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Updated: Jun 6, 2026

Laparoscopic Splenectomy with Pericardial Devascularization for Hypersplenism and Esophageal Variceal Hemorrhage Due to Portal Hypertension
Published on: November 15, 2024
Massive hemoperitoneum with splenic infarction in Evans syndrome
Eun Mi Ryu1, Soo Ah Im, Ho Jong Chun
1Department of Radiology, Seoul St. Mary's Hospital, The Catholic University of Korea, Republic of Korea.
Evans syndrome, a rare autoimmune disorder, can lead to severe complications. This case highlights splenic rupture and hemoperitoneum, a rare but critical event in pediatric patients.
Area of Science:
- Hematology
- Autoimmunology
- Pediatric Medicine
Background:
- Evans syndrome is a rare autoimmune hematologic disorder.
- It involves hemolytic anemia and immune thrombocytopenia.
- Complications typically include bleeding, rarely thrombosis.
Observation:
- An 18-month-old male with Evans syndrome presented with splenic infarction and rupture.
- This led to massive hemoperitoneum.
- Splenic artery embolization was performed.
Findings:
- This case demonstrates an extremely rare presentation of Evans syndrome.
- Splenic infarction and rupture are unusual complications.
- Successful splenic artery embolization was achieved.
Implications:
- Highlights the potential for severe vascular complications in Evans syndrome.
- Emphasizes the importance of prompt diagnosis and intervention.
- Informs management strategies for rare pediatric hematologic emergencies.
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