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Dynamic right ventricular outflow tract obstruction due to straight back syndrome and funnel chest – A pediatric case 直背综合征和漏斗胸导致的右心室流出道动态阻塞--一个儿科病例
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.008

Thoracic deformity affects circulatory dynamics, and postural changes may affect hemodynamics. We report on the case of a 10-year-old girl with straight back syndrome (SBS) and funnel chest in which a right ventricular outflow tract (RVOT) obstruction was demonstrated by dynamic echocardiography. The patient occasionally experienced chest discomfort in the standing and sitting positions. Chest radiography and computed tomography showed SBS and funnel chest as well as limited anteroposterior chest space. Although she had a grade 3 systolic ejection murmur due to RVOT obstruction, it disappeared in the supine position. The cardiothoracic ratio was 56 % in the supine position but increased to 67 % in the upright position. Echocardiography showed that the RVOT was maintained in the supine (1.0 m/s) but narrowed in the sitting (1.7 m/s) position. This is the first pediatric case showing RVOT obstruction during the upright position that has been shown by dynamic echocardiography. Dynamic echocardiography in both positions may be useful for evaluating RVOT stenosis.

Learning objective

Patients with straight back syndrome and funnel chest have limited anteroposterior chest space, which may cause posture-dependent right ventricular outflow tract (RVOT) obstruction. Dynamic echocardiography in the supine and sitting position is useful to detect posture-dependent RVOT obstruction, which can be also observed in the pediatric population.

胸廓畸形会影响循环动力学,而体位变化可能会影响血液动力学。我们报告了一例患有直背综合征(SBS)和漏斗胸的 10 岁女孩的病例,动态超声心动图显示其右室流出道(RVOT)阻塞。患者在站立和坐位时偶尔感到胸部不适。胸部放射线检查和计算机断层扫描显示出 SBS 和漏斗胸以及胸腔前后间隙受限。虽然由于 RVOT 阻塞,她出现了 3 级收缩期射血杂音,但在仰卧位时杂音消失了。仰卧位时的心胸比例为 56%,但直立位时增加到 67%。超声心动图显示,仰卧位(1.0 米/秒)时 RVOT 保持不变,但坐位(1.7 米/秒)时 RVOT 变窄。这是第一例通过动态超声心动图显示直立位时 RVOT 阻塞的儿科病例。学习目标直背综合征和漏斗胸患者的胸前空间有限,这可能会导致姿势依赖性右室流出道(RVOT)阻塞。仰卧位和坐位动态超声心动图有助于检测姿势依赖性 RVOT 梗阻,这种梗阻也可在儿科人群中观察到。
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引用次数: 0
A case of “late adult type” of ALCAPA syndrome in a 76-year-old woman 一名 76 岁女性的 "晚成人型 "ALCAPA 综合征病例
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.006

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare condition; late adult presentation is extremely rare but, with modern diagnostics, more asymptomatic or mildly symptomatic elderly patients with ALCAPA are found. A 76-year-old woman was admitted to our emergency department in December 2021 with fever, fatigue, cognitive-motor slowing, and hyposthenia of left hemisoma. Cranium computed tomography (CT) was performed, with no signs of stroke. Contrast-enhanced CT, performed with electrocardiogram-gated technique, showed a dilatated left coronary artery arising directly from the main pulmonary artery; right coronary artery was markedly dilated and tortuous and characterized by multiple inter-coronary collateral arteries with left coronary artery, in particular in the retro-aortic side and along the cone artery. ALCAPA syndrome represents one of the most common causes of myocardial ischemia in children and, if left untreated, results in a mortality rate of up to 80–90 % within the first year of life. In our case, no previous history of cardiological disease was found that could have suggested this type of condition. This is extremely rare, especially if we consider that our patient reached the 8th decade of life.

Learning objectives

  • ALCAPA syndrome can present in adulthood.

  • Collaterals between coronary arteries are essential to guarantee the survival into adulthood.

