A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE最新文献_第2页

A Tale of Broken Hearts: Cardiac Aspergillosis in an Immunocompromised Patient 心碎的故事:免疫功能低下患者的心脏曲霉病

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1801

T. Malik, B. Gordon, R. Ramanathan, E.L. Mcguire

引用次数: 0

Cardiac Arrest From Superior Mesenteric Artery Syndrome 肠系膜上动脉综合征引起的心脏骤停

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1803

G. Guzmán, P.N.F. Tawfik

引用次数: 0

Alerted by the Wrong Electrogram: A Case of Cardiac Arrest Post Succinylcholine Administration During an Electroencephalogram 错误的心电图提示:1例脑电图中给药琥珀胆碱后心脏骤停

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1811

P. Adderley, C. Tejera Quesada, C. Dorta

引用次数: 0

Trust But Verify: Torsades With a Normal QTc 信任但要验证:具有正常QTc的扭转

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1799

K. Roman, R. Centor, A. Heudebert

引用次数: 0

Aortic Dissection: Rare Complication of Fibromuscular Dysplasia 主动脉夹层:纤维肌肉发育不良的罕见并发症

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1809

M. Malik, I. Kovalenko, K. Golubykh, H. Qurashi, Q. Uddin

引用次数: 0

A Unique Case Presentation of Takotsubo Cardiomyopathy After Cardiac Arrest and Resuscitation Without CPR 心脏骤停后无心肺复苏术复苏的Takotsubo心肌病一例

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1787

M. Gwiazdowski, S. Niraula, B. Bewley

引用次数: 0

How Big Is Too Big? A Case of Ruptured Abdominal Aortic Aneurysm 多大才算太大?腹主动脉瘤破裂1例

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1810

K. Golubykh, I. Kovalenko, N. Pourhabibi Zarandi, N. Ramesh

引用次数: 0

Lone Atrial Septal Aneurysm: "Steaming Teapot" - Is Long-term Anticoagulation and Surveillance Warranted? 单独房间隔动脉瘤:“蒸汽茶壶”-长期抗凝和监测是必要的吗?

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1798

K. Rajak, A. Halder, A. Atrash

引用次数: 0

A Case of Uncontrolled Atrial Flutter in a Patient With Known Mac Requiring Prophylactic Intubation and Mechanical Ventilation for Rate Control 已知Mac患者不受控制的心房扑动需要预防性插管和机械通气来控制心率1例

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1802

S. Avera, I. Ogbuka, S. Harris, S. El-Chemeitelli

引用次数: 0

Calcified Amorphous Tumor of the Heart 心脏钙化无定形肿瘤

A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE Pub Date : 2023-05-01 DOI: 10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1788

H. Alrahamneh, A. E. Orellana

{"title":"Calcified Amorphous Tumor of the Heart","authors":"H. Alrahamneh, A. E. Orellana","doi":"10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1788","DOIUrl":"https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a1788","url":null,"abstract":"Alport syndrome is a heterogeneous genetic disease caused by mutation in the genes that codify the type IV collagen of the basement membrane, which produces an overexpression of proteins in the extracellular matrices of the basement membrane, leading to glomerulosclerosis, which principally affects the kidneys, eyes, and inner ear. We present the case of a 35-year-old male with hypertension and chronic kidney failure caused by Alport syndrome, on haemodialysis since having rejected kidney transplants on 2 occasions, and fitted with a permanent central venous catheter as other vascular access was not possible. He was admitted with a profile of septic shock with suspected endocarditis or an infection site at the central catheter. Transaesophageal and transthoracic echocardiograms were taken, in which there were no signs of endocarditis, but which showed a mass of 33×23 mm along the right atrial wall and the Eustachian valve at the height of the inferior vena cava; the mass was nearly immobile, pedicled, and not calcified, and did not figure on the echocardiogram as a cardiac thrombus (Figure 1). Heparin, intravenous antibiotherapy and fluids were administered; with this treatment, the patient was stable and without fever in 48 hours. In the 20 days that followed, he underwent echocardiograph tests without any observable changes in the mass. For this reason, we opted for a surgical intervention and extracted a fragment approximately 25 mm in diameter with an excrescent area of 20×15×14 mm with a whitish colour, from the wall of the right atrium at the union of the inferior vena cava. Under the microscope, we observed an amorphous eosinophilic material with extensive calcifications, with fibrous tissue containing small vessels from hypertrophic walls and stromal micro-haemorrhage in the base (Figure 2). The anatomopathologic diagnosis was of an intraatrial tumor consistent with calcified amorphous tumor (CAT). The postoperative period was without complications. A postoperative echocardiograph test was performed, which detected no remains of the extirpated tumourous mass. Two months later, the patient remained asymptomatic. CAT, described for the first time in 1997, is an infrequent cause of non-neoplastic intracardiac mass. Histologically, it is characterised by nodular calcium deposits over a matrix of fibrin and/or amorphous fibrinlike material, hyalinisation, inflammatory cells, and degenerated haematologic elements. It has been linked to organised thrombi, but its precise aetiology is unknown. Clinical tests usually show them to be benign, although they may cause obstruction or embolism, and cases can evolve fatally. The presence of cardiac CAT in haemodialysis patients has been described. During differential diagnosis, cardiac neoplasias, especially myxomas, and fibromas are considered, particularly if they are calcified, and so are conditions involving infection or thrombosis; in our case, there was no histologic data involving any of these pos","PeriodicalId":112405,"journal":{"name":"A50. CRITICAL CARE CASE REPORTS: CARDIAC AND VASCULAR DISEASE","volume":"10 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128045315","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