Splenic Sclerosing Angiomatoid Nodular Transformation in an 8-Year-Old Child
- Author:
Ji Yeong KIM
1
;
Hee Jung LEE
;
Eun Young JUNG
;
Hye Won LEE
;
Ye Jee SHIM
Author Information
- Publication Type:Case Report
- From: Journal of the Korean Society of Radiology 2025;86(1):191-198
- CountryRepublic of Korea
- Language:English
- 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.