  • Cardiac computed tomography imaging is essential for the diagnosis.

左冠状动脉肺动脉起源异常(ALCAPA)是一种罕见病;成人晚期发病极为罕见,但随着现代诊断技术的发展,发现了更多无症状或症状轻微的老年 ALCAPA 患者。2021 年 12 月,一名 76 岁的妇女因发热、乏力、认知-运动迟缓和左侧血肿亢进被送入我院急诊科。进行了头颅计算机断层扫描(CT),未发现中风迹象。使用心电图门控技术进行的对比增强 CT 显示,左冠状动脉扩张,直接来自主肺动脉;右冠状动脉明显扩张和迂曲,与左冠状动脉之间有多条冠状动脉侧支,尤其是在主动脉后侧和沿锥动脉处。ALCAPA 综合征是导致儿童心肌缺血的最常见原因之一,如果不及时治疗,第一年内的死亡率高达 80-90%。在我们的病例中,没有发现任何心脏病病史,因此无法推断出这种类型的病症。学习目标:ALCAPA 综合征可在成年后出现。
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引用次数: 0
A case of severely progressive left atrial calcification triggered by inflammation due to radiofrequency catheter ablation 一例因射频导管消融引发炎症而导致左心房严重进行性钙化的病例
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.009

Left atrial calcification (LAC) has been reported in 13.8 % of patients after atrial fibrillation (AF) ablation, which is related with stiff LA physiology and increased cardiovascular events. We describe a case in which long-term persistence of atrial inflammation caused by radiofrequency catheter ablation (RFCA) resulted in LAC. A 73-year-old man who underwent three previous AF ablations presented to our institution with a chief complaint of shortness of breath upon exertion. Electrocardiography showed a normal sinus rhythm, and transthoracic echocardiography revealed mild pulmonary hypertension. A marked decrease was observed in the mitral Doppler A-wave. Right heart catheterization showed marked V-wave augmentation in the pulmonary artery wedge pressure waveform despite the absence of mitral regurgitation, leading to a diagnosis of stiff LA syndrome. Computed tomography images revealed atrial wall thickening consistent with the ablation sites 6 months after the first ablation, which reflected inflammation-induced edema. LAC occurred at the site of atrial wall edema and expanded over several years. Mitral Doppler tracing showed a decrease in the A-wave two years and nine months after the first detection of LAC. This case demonstrates inflammation-induced atrial edema can persist for months after RFCA and may adversely affect atrial function years later.

Learning objective

This case demonstrates inflammation-induced atrial edema can persist for months after radiofrequency catheter ablation and may adversely affect atrial function years later. Considering that left atrial calcification (LAC) was detected two years and nine months before atrial function declined in this case, early detection of LAC may be a predictor of future atrial function deterioration. Careful follow-up is recommended for patients with LAC.

据报道,13.8%的心房颤动(房颤)消融术后患者会出现左心房钙化(LAC),这与左心房生理学僵化和心血管事件增加有关。我们描述了一例因射频导管消融术(RFCA)导致心房炎症长期存在而导致 LAC 的病例。一名 73 岁的男子曾接受过三次房颤消融术,因主诉劳累后气短而到我院就诊。心电图显示窦性心律正常,经胸超声心动图显示轻度肺动脉高压。二尖瓣多普勒 A 波明显减弱。右心导管检查显示,尽管没有二尖瓣反流,但肺动脉楔压波形有明显的 V 波增强,因此诊断为僵硬 LA 综合征。第一次消融术后 6 个月,计算机断层扫描图像显示心房壁增厚,与消融部位一致,这反映了炎症引起的水肿。LAC 发生在心房壁水肿部位,并在数年内扩大。二尖瓣多普勒描记显示,在首次发现 LAC 的两年零九个月后,A 波有所减弱。本病例表明炎症引起的心房水肿可在射频导管消融术后持续数月,并可能在数年后对心房功能产生不利影响。考虑到本病例中左心房钙化(LAC)是在心房功能下降前两年零九个月发现的,因此早期发现 LAC 可能是预测未来心房功能恶化的一个指标。建议对左心房钙化患者进行仔细随访。
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引用次数: 0
Transcatheter edge-to-edge mitral valve repair for severe heart failure in a young woman with polymyositis: A case report 经导管二尖瓣边缘对边缘修补术治疗患有多发性肌炎的年轻女性的严重心力衰竭:病例报告
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.06.001
Masayoshi Fujii MD, Tetsuari Onishi MD, PhD, Hiroyuki Yamamoto MD, PhD, Nobuyuki Takahashi MD, Tomofumi Takaya MD, PhD, Hiroya Kawai MD, PhD, FJCC

