Incidental finding of sclerosing angiomatoid nodular transformation of the spleen

Wien Klin Wochenschr. 2012 Feb;124(3-4):100-3. doi: 10.1007/s00508-011-0101-1. Epub 2011 Dec 5.

Abstract

Background: The prevalence of tumors in the spleen is rare; most tumors are benign and of vascular origin. In 2004 a vascular lesion was first described, the sclerosing angiomatoid nodular transformation (SANT), which is a benign lesion with good circumscription and multinodular angiomatoid appearance. We report a case of this rare tumor in the spleen which was incidentally found in a patient with a tumorous lesion in the pancreatic tail.

Case report: A 69-year-old patient was referred to our hospital with a tumor in the pancreatic tail which was suspicious for cancer. Radiologic work-up revealed furthermore a 4 cm in diameter large lesion central in the spleen suspicious for metastasis of the pancreatic tumor. The patient underwent surgery and a distal pancreatectomy with splenectomy was performed. Histologic specimen obtained a sclerosing angiomatoid nodular transformation in the spleen. The operative and postoperative course was uneventful.

Conclusions: SANT of the spleen are very rare tumors and should be considered as an important differential diagnosis to other vascular lesions.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Diagnosis, Differential
  • Histiocytoma, Benign Fibrous / pathology*
  • Histiocytoma, Benign Fibrous / surgery*
  • Humans
  • Incidental Findings
  • Male
  • Neoplasms, Multiple Primary / pathology*
  • Neoplasms, Multiple Primary / surgery*
  • Pancreatic Neoplasms / pathology
  • Pancreatic Neoplasms / surgery
  • Splenectomy
  • Splenic Neoplasms / pathology*
  • Splenic Neoplasms / surgery*
  • Treatment Outcome