Noori Muhammad Atif Masood, Shah Kalpesh, Fichadiya Hardik, Adeosun Mofe, Jesani Shrutie, Appiah-Kubi Edmund, Saeed Hasham, Elkattawy Sherif, Joshi Meherwan
Department of Medicine, Rutgers Health/Trinitas Regional Medical Center, Elizabeth, NJ, USA.
Department of Cardiology, St. Joseph's University Medical Center, Paterson, NJ, USA.
Eur J Case Rep Intern Med. 2022 Mar 1;9(3):003197. doi: 10.12890/2022_003197. eCollection 2022.
Aortic dissection is a relatively uncommon, although catastrophic, disease which requires early and accurate diagnosis and treatment for patient survival. Aortic dissection can be difficult to diagnose due to the diverse symptom presentation, which can lead to later diagnosis, resulting in a higher mortality rate. Here we present a case of type A aortic dissection with a varied symptom presentation, highlighting the importance of early detection and the Bentall procedure for management of such cases. A 50-year-old man with no known medical history presented with bilateral lower extremity swelling and fatigue for 2 weeks. The patient denied any chest pain or dyspnoea. Vital signs showed blood pressure of 160/76 mmHg, pulse of 103 bpm, respiratory rate of 18, and temperature of 36.7°C. Laboratory findings indicated a BNP of 1901 pg/ml and troponin of 0.5 ng/ml. An initial diagnosis of decompensated heart failure was made, and IV Lasix was started. Subsequently, an echocardiogram indicated an EF of 50-55% and ascending dissection of the aorta. A CT angiogram of the chest and abdomen confirmed this diagnosis. This patient presented with unusual symptoms of aortic dissection without the typical presentation of chest pain. It is important to consider aortic dissection in a cardiac-related case as prompt imaging can help confirm the diagnosis. We explore the risks and benefits of the Bentall procedure for the management and early detection of aortic dissection.
The absence of chest pain does not rule out aortic dissection as 50% of patients are pain free.It is critical to diagnose aortic dissection early in the disease course as mortality increases by 1% per hour from symptom onset.The aim of this study is also to raise awareness among healthcare professionals about the Bentall procedure in patients with type A aortic dissection involving the aortic valve.
主动脉夹层是一种相对罕见但极具灾难性的疾病,患者的生存需要早期准确的诊断和治疗。由于症状表现多样,主动脉夹层可能难以诊断,这可能导致诊断延迟,从而使死亡率升高。在此,我们报告一例症状表现多样的A型主动脉夹层病例,强调早期检测以及Bentall手术在此类病例管理中的重要性。一名50岁男性,无已知病史,出现双侧下肢肿胀和乏力2周。患者否认有任何胸痛或呼吸困难。生命体征显示血压为160/76 mmHg,脉搏为103次/分钟,呼吸频率为18次/分钟,体温为36.7°C。实验室检查结果显示脑钠肽(BNP)为1901 pg/ml,肌钙蛋白为0.5 ng/ml。初步诊断为失代偿性心力衰竭,并开始静脉注射速尿。随后,超声心动图显示射血分数(EF)为50 - 55%,升主动脉夹层。胸部和腹部CT血管造影证实了这一诊断。该患者出现了主动脉夹层的不寻常症状,而无典型的胸痛表现。在心脏相关病例中考虑主动脉夹层很重要,因为及时的影像学检查有助于确诊。我们探讨了Bentall手术在主动脉夹层管理和早期检测中的风险和益处。
胸痛的缺失并不排除主动脉夹层,因为50%的患者无疼痛症状。在疾病进程中早期诊断主动脉夹层至关重要,因为从症状发作起死亡率每小时增加1%。本研究的目的还在于提高医疗保健专业人员对涉及主动脉瓣的A型主动脉夹层患者进行Bentall手术的认识。