Polymyositis (PM) and dermatomyositis (DM) are chronic inflammatory muscle disorders characterized by muscle weakness and fatigue. They are histopathologically defined by inflammatory cell infiltrates in the skeletal muscle. In a recent meta-analysis, the incidence of cardiovascular complications in patients with PM/DM ranged from 9 to 72 %, with heart failure being the most commonly reported heart disease. In cases of heart failure accompanied by severe mitral regurgitation that is refractory due to guideline-directed medical therapy, the transcatheter edge-to-edge mitral valve repair (TEER) procedure using the MitraClip (Abbott Vascular, Santa Clara, CA, USA) offers an alternative therapeutic approach. We present a pioneering case report describing the successful application of TEER in a young woman with drug-refractory heart failure due to cardiovascular involvement in PM.

Learning objective

  • In polymyositis (PM)/ dermatomyositis (DM), the most commonly reported clinical heart disorder is heart failure, with some cases attributed to mitral regurgitation.

  • Patients suffering from systemic inflammatory diseases such as PM/DM often face high surgical risk, and the MitraClip is an effective treatment modality.

多发性肌炎(PM)和皮肌炎(DM)是以肌肉无力和疲劳为特征的慢性肌肉炎症性疾病。它们的组织病理学特征是骨骼肌中的炎性细胞浸润。在最近的一项荟萃分析中,PM/DM 患者心血管并发症的发病率从 9% 到 72% 不等,其中心力衰竭是最常见的心脏病。对于伴有严重二尖瓣反流的心力衰竭病例,如果药物治疗无效,使用 MitraClip(雅培血管公司,美国加利福尼亚州圣克拉拉市)进行的经导管二尖瓣边缘到边缘修补术(TEER)提供了另一种治疗方法。学习目的-在多发性肌炎(PM)/皮肌炎(DM)中,最常见的临床心脏疾病是心力衰竭,其中一些病例归因于二尖瓣反流。
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引用次数: 0
Reply: Exploring the link between COVID-19 and coronary spasm 回复:探索 COVID-19 与冠状动脉痉挛之间的联系
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.003
Shingo Kato MD, PhD , Mai Azuma MD
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引用次数: 0
Estimating an embolic source in peripheral artery disease using non-obstructive general angioscopy and histopathology 利用非阻塞性普通血管造影和组织病理学估算外周动脉疾病的栓塞源
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.002

Spontaneously ruptured aortic plaques are known to scatter frequently. Peripheral artery disease (PAD) is assumed to be exacerbated by aortic embolism besides local atherosclerosis. However, it has been challenging to show where the embolic plug came from. We estimated the embolic source of PAD in a 78-year-old male with a history of repetitive occlusion in the right peroneal artery by demonstrating and sampling using non-obstructive angioscopy (NOGA) for peripheral arteries and the aorta. Screening of the aorta, the iliac artery, and the femoral artery by computed tomography angiography, and NOGA revealed aortic dissection in the infrarenal abdominal artery. Four puff-chandelier ruptures that scattered like puffs were detected, and sampling was successful from puff-chandelier ruptures in the thoracic aorta, in the suprarenal abdominal artery, and in the dissected infrarenal abdominal artery. Among three puff-chandelier ruptures, a puff-chandelier rupture in the dissected infrarenal abdominal artery had the highest homology regarding the structure and the degree of fatty globules and cholesterol crystals. Endovascular graft replacement in the infrarenal dissected abdominal artery stopped the patient's repeated worsening of PAD.

