tricuspid valve

三尖瓣
  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    背景:右侧感染性心内膜炎,尤其是三尖瓣,是罕见且具有挑战性的诊断,通常表现为非特异性症状,并与高死亡率相关。此病例强调了管理此类疾病的复杂性以及早期诊断和多学科干预的重要性。
    方法:本案例研究详述了一名34岁女性的病史,该女性有静脉吸毒背景。她随后患上了真菌性三尖瓣心内膜炎,导致植被的形成延伸到上腔静脉。手术切除后的质量为15×3cm。
    结论:右侧感染性心内膜炎罕见,仅占5-10%的病例,三尖瓣心内膜炎更罕见。对内皮的损伤促进细菌附着,尤其是静脉吸毒者,金黄色葡萄球菌很常见。真菌性心内膜炎是罕见但致命的,死亡率高。诊断依赖于修改后的Duke标准,包括微生物和影像学证据.主要并发症影响瓣膜和全身区域。治疗p1rimarily涉及静脉抗生素,但持续性感染或严重并发症需要手术治疗.
    结论:该病例强调了早期诊断和干预在治疗右侧感染性心内膜炎中的重要性,尤其是真菌病理学和具有复杂病史的患者。
    BACKGROUND: Right-sided infective endocarditis, particularly of the tricuspid valve, is rare and challenging to diagnose, often presenting with nonspecific symptoms, and associated with high mortality rates. This case underscores the complexities in managing such conditions and the importance of early diagnosis and multidisciplinary intervention.
    METHODS: This case study details the medical history of a 34-year-old woman who had a background of intravenous drug abuse. She subsequently developed a fungal tricuspid valve endocarditis, leading to the formation of vegetation that extended into the superior vena cava. The mass measured 15 × 3 cm upon surgical removal.
    CONCLUSIONS: Right-sided infective endocarditis is rare, comprising only 5-10 % of cases, with tricuspid valve endocarditis being even rarer. Damage to the endothelium facilitates bacterial attachment, especially in IV drug users, with Staphylococcus aureus being common. Fungal endocarditis is rare but deadly, with high mortality. Diagnosis relies on the modified Duke criteria, including microbiological and imaging evidence. Major complications affect both valvular and systemic areas. Treatment p1rimarily involves IV antibiotics, but surgery is needed for persistent infections or severe complications.
    CONCLUSIONS: This case underscores the critical importance of early diagnosis and intervention in managing right-sided infective endocarditis, especially with a fungal pathology and in patients with complex medical histories.
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  • 文章类型: Case Reports
    我们报告了一例16岁的男性,患有由嗜肺Aggregatib杆菌引起的三尖瓣感染性心内膜炎并并发肺败血症栓塞。多种抗菌治疗不成功,需要手术治疗。在这份报告中,作者强调了高度怀疑心内膜炎及其可能的并发症的诊断的重要性.
    We report a case of a 16-year-old male with tricuspid valve infective endocarditis caused by Aggregatibacter aphrophilus and complicated by pulmonary septic embolisms. Multiple antimicrobial therapy was unsuccessful and surgical management was required. In this report, the authors highlight the importance of a high index of suspicion regarding the diagnosis of endocarditis and its possible complications.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
    背景:伯氏柯西氏菌是一种具有极端韧性和传染性的细菌,主要通过吸入污染的气溶胶传播。然而,正在讨论用蜱传递。我们报告了一例在城市环境中,远离绵羊繁殖的Q热引起的罕见右侧心内膜炎。
    方法:一名55岁男子,在该事件发生前健康状况良好,出现了三尖瓣氏杆菌心内膜炎。他没有与绵羊接触,也没有最近在农村甚至流行地区旅行。感染起源于严格的城市环境,以及病人在柏林的墓地园丁,再加上对野猪的短暂和局部接触,使这些动物的传播成为一个合理的假设。德国参考实验室证实了感染,在使用多西环素和氢氯喹治疗后,患者完全康复。
    结论:该病例报告的特点是右侧心内膜炎和在没有绵羊接触的大都市地区传播。我们认为,即使在非农村地区,这种情况也应有助于提高人们对Q热感染潜力的认识。
    BACKGROUND: Coxiella burnetii is a bacterium with extreme tenacity and contagiousness that is mainly transmitted by inhalation of contaminated aerosols. Nevertheless, a transmission by ticks is under discussion. We report a case of Q fever in an urban environment and far away from sheep breeding that caused a rare right-sided endocarditis.
