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Coeliac trunk dissection causing splenic infarction: a comprehensive review
Yousaf Zafar1, Laura Meidl1, Maddison Lonney1
1Internal Medicine, University of Missouri Kansas City, Kansas City, MO, USA.
Insights
A spontaneous coeliac trunk dissection caused splenic infarct in a 49-year-old man. This case highlights the importance of considering rare vascular events in abdominal pain diagnosis and management.
Area of Science:
- Vascular Surgery
- Gastroenterology
- Radiology
Background:
- Spontaneous coeliac trunk dissection is a rare vascular emergency.
- Splenic infarct can be a complication of coeliac trunk dissection.
- Abdominal pain is a common presenting symptom, but atypical presentations exist.
Observation:
- A 49-year-old man presented with acute epigastric pain radiating to the right shoulder after physical exertion.
- CT angiography revealed dissection of the coeliac trunk extending into the splenic artery, causing splenic infarct.
- Initial anticoagulation was complicated by retroperitoneal hemorrhage.
Findings:
- The patient was managed conservatively with aspirin for secondary prevention.
- Review of literature identified other cases of splenic infarct secondary to spontaneous coeliac trunk dissection.
- Outcomes varied depending on the extent of dissection and management strategies.
Implications:
- This case underscores the need for high clinical suspicion for visceral artery dissection in patients with unexplained abdominal pain.
- Early diagnosis via CT angiography is crucial for appropriate management.
- Conservative management with antiplatelet therapy may be a viable option in select cases of splenic infarct due to coeliac trunk dissection.
Abstract:
We describe the case of a 49-year-old man who presented with a 6-day history of epigastric abdominal pain radiating to his right shoulder which started suddenly after swinging a golf club. A CT angiography of the abdomen was performed which showed dissection of the coeliac trunk extending into the splenic artery and splenic infarct. Anticoagulation was initially started but discontinued due to a small retroperitoneal haemorrhage. The patient remained stable and was discharged on aspirin 325 mg for 1 month followed by aspirin 81 mg. We present this case as well as a review of previously reported cases of splenic infarct due to spontaneous coeliac trunk dissection with the treatments employed as well as the outcomes.
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