Learning objective

The potential cause of peripheral artery disease is embolism from the upstream arteries beside local atherosclerosis. Homological comparison between materials from the occluded site and scattering plaques at the aorta and upstream arteries may suggest the embolic mechanism. In this case, repetitive occlusion in the right peritoneal artery was attributed to the embolism from the dissected infrarenal aorta because the highest homology was shown between the dissected infrarenal aorta where stent graft replacement stopped worsening of peripheral artery disease.

众所周知,自发性破裂的主动脉斑块会经常分散。除局部动脉粥样硬化外,主动脉栓塞也会加重外周动脉疾病(PAD)。然而,要证明栓塞来自何处一直是个难题。我们通过使用非阻塞性血管造影术(NOGA)对外周动脉和主动脉进行演示和取样,估计了一名 78 岁男性 PAD 的栓塞源,该患者有右腓动脉反复闭塞的病史。通过计算机断层扫描血管造影术和非阻塞性血管造影术对主动脉、髂动脉和股动脉进行筛查后发现,腹主动脉夹层位于肾下动脉。在胸主动脉、肾上腹部动脉和剥离的肾下腹部动脉的 "噗噗-吊灯 "破裂处,发现了四处像 "噗噗 "一样散开的 "噗噗-吊灯 "破裂。在三处 "吊灯 "破裂中,解剖的腹主动脉下动脉的 "吊灯 "破裂在结构和脂肪球及胆固醇结晶的程度上具有最高的同源性。学习目的外周动脉疾病的潜在原因除了局部动脉粥样硬化外,还有来自上游动脉的栓子。将闭塞部位的材料与主动脉和上游动脉的散落斑块进行同源性比较,可提示栓塞机制。在本病例中,右腹膜动脉的重复性闭塞被认为是来自剥离的肾下主动脉的栓塞,因为在肾下主动脉的剥离处,支架移植的置换阻止了外周动脉疾病的恶化,两者之间的同源性最高。
{"title":"Estimating an embolic source in peripheral artery disease using non-obstructive general angioscopy and histopathology","authors":"","doi":"10.1016/j.jccase.2024.05.002","DOIUrl":"10.1016/j.jccase.2024.05.002","url":null,"abstract":"<div><p><span><span>Spontaneously ruptured aortic plaques are known to scatter frequently. </span>Peripheral artery disease (PAD) is assumed to be exacerbated by aortic embolism besides local </span>atherosclerosis<span><span><span>. However, it has been challenging to show where the embolic plug came from. We estimated the embolic source of PAD in a 78-year-old male with a history of repetitive occlusion in the right peroneal artery by demonstrating and sampling using non-obstructive angioscopy (NOGA) for </span>peripheral arteries<span> and the aorta. Screening of the aorta, the iliac artery, and the </span></span>femoral artery<span><span> by computed tomography angiography, and NOGA revealed </span>aortic dissection<span> in the infrarenal abdominal artery. Four puff-chandelier ruptures that scattered like puffs were detected, and sampling was successful from puff-chandelier ruptures in the thoracic aorta, in the suprarenal abdominal artery, and in the dissected infrarenal abdominal artery. Among three puff-chandelier ruptures, a puff-chandelier rupture in the dissected infrarenal abdominal artery had the highest homology regarding the structure and the degree of fatty globules and cholesterol crystals. Endovascular graft replacement in the infrarenal dissected abdominal artery stopped the patient's repeated worsening of PAD.</span></span></span></p></div><div><h3>Learning objective</h3><p>The potential cause of peripheral artery disease is embolism from the upstream arteries beside local atherosclerosis. Homological comparison between materials from the occluded site and scattering plaques at the aorta and upstream arteries may suggest the embolic mechanism. In this case, repetitive occlusion in the right peritoneal artery was attributed to the embolism from the dissected infrarenal aorta because the highest homology was shown between the dissected infrarenal aorta where stent graft replacement stopped worsening of peripheral artery disease.</p></div>","PeriodicalId":52092,"journal":{"name":"Journal of Cardiology Cases","volume":"30 3","pages":"Pages 63-66"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141281299","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Two-stage hybrid strategy for multivessel coronary artery disease and functional ischemic mitral regurgitation: A case series 治疗多支血管冠状动脉疾病和功能性缺血性二尖瓣返流的两阶段杂交策略:病例系列
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.004
Motoki Fukutomi MD, PhD , Kenji Wada MD , Tomoya Uchimuro MD , Mizuho Hoshina MD , Takayuki Onishi MD , Shuichiro Takanashi MD, PhD, FJCC , Tetsuya Tobaru MD, PhD, FJCC