    METHODS: A 55-year-old man who was in good health before the event developed a C. burnetii -endocarditis of the tricuspid valve. He had no contact with sheep and no recent travel in a rural or even endemic area. The infection originated in a strictly urban environment, and the patient\'s occupation as a cemetery gardener in Berlin, coupled with the close temporal and local exposure to wild boar, made a transmission by these animals a plausible hypothesis. The infection was confirmed by the German Reference Laboratory, and the patient recovered completely after treatment with doxycycline and hydrochlorquine.
    CONCLUSIONS: The specialities of this case report are the right-sided endocarditis and the transmission of C. burnetii in a metropolitan area without sheep contact. We think that this case should serve to increase awareness of the potential for Q fever infection even in non-rural areas.
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  • 文章类型: Case Reports
    据传闻,全身性房室瓣的经导管边缘到边缘修复(TEER)是一种可行的治疗选择,适用于先天性矫正大动脉转位的有症状的不能手术的成年患者(ccTGA)。然而,到目前为止,缺乏TEER治疗两个房室瓣的病例报告,特别是考虑到目前特定二尖瓣和三尖瓣TEER装置的可用性。
    我们介绍了一例84岁男性因两个房室瓣高度反流导致急性心力衰竭反复入院的病例。患者在这个高龄时首次被诊断为ccTGA,并接受了彻底的多模态成像方法,包括经胸和经食道超声心动图,心脏磁共振成像,心脏计算机断层扫描,和全身心室的心室造影。由于高的症状负担,尽管最佳的药物治疗和高剂量的利尿剂,心脏团队推荐TEER,首先是全身性三尖瓣,然后是非全身性二尖瓣。两种复杂的程序都很顺利,并导致生活质量的显着改善。
    先天性矫正的大动脉转位主要表现在成年期,并影响心室和房室瓣。如果对经胸超声心动图有解剖学怀疑,建议进行彻底的多模态成像检查.在这些通常无法手术的患者中,经导管治疗两个房室瓣似乎是安全有效的治疗选择。
    UNASSIGNED: Transcatheter edge-to-edge repair (TEER) for the systemic atrioventricular valve has been anecdotally reported as a viable treatment option in symptomatic inoperable adult patients born with congenitally corrected transposition of the great arteries (ccTGA). However, to date, case reports on TEER treatment of both atrioventricular valves are lacking, especially when considering the present availability of specific mitral and tricuspid valve TEER devices.
    UNASSIGNED: We present the case of an 84-year-old man with recurrent admissions for acute heart failure due to high-grade regurgitation of both atrioventricular valves. The patient was first diagnosed with ccTGA at this advanced age and underwent a thorough multimodality imaging approach, including transthoracic and transoesophageal echocardiography, cardiac magnetic resonance imaging, cardiac computed tomography, and ventriculography of the systemic ventricle. Due to the high symptom burden despite optimal medical therapy and high doses of diuretics, the heart team recommended TEER, first for the systemic tricuspid valve and later on for the non-systemic mitral valve. Both complex procedures were uneventful and led to considerable improvement in quality of life.
    UNASSIGNED: Congenitally corrected transposition of the great arteries mostly manifests itself in adulthood and affects both ventricles and atrioventricular valves. In case of anatomical doubts on transthoracic echocardiography, a thorough multimodality imaging work-up is recommended. Transcatheter treatment of both atrioventricular valves seems to be a safe and effective therapeutic option in these often inoperable patients.
