The Dilemma of Endomyocardial Biopsy Sampling for Lymphocytic Myocarditis Diagnosis [0.03%]
淋巴细胞性心肌炎诊断内膜心肌活检采样的困境
Tatsuya Shiraki,Rika Kawakami,Renu Virmani
Tatsuya Shiraki
Circ_0005372 targets the miR-153-3p/ITGB3 axis to stimulate the PI3K/AKT signaling pathway to facilitate the occurrence and development of congenital heart disease and pulmonary arterial hypertension in children [0.03%]
circ_0005372靶向miR-153-3p/ITGB3轴以刺激PI3K/AKT信号通路促进儿童先天性心脏病和肺动脉高压的发生发展
Mingyan Zhu,Guixiang Li,Yungui Li et al.
Mingyan Zhu et al.
Background: Congenital heart disease (CHD) is the most common and highest incidence of congenital malformations in newborn infants. Pulmonary arterial hypertension (PAH) is the most serious complication associated with CH...
Anatomical variations of the mitral leaflets: Unified and accessory scallops [0.03%]
二尖瓣瓣叶解剖变异：统一的和附加的瓣小叶
Buse Naz Çandir Gürses,Kader Yilar,Çağla Ergin et al.
Buse Naz Çandir Gürses et al.
Aim: To investigate the morphological variants of the leaflets and scallops of the mitral valve in fresh hearts of healthy individuals and to determine their morphometric values. ...
Fatal Rupture of a Giant Left Coronary Artery Aneurysm in an Infant with Kawasaki Disease. A Case Report with Systematic Literature Review [0.03%]
川崎病患儿巨大左冠状动脉瘤破裂致死1例并系统文献复习
Lai Jonathan K,López-Guillén José L,Yeung Rae S M et al.
Lai Jonathan K et al.
Kawasaki disease (KD) is a systemic vasculitis of childhood that may lead to coronary artery aneurysms. Rupture of a giant coronary aneurysm is an exceptionally rare but often fatal complication. We report the case of a 4-month-old infant w...
Revising the Histopathologic Definition of Myocarditis: Birth of the Seaport Criteria [0.03%]
心肌炎的病理定义修订：塞伯港标准的诞生
Gregory A Fishbein,Stephen D Preston
Gregory A Fishbein
Immuhistochemically-confirmed mitochondrial cardiomyopathy presenting as a conduction system hamartoma: A case report [0.03%]
免疫组化确认的线粒体心肌病表现为传导系统错构瘤的一例报告
Ryo Kaimori,Kentaro Sakai,Atsuhito Takeda et al.
Ryo Kaimori et al.
Conduction system hamartoma (CSH) is a rare cardiac lesion characterized by the abnormal proliferation of Purkinje-like myocytes. It predominantly affects female infants and is often associated with sudden cardiac death. Recent studies have...
The SCVP and AECVP 'Seaport Criteria' for Lymphocytic Myocarditis: retrospective application to an autopsy cohort [0.03%]
SCVP和AECVP淋巴细胞性心肌炎的“港口标准”：对尸检队列的回顾性分析
Sarah Parsons,Hans H de Boer
Sarah Parsons
Background: Diagnosing lymphocytic myocarditis in non-biopsy specimens remains challenging due to sampling variability, subjective interpretation of histology, and lack of standardized criteria. In 2025, the Society for C...
A case of cardiac undifferentiated pleomorphic sarcoma treated with post-operative radiotherapy followed by heart transplantation [0.03%]
术后放射治疗后进行心脏移植治疗心脏未分化多形性肉瘤一例报告
Sungyeon Jung,Eun Na Kim,Hye In Lee et al.
Sungyeon Jung et al.
Cardiac undifferentiated pleomorphic sarcomas (UPS) are extremely rare tumors that typically arise in the left atrium. They behave highly aggressively, requiring multimodality treatment when complete surgical resection is not feasible. Neve...
Lymphocytic myocarditis: A histopathologic definition and classification from the Society for Cardiovascular Pathology and Association for European Cardiovascular Pathology. I: Endomyocardial biopsy [0.03%]
淋巴细胞性心肌炎：来自心血管病理学会和欧洲心血管病理协会的组织病理学定义及分类（I）：心内膜心肌活检
Marc K Halushka,Giulia d&#x;Amati,Melanie C Bois et al.
Marc K Halushka et al.
Background and aim: Lymphocytic myocarditis has long been appreciated as a lymphocyte-predominant myocardial inflammation with resultant myocyte injury. However, current methods of diagnosis on endomyocardial biopsy (EMB)...
Cardiac Pathology in a Patient with a Novel Pathogenic Variant c.703del (p.Ile235SerfsTer4) of the TAFAZZIN Gene [0.03%]
TAFAZZIN基因新致病突变c.703del(p.Ile235SerfsTer4)患者的心脏病理学特征
Marisa Prasanpanich,Majid Husain,Nancy J Halnon et al.
Marisa Prasanpanich et al.
Introduction: Barth syndrome is a mitochondrial disease caused by loss-of-function mutations in the TAFAZZIN gene located on chromosome Xq28 encoding a transacylase essential for cardiolipin remodeling. Most patients deve...