The optimal treatment strategy of high surgical risk patients with multivessel coronary artery disease (CAD) and functional mitral regurgitation (MR) remains controversial. We present two cases in which two-stage hybrid treatment with prior transcatheter mitral valve edge-to-edge repair (TEER) followed by off-pump coronary artery bypass grafting (OPCAB) was successfully performed in patients with CAD and functional ischemic MR. In both cases, the patient showed good hemodynamic stability during OPCAB without an increase in MR. A two-stage hybrid strategy with prior TEER followed by OPCAB may be an ideal treatment option for high surgical risk patients with multivessel CAD and functional ischemic MR.

Learning objective

To recognize the effectiveness of a two-stage hybrid approach with transcatheter edge-to-edge repair and off-pump coronary artery bypass grafting in high surgical risk patients with multivessel coronary artery disease and functional mitral regurgitation.

多支血管冠状动脉疾病(CAD)和功能性二尖瓣反流(MR)高手术风险患者的最佳治疗策略仍存在争议。我们介绍了两例成功实施两阶段混合治疗的病例,即先进行经导管二尖瓣边缘到边缘修补术(TEER),然后再进行体外冠状动脉旁路移植术(OPCAB),用于治疗患有冠状动脉疾病和功能性缺血性二尖瓣反流的患者。在这两个病例中,患者在 OPCAB 期间均表现出良好的血流动力学稳定性,而 MR 并未增加。学习目的认识经导管边缘到边缘修复术和体外循环冠状动脉旁路移植术两阶段混合方法在多支血管冠状动脉疾病和功能性二尖瓣反流的高手术风险患者中的有效性。
{"title":"Two-stage hybrid strategy for multivessel coronary artery disease and functional ischemic mitral regurgitation: A case series","authors":"Motoki Fukutomi MD, PhD ,&nbsp;Kenji Wada MD ,&nbsp;Tomoya Uchimuro MD ,&nbsp;Mizuho Hoshina MD ,&nbsp;Takayuki Onishi MD ,&nbsp;Shuichiro Takanashi MD, PhD, FJCC ,&nbsp;Tetsuya Tobaru MD, PhD, FJCC","doi":"10.1016/j.jccase.2024.05.004","DOIUrl":"10.1016/j.jccase.2024.05.004","url":null,"abstract":"<div><p><span>The optimal treatment strategy of high surgical risk patients with multivessel coronary artery disease (CAD) and functional </span>mitral regurgitation<span><span> (MR) remains controversial. We present two cases in which two-stage hybrid treatment with prior transcatheter mitral valve<span> edge-to-edge repair (TEER) followed by off-pump coronary artery bypass grafting (OPCAB) was successfully performed in patients with CAD and functional ischemic MR. In both cases, the patient showed good </span></span>hemodynamic stability during OPCAB without an increase in MR. A two-stage hybrid strategy with prior TEER followed by OPCAB may be an ideal treatment option for high surgical risk patients with multivessel CAD and functional ischemic MR.</span></p></div><div><h3>Learning objective</h3><p>To recognize the effectiveness of a two-stage hybrid approach with transcatheter edge-to-edge repair and off-pump coronary artery bypass grafting in high surgical risk patients with multivessel coronary artery disease and functional mitral regurgitation.</p></div>","PeriodicalId":52092,"journal":{"name":"Journal of Cardiology Cases","volume":"30 3","pages":"Pages 67-70"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142117692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Percutaneous coronary intervention for iatrogenic coronary artery pseudoaneurysm at left main trunk bifurcation: A case report 经皮冠状动脉介入治疗左主干分叉处的先天性冠状动脉假性动脉瘤:病例报告
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.007