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  • 文章类型: Case Reports
    感染性心内膜炎是一种罕见但危及生命的疾病,偶尔与不同的免疫学表现有关,包括混合型冷球蛋白血症.这可能导致冷球蛋白血症性血管炎,有可能导致广泛的器官损伤。尽管有些病例强调了感染性心内膜炎和冷球蛋白性血管炎之间的关系,没有针对这种组合进行全面的流行病学评估或最佳治疗策略.我们介绍了一例甲氧西林敏感的金黄色葡萄球菌感染性心内膜炎与冷球蛋白性血管炎相关的病例,并进行了文献综述,以比较类似病例的治疗和结局。我们的患者表现为经典的Meltzer三联征和轻度肾脏受累。冷冻免疫固定证实III型冷球蛋白血症,血清细胞因子显示IL-6水平升高。鉴别诊断包括感染性心内膜炎和慢性活动性丙型肝炎病毒感染。抗生素治疗后症状迅速缓解,确定感染性心内膜炎是冷球蛋白性血管炎的可能原因。我们的案例和文献综述强调,早期识别冷球蛋白性血管炎的病因对于选择适当的治疗方法和预防复发或发病率至关重要。
    Infective endocarditis is a rare but life-threatening condition, occasionally linked to diverse immunologic manifestations, including mixed cryoglobulinemia. This can lead to cryoglobulinemic vasculitis, which has the potential for widespread organ damage. Although some cases have highlighted the relationship between infective endocarditis and cryoglobulinemic vasculitis, no comprehensive epidemiological evaluation or optimal treatment strategies have been advanced for such a combination. We present a case of methicillin-sensitive Staphylococcus aureus infective endocarditis associated with cryoglobulinemic vasculitis and conduct a literature review to compare management and outcomes in similar cases. Our patient presented with classical Meltzer\'s triad and mild renal involvement. Cryoimmunofixation confirmed type III cryoglobulinemia, and serum cytokines showed elevated IL-6 levels. The differential diagnosis included infective endocarditis and chronic active hepatitis C virus infection. Rapid symptom resolution after antibiotic treatment identified infective endocarditis as the likely cause of cryoglobulinemic vasculitis. Our case and review of the literature highlight that early identification of the cause of cryoglobulinemic vasculitis is crucial for selecting appropriate treatment and preventing recurrence or morbidity.
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  • 文章类型: Case Reports
    除了经导管边缘到边缘修复(TEER),在评估中,二尖瓣和三尖瓣返流有新的介入治疗方案,例如通过假体完全替换瓣膜。
    一名78岁的既往冠状动脉搭桥术患者,有症状的严重二尖瓣返流和三尖瓣返流,通过经股动脉导管二尖瓣和三尖瓣假体依次治疗(Cardiovalve;CardiovalveLtd,以色列)由于二尖瓣解剖结构不利。首先进行经导管二尖瓣植入术(TMVI),并在三尖瓣返流进展后进行。1.5年后在三尖瓣位置(TTVI)植入第二个经导管瓣膜假体.成像显示二尖瓣和三尖瓣假体的双胎相似图像,并显示了经导管完全置换二尖瓣和三尖瓣的可能性。
    该病例显示了在单个患者中用于TMVI和TTVI的心脏瓣膜假体的可能性。特别是在TEER不合格的患者中,在设备批准后,这可能是一个很好的治疗选择。
    UNASSIGNED: Besides transcatheter edge-to-edge repair (TEER), there are new interventional treatment options for mitral and tricuspid regurgitation in evaluation, such as a complete replacement of the valve through a prosthesis.
    UNASSIGNED: A 78-year-old previous coronary artery bypass graft-operated patient with symptomatic severe mitral regurgitation and tricuspid regurgitation was sequentially treated by a transfemoral transcatheter mitral and tricuspid valve prosthesis (Cardiovalve; Cardiovalve Ltd, Israel) due to unfavourable mitral valve anatomy. The transcatheter mitral valve implantation (TMVI) was performed first and after progression of the tricuspid regurgitation, a second transcatheter valve prosthesis was implanted in tricuspid position (TTVI) 1.5 years later. Imaging showed a twin look-alike picture of a mitral and tricuspid prosthesis and showing the possibility of a complete transcatheter based replacement of the mitral and tricuspid valve.
    UNASSIGNED: This case shows the possibility of a Cardiovalve prosthesis being used for TMVI and TTVI in a single patient. Especially in TEER ineligible patients, it might be a good treatment option after device approval.
