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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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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
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Lee, Hee Jung
Jung, Eun Young
Lee, Hye Won
Shim, Ye Jee
description 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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subjects computed tomography
magnetic resonance imaging
Pediatric Imaging
pediatrics
sclerosing angiomatoid nodular transformation
spleen
ultrasound
방사선과학
title Splenic Sclerosing Angiomatoid Nodular Transformation in an 8-Year-Old Child
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