Kasula Varun, Padala Vikram, Doad Jagroop, Awais Hassan, Chaubey Vinod, Sood Aditya, Golden Lauren
Department of Cardiology, Campbell University School of Osteopathic Medicine, Lillington, North Carolina, USA.
Department of Cardiology, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, USA.
Case Rep Cardiol. 2025 May 9;2025:5514172. doi: 10.1155/cric/5514172. eCollection 2025.
Despite advances in imaging and diagnostics, calcific constrictive pericarditis (CCP) remains a rare and challenging entity, often masquerading as other cardiopulmonary conditions, leading to delayed diagnosis. We present a 70-year-old male with a history of heart failure, atrial fibrillation (AF), cirrhosis, chronic obstructive pulmonary disease (COPD), and prior pleural effusion, who was admitted with acute hypoxic respiratory failure and AF with rapid ventricular response (RVR). Imaging revealed extensive pericardial calcifications, leading to a diagnosis of CCP. The patient's clinical course was marked by refractory hypotension, altered mental status, and progressive cardiohepatic syndrome. Given his high surgical risk, he was managed conservatively and transitioned to palliative care. This case underscores the diagnostic and therapeutic challenges of CCP, particularly in patients with complex comorbidities where surgical intervention is not feasible. It highlights the need for early recognition and individualized management strategies to optimize outcomes in this challenging subset of patients.
尽管在影像学和诊断方面取得了进展,但钙化性缩窄性心包炎(CCP)仍然是一种罕见且具有挑战性的疾病,常常伪装成其他心肺疾病,导致诊断延迟。我们报告一名70岁男性,有心力衰竭、心房颤动(AF)、肝硬化、慢性阻塞性肺疾病(COPD)病史及既往胸腔积液史,因急性低氧性呼吸衰竭和伴有快速心室率(RVR)的AF入院。影像学检查显示广泛的心包钙化,从而诊断为CCP。患者的临床病程以难治性低血压、精神状态改变和进行性心肝综合征为特征。鉴于其手术风险高,对其进行了保守治疗并转入姑息治疗。该病例强调了CCP的诊断和治疗挑战,尤其是在合并复杂疾病而无法进行手术干预的患者中。它凸显了早期识别和个体化管理策略对于优化这一具有挑战性的患者亚组的治疗效果的必要性。