Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Case Report

Authors

  • Sayamaa Lkhagvadorj Department of Pathology, School of Biomedicine, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia
  • Sanchin Urjin Department of Surgery, Mongolia-Japan Teaching Hospital, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia
  • Usukhbayar Erdenebaatar Department of Surgery, Mongolia-Japan Teaching Hospital, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia
  • Batsaikhan Bat-Erdene Department of Surgery, School of Medicine, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia

DOI:

https://doi.org/10.24079/cajms.2019.09.009

Keywords:

Spleen, Hamartoma, CD34, Splenectomy

Abstract

Objectives: Sclerosing Angiomatoid Nodular Transformation (SANT) of the spleen is a rare benign vascular lesion with unknown etiology. Our purpose is to present our experience with this condition and review the available literature regarding it. Methods: This report depicts a pathologically proven case of SANT in a 32-year-old man with a history of two previous old injuries who presented with weight loss, vomiting and with left upper quadrant pain and an enlarged spleen. Results: The patient was successfully treated by splenectomy and diagnosed with SANT based on histological and immunohistochemical findings postoperatively. Conclusion: Most patients with SANT are asymptomatic. Imaging studies are essential for detection and the management of SANT. However, the final diagnosis can only be made by histopathology. SANT does not recur after splenectomy.

Abstract
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Published

2019-09-25

How to Cite

Lkhagvadorj, S., Urjin, S., Erdenebaatar, U., & Bat-Erdene, B. (2019). Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Case Report. Central Asian Journal of Medical Sciences, 5(3), 230–235. https://doi.org/10.24079/cajms.2019.09.009

Issue

Section

Case Reports