Key result
A 69-year-old man with heart failure and atrial fibrillation developed bilateral atrial appendage thrombosis and disseminated intravascular coagulation due to Morganella morganii infection, resulting in fatal cardiogenic shock.
Why the study?
Simultaneous left and right atrial appendage thrombosis is rare in AF, and its association with DIC from the emerging pathogen Morganella morganii had not yet been described.
Case Report (n=1)
This case highlights the rare occurrence of bilateral atrial appendage thrombosis as a complication of disseminated intravascular coagulation in the context of Morganella morganii infection.
Background The simultaneous occurrence of left atrial appendage (LAA) and right atrial appendage (RAA) thrombosis is a rare finding in atrial fibrillation (AF). In addition, concomitant conditions, such as heart failure (HF) and disseminated intravascular coagulation (DIC), could be associated with intracardiac thrombosis. Morganella morganii is an emerging pathogen, and the association with DIC and cardiac thrombosis is not yet described. Case summary A 69-year-old Caucasian man was admitted to the hospital for progressive dyspnoea and new-onset diarrhoea. His physical examination revealed signs of HF and new-onset AF; laboratory tests showed marked thrombocytopaenia and coagulopathy. Blood and urine cultures were positive for M. morganii, and the International Society on Thrombosis and Hemostasis criteria were diagnostic for DIC. Transthoracic echocardiogram revealed a large, mobile left atrial mass and severely reduced left ventricular function. Transoesophageal echocardiogram showed two masses: one in the LAA and one in the RAA. Positron emission tomography/computed tomography scan excluded infective endocarditis and malignancies. After the beginning of antibiotic therapy and anticoagulation, the patient developed severe bleeding. Unfortunately, his haemodynamic status was complicated by multi-organ failure, and at the end, he developed irreversible cardiogenic shock. We present this challenging case of HF and AF complicated by DIC in the context of M. morganii infection. Discussion Multiple mechanisms, such as inflammatory storm, activation of coagulation cascade, and amplified immune response, may explain the hyper-coagulable state related to DIC. In our case, HF, AF, and DIC may have facilitated RAA thrombosis, which is a rare finding. To the best of our knowledge, this is the first reported case of concomitant cardiac thrombosis as a complication of DIC in the context of M. morganii infection. This highlights the need among clinicians for an increased awareness about this pathogen and the complications of its infection.
No takes yet. Share an insight, caveat, or question.
Mazzeo et al. (2025) conducted a case report in Heart failure, atrial fibrillation, disseminated intravascular coagulation, Morganella morganii infection (n=1). Morganella morganii infection was evaluated on Clinical course (multi-organ failure and cardiogenic shock). A 69-year-old man with heart failure and atrial fibrillation developed bilateral atrial appendage thrombosis and disseminated intravascular coagulation due to Morganella morganii infection, resulting in fatal cardiogenic shock.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: