipient heart in cardiac transplantation. Transvenous or transarterial catheterization is the current procedure to performed endomyocardial biopsy with bioptome from the ventricles. This manoeuvre was first carried out by Werner Forssmann through a urological catheter in 1929, which he introduced into his radial left vein until it reached the RV. Then, in London in 1974, Richardson invented a new technique with a catheter via the right femoral vein, which he applied with success in patients with multiple myocardial diseases, both inflammatory and non-inflammatory. Subsequently, a transjugular endomyocardial biopsy was accomplished by Margaret Billingham to monitor heart rejection during cardiac transplantation. In the beginning, only histology for a light microscope, and rarely during electron microscopy, was employed. With the advent of molecular techniques and the discovery of polymerase chain reaction (PCR), molecular investigation became part of the gold standard for diagnosis involving EMB: histology, immunohistochemistry and molecular investigation, the latter in search of a viral cause. Nowadays, EMB is frequently employed in infiltrative (amyloidosis) and storage diseases (e.g., hemochromatosis and Fabry diseases). Diagnosis of myocarditis is now possible through Magnetic Cardiac Resonance (MCR), in place of BEM histology, thanks to oedema. With the help of ECMO, it is possible to allow the heart to rest, supporting its recovery from ejection fraction even in fulminant myocarditis. Cardiac transplantation with the pathological study of the recipient heart offers the opportunity to discover and study new diseases, like restrictive cardiomyopathy and a non-compacted left ventricle.
活检是指从活体患者身上切除一块组织或整个器官。前者始于心脏直视手术(外科病理学),后者始于心脏移植中的受体心脏。经静脉或经动脉导管插入术是目前使用活检钳从心室进行心内膜活检的方法。这一操作最早由维尔纳·福斯曼于1929年通过一根泌尿科导管进行,他将导管插入自己的左桡静脉,直至到达右心室。然后,1974年在伦敦,理查森发明了一种经右股静脉使用导管的新技术,并成功应用于患有多种心肌疾病(包括炎症性和非炎症性)的患者。随后,玛格丽特·比林厄姆完成了经颈静脉心内膜活检,以监测心脏移植过程中的排异反应。起初,仅采用光学显微镜组织学检查,很少进行电子显微镜检查。随着分子技术的出现和聚合酶链反应(PCR)的发现,分子研究成为心内膜活检诊断金标准的一部分:组织学、免疫组织化学和分子研究,后者用于寻找病毒病因。如今,心内膜活检常用于浸润性疾病(如淀粉样变性)和贮积病(如血色素沉着症和法布里病)。由于水肿,现在可以通过心脏磁共振成像(MCR)代替心内膜活检组织学检查来诊断心肌炎。借助体外膜肺氧合(ECMO),即使在暴发性心肌炎中,也有可能让心脏得到休息,支持其射血分数恢复。对受体心脏进行病理研究的心脏移植提供了发现和研究新疾病的机会,如限制性心肌病和左心室心肌致密化不全。