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  • 文章类型: Case Reports
    房室瓣降落伞畸形很少见,通常见于二尖瓣位置,叫做降落伞二尖瓣.到目前为止,很少在三尖瓣看到它,在文献回顾中,大约有14例三尖瓣降落伞异常。我们在这里介绍一名21岁的男性,他在几个月的时间里出现了进行性呼吸急促。尽管没有胸痛,心悸,或体重变化,检查显示一个柔软的,胸骨左下缘的全收缩期杂音。通过心电图和超声心动图的进一步检查发现了一种罕见的结构异常,称为降落伞三尖瓣,导致明显的三尖瓣反流,右房室轻度扩大。由于我国没有心胸外科医生,因此建议患者出国接受进一步治疗。
    Atrioventricular valve parachute deformity is rare and is generally seen in the mitral position, called the parachute mitral valve. It is rare to see it in the tricuspid valve and up to now, there have been approximately 14 cases of parachute abnormalities in tricuspid valves in a literature review. We present here a 21-year-old male who presented to the emergency department with progressive shortness of breath over several months. Despite the absence of chest pain, palpitations, or weight changes, examination revealed a soft, holosystolic murmur at the left lower sternal border. Further investigation through electrocardiogram and echocardiogram identified a rare structural abnormality known as parachute tricuspid valve, resulting in significant tricuspid regurgitation with mild right chamber enlargement. The patient was recommended to go abroad for further management since a cardiothoracic surgeon is not available in our country.
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  • 文章类型: Case Reports
    沙门氏菌骨关节受累是一种罕见的并发症,发生在约2%的病例中。化脓性关节炎极为罕见,仅涉及所有沙门氏菌病患者的0.2%。心内膜炎是另一种并发症,发生在不到0.8%的病例中。这些并发症更可能发生在免疫功能低下的患者中。
    我们报告了一位健康的25岁男性,他出现了左侧肢体疼痛。十天前,他的初级保健医生已经对他进行了布鲁氏菌病的治疗。关节穿刺术和随后的髋关节活检证实了沙门氏菌引起的化脓性关节炎。然而,他对治疗没有反应。我们没有发现潜在的免疫抑制。由于持续发烧和血培养阳性,进行了食管回声检查。它显示了幼稚三尖瓣的沙门氏菌心内膜炎。他通过关节切开术和抗生素治疗了四周。20个月后的随访显示没有潜在的免疫抑制。
    此病例突出表明,在沙门氏菌血培养阳性且感染病灶与沙门氏菌病相容但对治疗无反应的患者中,寻找其他感染灶是必要的。此外,布鲁氏菌病流行地区的医生应考虑发热和跛行患者的其他鉴别诊断,因为诊断沙门氏菌化脓性关节炎的任何延误都会破坏关节间隙,并造成终身不适.
    UNASSIGNED: Salmonella osteoarticular involvement is a rare complication, occurring in about 2% of the cases. Septic arthritis is exceedingly rare, involving only 0.2 % of all salmonellosis patients. Endocarditis is another complication that occurs in less than 0.8 % of cases. These complications are more likely to happen among immunocompromised patients.
    UNASSIGNED: We report a previously healthy 25-year-old man who presented with left limb pain. He had been treated for brucellosis ten days earlier by his primary care physician. Arthrocentesis and subsequent hip-joint biopsy confirmed septic arthritis due to Salmonella. However, he was unresponsive to the treatment. We found no underlying immunosuppression. A trans-esophageal echo was performed due to the continued fever and positive blood cultures. It revealed Salmonella endocarditis of the naïve tricuspid valve. He was treated via arthrotomy and antimicrobials for four weeks. Follow-up after 20 months showed no underlying immunosuppression.
    UNASSIGNED: This case highlights that in patients with positive Salmonella blood cultures and a focus of infection compatible with Salmonellosis but unresponsive to treatment, searching for other foci of infection is necessary. Furthermore, physicians in endemic areas of brucellosis should consider other differential diagnoses in patients with fever and limping because any delay in diagnosing Salmonella septic arthritis can destroy the joint space with lifelong discomfort.
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