How to diagnose titanium hypersensitivity as a cause of arm swelling in a patient who underwent pacemaker implantation [0.03%]
如何诊断钛金属过敏作为心脏起搏器植入患者手臂肿胀的原因
Naoya Kataoka,Teruhiko Imamura
Naoya Kataoka
Needed on mapping findings and bipolar electrogram interpretation in double tachycardia [0.03%]
双室性心动过速的标测及双极电图判断要点
Naoya Kataoka,Teruhiko Imamura
Naoya Kataoka
Left atrial dominant cardiac sarcoidosis presenting with supraventricular tachycardia and left atrial myocardial damage: A case report [0.03%]
以阵发性室上性心动过速和左心房心肌损伤为表现的以左心房为主的心脏肉芽肿病一例报告
Ayaka Fujita,Takahiro Sakamoto,Shinichi Kurashima et al.
Ayaka Fujita et al.
A 61-year-old woman presented to our hospital with palpitations and dyspnea persisting for several months. Electrocardiography revealed atrial tachycardia, and X-ray revealed bilateral hilar enlargement. Computed tomography (CT) was perform...
A case of sinus of Valsalva-right ventricle fistula without an aneurysm complicated by aortic regurgitation [0.03%]
未伴动脉瘤的沃尔华氏窦至右心室瘘合并主动脉反流1例报告
Hiroki Okamoto,Hiroki Bansho,Kentaro Matsuoka et al.
Hiroki Okamoto et al.
A 70-year-old man with significant aortic regurgitation and a suspected ventricular septal defect presented with exertional dyspnea. Multimodality imaging showed a rare fistulous connection between the right ventricle and the sinus of Valsa...
Wild-type transthyretin amyloid cardiomyopathy diagnosed by 99mTc-HMDP scintigraphy and an endomyocardial biopsy despite inconclusive 99mTc-PYP findings [0.03%]
99mTc-PYP检查结果不明确的情况下，通过99mTc-HMDP显像和心内膜活检确诊野生型转甲状腺素蛋白淀粉样变性心肌病
Yusuke Kashiwagi,Satoshi Ito,Utaro Taga et al.
Yusuke Kashiwagi et al.
Transthyretin amyloid cardiomyopathy (ATTR-CM) is a progressive but under-diagnosed disease. With the emergence of novel therapies, including transthyretin (TTR) stabilizers and RNA silencers, an accurate diagnosis and timely therapeutic in...
Atrial leadless device dislodgment and intracardiac echocardiogram (ICE)-guided device retrieval after leadless pacemaker implantation: A case report [0.03%]
无导线起搏器植入后的器械移位及 ICE 指引下再捕获：一例报告
Kaiyu Jia,Shahkar Khan,Vincent Gallo et al.
Kaiyu Jia et al.
Background: Compared to traditional transvenous pacemakers, leadless pacemakers have the advantages of reducing risks of infection, minimal vascular access, and interactions with tricuspid apparatus. However, complication...
Unexpected presentation of post-implantation syndrome in a patient following aortoiliac aneurysm endovascular repair [0.03%]
腹主动脉瘤内修复术后髂动脉支架内狭窄致移植肾后腹膜脓肿伴急性排斥反应
Dung Duc Doan,Hoa Quynh Nguyen,Khuyen Kim Thi Hoang et al.
Dung Duc Doan et al.
Surgery and endovascular repair remain the standard treatments for those at high risk of aneurysm rupture. Early detection and timely intervention, such as surgery or endovascular aortic repair (EVAR), are critical. EVAR is preferred due to...
Emergency mitral valve transcatheter edge-to-edge repair in cardiogenic shock due to papillary muscle rupture [0.03%]
由于乳头肌破裂导致的心源性休克中的紧急经皮二尖瓣缘对缘修复术
Usman Ahmed,Christopher Kim,Camila Machado De Souza et al.
Usman Ahmed et al.
Cardiogenic shock secondary to papillary muscle rupture carries high mortality and often precludes surgical repair. We present a case of acute mitral regurgitation following myocardial infarction managed with emergent transcatheter edge-to-...
Biatrial tachycardia due to conduction recovery of left atrial anterior roof lesion created by vein of Marshall ethanol infusion [0.03%]
马歇尔静脉乙醇消融左心房前顶病变所致双向异位心动过速及其传导恢复机制的病例报告
Shushi Nishiwaki,Satoshi Shizuta,Hirohiko Kohjitani et al.
Shushi Nishiwaki et al.
A 77-year-old man underwent pulmonary vein isolation and cavotricuspid isthmus ablation for paroxysmal atrial fibrillation and typical atrial flutter. Eleven months later, recurrent atrial fibrillation required a second procedure. Left atri...
Cardiac magnetic resonance findings in two cases of hypertrophic cardiomyopathy with MYH7 and MYBPC3 variants: Limitations of genotype-based phenotypic prediction [0.03%]
MYH7和MYBPC3变异型肥厚心肌病的磁共振心血管影像表现：基于基因分型预测表型的局限性
Hidetaka Hayashi,Seitaro Oda,Masafumi Kidoh et al.
Hidetaka Hayashi et al.
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiomyopathy, usually caused by sarcomeric variants such as MYH7 and MYBPC3. However, genotype-phenotype correlations remain incompletely defined. We report two patients with ...