A case of sclerosing angiomatoid nodular transformation of the spleen
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Updated: May 7, 2026

Robot-assisted Partial Splenectomy
Published on: January 2, 2026
A Giorlandino1, R Caltabiano, S Lanzafame
1Department G.F. Ingrassia, Section of Anatomic Pathology, University of Catania, Italy.
Abstract:
Sclerosing angiomatoid nodular transformation of the spleen is a rare benign vascular lesion with extensive sclerosis and unknown aetiology. Although its pathogenesis is not clear, it has been postulated that it may represent a peculiar hamartomatous transformation of red pulp in response to an exaggerated non-neoplastic stromal proliferation. However, it is unclear whether SANT is the end stage of a variety of benign splenic conditions including inflammatory pseudotumour, hamartoma or hematoma. Considering that the lesion is benign, splenectomy is curative. We report a new case of SANT, discussing differential diagnosis, immunohistochemical profile and pathogenesis.