A 70-year-old man was referred to our hospital with a diagnosis of progressive increase in extravasation leading to an iatrogenic coronary artery (CA) pseudoaneurysm within a month of percutaneous coronary intervention (PCI). The pseudoaneurysm was located on the carina side of the proximal left descending artery (LAD) accompanied by peri-stent contrast staining around the left main trunk (LMT). After a shared decision-making process, a second PCI was performed to prevent CA pseudoaneurysm rupture owing to concerns of adhesion around the LMT and difficulty in approaching the carina side of the proximal LAD for surgery. Coil embolization with four coils was performed and kissing stents with two covered stents were implanted. After the “Double-D molding technique,” intravascular ultrasound imaging revealed only small residual spaces out of the stents. Final coronary angiography (CAG) revealed no contrast staining of the pseudoaneurysm. Four months after the PCI, follow-up CAG revealed no further pseudoaneurysm enlargement. To the best of our knowledge, this is the first case of PCI for a CA pseudoaneurysm at the LMT bifurcation treated using kissing stents with two covered stents.

Learning objective

Coil embolization and implantation of kissing stents with two covered stents with the “Double-D molding technique” is an optional method to stop further enlargement of the pseudoaneurysm at the left main trunk bifurcation.

一名 70 岁的男性在经皮冠状动脉介入治疗(PCI)后一个月内因外渗逐渐增加导致先天性冠状动脉(CA)假性动脉瘤而转诊至我院。假性动脉瘤位于左降支动脉(LAD)近心端,左主干(LMT)周围伴有支架周围造影剂染色。由于担心 LMT 周围粘连以及难以靠近 LAD 近端心尖一侧进行手术,经过共同决策,患者接受了第二次 PCI,以防止 CA 假性动脉瘤破裂。手术中使用了四个线圈进行栓塞,并植入了带有两个覆盖支架的吻合支架。采用 "双D成型技术 "后,血管内超声成像显示支架外仅有很小的残留空间。最终的冠状动脉造影(CAG)显示假性动脉瘤没有造影剂染色。PCI 术后四个月,随访的 CAG 显示假性动脉瘤没有进一步扩大。据我们所知,这是首例使用带两个覆盖支架的吻合支架对左主干分叉处的 CA 假性动脉瘤进行 PCI 治疗的病例。学习目标使用 "双 D 型技术 "进行线圈栓塞并植入带两个覆盖支架的吻合支架,是阻止左主干分叉处假性动脉瘤进一步扩大的一种可选方法。
{"title":"Percutaneous coronary intervention for iatrogenic coronary artery pseudoaneurysm at left main trunk bifurcation: A case report","authors":"","doi":"10.1016/j.jccase.2024.05.007","DOIUrl":"10.1016/j.jccase.2024.05.007","url":null,"abstract":"<div><p><span>A 70-year-old man was referred to our hospital with a diagnosis of progressive increase in extravasation leading to an iatrogenic coronary artery<span><span> (CA) pseudoaneurysm within a month of percutaneous coronary intervention (PCI). The pseudoaneurysm was located on the carina side of the proximal left descending artery (LAD) accompanied by peri-stent contrast staining around the left main trunk (LMT). After a shared decision-making process, a second PCI was performed to prevent CA pseudoaneurysm rupture owing to concerns of adhesion around the LMT and difficulty in approaching the carina side of the proximal LAD for surgery. </span>Coil embolization<span> with four coils was performed and kissing stents with two covered stents were implanted. After the “Double-D molding technique,” intravascular ultrasound imaging revealed only small residual spaces out of the stents. Final </span></span></span>coronary angiography (CAG) revealed no contrast staining of the pseudoaneurysm. Four months after the PCI, follow-up CAG revealed no further pseudoaneurysm enlargement. To the best of our knowledge, this is the first case of PCI for a CA pseudoaneurysm at the LMT bifurcation treated using kissing stents with two covered stents.</p></div><div><h3>Learning objective</h3><p>Coil embolization and implantation of kissing stents with two covered stents with the “Double-D molding technique” is an optional method to stop further enlargement of the pseudoaneurysm at the left main trunk bifurcation.</p></div>","PeriodicalId":52092,"journal":{"name":"Journal of Cardiology Cases","volume":"30 3","pages":"Pages 71-74"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141409866","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fibrin-associated diffuse large B-cell lymphoma in the aortic valve and ascending aorta 主动脉瓣和升主动脉中的纤维蛋白相关弥漫大 B 细胞淋巴瘤
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.011

