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Updated: Feb 1, 2026

Porcine Model of Infrarenal Abdominal Aortic Aneurysm
Published on: November 21, 2019
A super-elderly case of abdominal aortic aneurysm associated with chronic disseminated intravascular coagulation
Kazunori Otsui1, Mai Yamamoto2, Humiaki Aoki2
1Department of Cardiovascular Medicine, Kobe Rosai Hospital, Kobe, Japan.
Insights
A large abdominal aortic aneurysm (AAA) caused chronic disseminated intravascular coagulation (DIC) in an elderly woman. Anti-fibrinolytic therapy with tranexamic acid successfully treated her coagulopathy, highlighting the importance of monitoring AAA and coagulation.
Area of Science:
- Vascular Surgery
- Hematology
- Internal Medicine
Background:
- Chronic disseminated intravascular coagulation (DIC) is a known complication of aortic aneurysms.
- Abdominal aortic aneurysms (AAA) can lead to complex hemostatic abnormalities.
Observation:
- An elderly Japanese woman presented with massive purpura, diagnosed with DIC.
- She had a progressively enlarging abdominal aortic aneurysm (AAA) with significant mural thrombosis.
- The AAA was identified as the sole cause of her coagulopathy.
Findings:
- The patient's thrombocytopenia and purpura correlated with the exacerbation of her AAA.
- Anti-fibrinolytic therapy using tranexamic acid effectively improved the DIC and coagulopathy.
- Intraluminal thrombosis within the AAA was a key factor in the observed coagulopathy.
Implications:
- This case underscores the need to evaluate AAA diameter and intraluminal thrombosis in patients with coagulopathy.
- Regular monitoring of coagulation and fibrinolysis is crucial for managing patients with AAA.
- Anti-fibrinolytic therapy can be a successful treatment for DIC associated with AAA.
Abstract:
Chronic disseminated intravascular coagulation (DIC) is a well-known complication of aortic aneurysm. A 91-year-old Japanese woman was admitted to our hospital because of massive purpura of the lower limbs. The presence of abdominal aortic aneurysm (AAA) had been pointed out from the age of 80 years, and its diameter had gradually increased. The AAA was composed of two portions, that is, a large upper and a small lower portion, and a large mural thrombosis was observed in the lower portion. The laboratory data led to the diagnosis of DIC, and AAA was the only identifiable cause of coagulopathy. The time course of exacerbation of AAA was consistent with the progression of thrombocytopenia and purpura. Therefore, we concluded that AAA was the underlying cause of DIC. Since DIC in aortic aneurysms is associated with excessive fibrinolysis, tranexamic acid was administered as anti-fibrinolytic therapy. After that, coagulopathy was drastically improved. Our patient responded successfully to anti-fibrinolytic therapy for coagulopathy. The present case illustrates the importance of evaluation of the diameter of an aneurysm as well as intraluminal thrombosis, which may play an important role in coagulopathy including DIC. It is necessary to monitor coagulation and fibrinolysis for the follow-up of patients with AAA. <Learning objective: We present a case report of an aged Japanese woman with abdominal aortic aneurysm associated with disseminated intravascular coagulation, and anti-fibrinolytic therapy drastically ameliorated her condition. Our case illustrates the importance of evaluation of the diameter of an aneurysm as well as conducting follow-up monitoring of coagulation and fibrinolysis.>.
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