ArticleCureus2025
Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Case Report Highlighting Diagnostic Challenges and the Role of Immunohistochemistry.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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5 authors.
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Abstract
Sclerosing angiomatoid nodular transformation (SANT) of the spleen is a rare, benign vascular lesion that poses significant diagnostic challenges owing to its nonspecific clinical and radiological features. We herein report the case of a 35-year-old male who presented with chronic left hypochondrial pain and was found to have a splenic mass with poor enhancement on computed tomography (CT) and an increased fluorodeoxyglucose uptake on positron emission tomography-CT. Total splenectomy was performed, and a histopathological examination revealed well-demarcated angiomatoid nodules with varying vascular channels, fibrosclerosis, and hemosiderin deposition. Immunohistochemistry revealed a characteristic tri-phenotypic vascular profile of CD34
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