Primary cardiac lymphoma is an extremely rare disease, with the most common being diffuse large B-cell lymphoma (DLBCL). Fibrin-associated diffuse large B-cell lymphoma (FA-DLBCL) has been classified as a rare and unusual type of lymphoma and is included in the category of DLBCL associated with chronic inflammation (DLBCL-CI). In this study, we report a case of FA-DLBCL in the aortic valve and ascending aorta of a 51-year-old-woman.

Learning objective

In this rare case of FA-DLBCL in the aortic valve and ascending aorta, we highlight the features of FA-DLBCL and its differences from DLBCL-CI.

原发性心脏淋巴瘤是一种极为罕见的疾病,最常见的是弥漫大B细胞淋巴瘤(DLBCL)。纤维蛋白相关弥漫大 B 细胞淋巴瘤(FA-DLBCL)已被归类为一种罕见和不寻常的淋巴瘤类型,并被列入与慢性炎症相关的 DLBCL(DLBCL-CI)类别。在本研究中,我们报告了一例主动脉瓣和升主动脉中的 FA-DLBCL 病例,患者是一名 51 岁的女性。学习目的在这例主动脉瓣和升主动脉中的 FA-DLBCL 罕见病例中,我们强调了 FA-DLBCL 的特征及其与 DLBCL-CI 的区别。
{"title":"Fibrin-associated diffuse large B-cell lymphoma in the aortic valve and ascending aorta","authors":"","doi":"10.1016/j.jccase.2024.05.011","DOIUrl":"10.1016/j.jccase.2024.05.011","url":null,"abstract":"<div><p><span>Primary cardiac lymphoma is an extremely rare disease, with the most common being diffuse large B-cell lymphoma (DLBCL). Fibrin-associated diffuse large B-cell lymphoma (FA-DLBCL) has been classified as a rare and unusual type of lymphoma and is included in the category of DLBCL associated with chronic inflammation (DLBCL-CI). In this study, we report a case of FA-DLBCL in the </span>aortic valve<span> and ascending aorta of a 51-year-old-woman.</span></p></div><div><h3>Learning objective</h3><p>In this rare case of FA-DLBCL in the aortic valve and ascending aorta, we highlight the features of FA-DLBCL and its differences from DLBCL-CI.</p></div>","PeriodicalId":52092,"journal":{"name":"Journal of Cardiology Cases","volume":"30 3","pages":"Pages 94-96"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141391240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fusobacterium necrophorum endocarditis with intracranial abscesses: A case report and review of the literature 伴有颅内脓肿的坏死分枝杆菌性心内膜炎:病例报告和文献综述
Q4 Medicine Pub Date : 2024-09-01 DOI: 10.1016/j.jccase.2024.05.005
Emily Wong MD , Clark Robinson MD , Parth Upadhyaya DO , Alvin Chandra MD , Bonnie C. Prokesch MD , Minji Kang MD

