J Korean Soc Radiol.
2025 Jan;86(1):191-198. 10.3348/jksr.2024.0017.
Splenic Sclerosing Angiomatoid Nodular Transformation in an 8-Year-Old Child
- Affiliations
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- 1Departments of Radiology, Keimyung University College of Medicine, Dongsan Hospital, Daegu, Korea
- 2Departments of Surgery, Keimyung University College of Medicine, Dongsan Hospital, Daegu, Korea
- 3Departments of Pathology, Keimyung University College of Medicine, Dongsan Hospital, Daegu, Korea
- 4Departments of Pediatrics, Keimyung University College of Medicine, Dongsan Hospital, Daegu, Korea
- KMID: 2564845
- DOI: http://doi.org/10.3348/jksr.2024.0017
Abstract
- Sclerosing angiomatoid nodular transformation (SANT) of the spleen is extremely rare in pediatric patients. Here, we report the case of an 8-year-old boy with iron-deficiency anemia and a solitary splenic mass detected using US, CT, and MRI. The patient underwent partial splenectomy, and the final diagnosis was SANT. Herein, we discuss the radiological features of splenic SANT through a review of reported cases and the differential diagnosis of other primary splenic tumors.
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