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Multiple thromboembolism with multiple causes in a 69-year-old woman: a case report
Luigi Iuliano1, Maria Misuraca, Alessandro Varroni
1Department of Medical Sciences and Biotechnology, Vascular Medicine and Atherothrombosis Laboratory, Sapienza University of Rome, corso della Repubblica 79, IT-04100 Latina, Italy. luigi.iuliano@uniroma1.it.
Insights
Recurrent arterial embolisms in a 69-year-old woman were linked to multiple causes, including JAK2 mutation and aortic mural thrombosis. A comprehensive diagnostic approach identified several thrombosis sources, leading to effective treatment.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Diagnostic Imaging
Background:
- Recurrent arterial embolisms necessitate precise etiological diagnosis.
- A 69-year-old woman experienced multiple arterial embolisms, initially attributed to atrial fibrillation.
Purpose of the Study:
- To investigate the complex etiology of recurrent arterial embolisms in a patient with multiple thrombosis sources.
- To highlight the importance of a comprehensive diagnostic strategy beyond conventional approaches.
Main Methods:
- Systematic utilization of advanced imaging procedures.
- Re-evaluation of blood tests to identify underlying causes of thrombosis.
- Clinical case presentation of a 69-year-old Italian Caucasian woman.
Main Results:
- Identification of thrombocytosis associated with the JAK2 V617F mutation.
- Detection of rare mural thrombosis in the descending aorta and pulmonary artery.
- Possible diagnosis of a clinically silent patent ductus arteriosus as an initiating event.
Conclusions:
- A multi-faceted diagnostic approach revealed multiple embolisms from diverse sites and causes.
- This comprehensive analysis surpassed the conventional single-cause diagnostic strategy.
- Effective treatment involved warfarin, aspirin, hydroxyurea, and surgical intervention.
Introduction:
Aggressive, recurrent embolisms require accurate etiologic diagnosis. We describe the case of a 69-year-old Italian Caucasian woman with recurrent arterial embolisms in whom several sources and triggers of thrombosis were detected.
Case Presentation:
The patient, a 69-year-old Italian Caucasian woman, presented with a systemic embolism that was initially attributed to atrial fibrillation. The recurrence of embolisms despite anti-thrombotic therapy prompted a re-evaluation of the clinical presentation. New potential causes of thrombosis emerged in this patient, including thrombocytosis associated with the JAK2 V617F mutation and the very rare mural thrombosis of the descending aorta. A mural thrombus in the pulmonary artery was detected contiguous with the aortic mural thrombosis, raising the possibility of a clinically silent ductus Botalli as the initiating event. The patient was treated with warfarin, aspirin, hydroxyurea, and surgery.
Conclusions:
The diagnosis was achieved via systematic use of imaging procedures and reconsideration of blood tests performed to explore the diagnosis of thrombosis. This allowed a deeper and more detailed analysis of the case beyond the conventional approach, which would have aimed to identify one cause for the condition at hand, in this case, atrial fibrillation. The broader approach that we used resulted in the diagnosis of multiple embolisms from multiple sites and multiple causes.
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