Fusobacterium species are obligate anaerobic Gram-negative bacilli that are non-spore forming. The two most common species tied to human disease are F. nucleatum and F. necrophorum. They are commensal organisms in the oropharynx, gastrointestinal tract, and genital tract of humans, but can cause invasive infections especially in the head and neck such as periodontal disease and Lemierre's syndrome. F. necrophorum is an uncommon cause of infective endocarditis. We present a case of a previously healthy male who developed F. necrophorum endocarditis with multiple sites of pyogenic abscess formation.

Learning objective

Even among anaerobes, which account for less than 1 % of infective endocarditis (IE) cases, Fusobacterium necrophorum is rare. Specific laboratory conditions are necessary for growth, leading to delays in diagnosis. Severe disease is common given its virulence and predisposition for thrombophlebitis. While uncommon, it is crucial to maintain a degree of suspicion for Fusobacterium IE especially in individuals without prior cardiac disease whose infections were preceded by potential head and neck source.

镰刀菌属是厌氧革兰阴性杆菌,不形成孢子。与人类疾病相关的两个最常见的菌种是 F. nucleatum 和 F. necrophorum。它们是人类口咽、胃肠道和生殖道中的共生菌,但可引起侵入性感染,尤其是头颈部感染,如牙周病和勒米尔综合征。F.necrophorum是一种不常见的感染性心内膜炎病原体。学习目的即使在厌氧菌中(占感染性心内膜炎(IE)病例的不到 1%),坏死镰刀菌也是罕见的。其生长需要特定的实验室条件,导致诊断延误。由于其毒力强,易引发血栓性静脉炎,因此严重的疾病很常见。虽然不常见,但对分枝杆菌 IE 保持一定程度的怀疑至关重要,尤其是对既往无心脏疾病且感染前可能有头颈部感染源的患者。
{"title":"Fusobacterium necrophorum endocarditis with intracranial abscesses: A case report and review of the literature","authors":"Emily Wong MD ,&nbsp;Clark Robinson MD ,&nbsp;Parth Upadhyaya DO ,&nbsp;Alvin Chandra MD ,&nbsp;Bonnie C. Prokesch MD ,&nbsp;Minji Kang MD","doi":"10.1016/j.jccase.2024.05.005","DOIUrl":"10.1016/j.jccase.2024.05.005","url":null,"abstract":"<div><p><span><span>Fusobacterium</span></span> species are obligate anaerobic Gram-negative bacilli that are non-spore forming. The two most common species tied to human disease are <em>F. nucleatum</em> and <em>F. necrophorum.</em><span><span><span> They are commensal organisms in the oropharynx<span>, gastrointestinal tract, and genital tract of humans, but can cause invasive infections especially in the head and neck such as </span></span>periodontal disease and </span>Lemierre's syndrome. </span><em>F. necrophorum</em><span> is an uncommon cause of infective endocarditis. We present a case of a previously healthy male who developed </span><em>F. necrophorum</em><span> endocarditis with multiple sites of pyogenic abscess formation.</span></p></div><div><h3>Learning objective</h3><p><span>Even among anaerobes<span>, which account for less than 1 % of infective endocarditis (IE) cases, </span></span><span><span>Fusobacterium necrophorum</span></span><span> is rare. Specific laboratory conditions are necessary for growth, leading to delays in diagnosis. Severe disease is common given its virulence and predisposition for thrombophlebitis. While uncommon, it is crucial to maintain a degree of suspicion for </span><em>Fusobacterium</em><span> IE especially in individuals without prior cardiac disease whose infections were preceded by potential head and neck source.</span></p></div>","PeriodicalId":52092,"journal":{"name":"Journal of Cardiology Cases","volume":"30 3","pages":"Pages 75-78"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142117753","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Cardiology Cases
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