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Splenic Sclerosing Angiomatoid Nodular Transformation in an 8-Year-Old Child

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 d...

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Bibliographic Details
Published in:Journal of the Korean Society of Radiology 2025, 86(1), , pp.191-198
Main Authors: Kim, Ji Yeong, Lee, Hee Jung, Jung, Eun Young, Lee, Hye Won, Shim, Ye Jee
Format: Article
Language:English
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Summary: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.
ISSN:2951-0805
2951-0805
DOI:10.3348/jksr.2024.0017