Sclerosing angiomatoid nodular transformation of the spleen masquerading as a sarcoma metastasis

Lalitha M. Sitaraman, John G. Linn, Kristina A. Matkowskyj, Jeffrey D. Wayne

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

We report a case of sclerosing angiomatoid nodular transformation (SANT) of the spleen presenting as an incidental splenic mass in a patient with a history of retroperitoneal spindle cell sarcoma. Imaging studies and preoperative fine needle biopsy failed to differentiate this lesion from other vascular splenic lesions or a metastatic focus of a prior sarcoma. The patient was treated with splenectomy, which has proved both diagnostic and therapeutic in this and other cases of SANT. Although histology can lead to the diagnosis of vascular tumor, immuno - histochemistry is the only way to confirm the diagnosis of SANT. The etiology of SANT is unknown. SANT of the spleen is a benign lesion that does not recur after splenectomy.

Original languageEnglish (US)
Pages (from-to)124-125
Number of pages2
JournalRare Tumors
Volume2
Issue number4
DOIs
Publication statusPublished - Nov 19 2010

    Fingerprint

Keywords

  • Hamartoma
  • Hemangioendothelioma
  • Histology
  • Immunohistochemistry
  • Littoral cell angioma
  • Lymphangioma
  • Pathology
  • Sarcoma
  • Sclerosing angiomatoid nodular transformation of the spleen
  • Splenic neoplasms
  • Surgery

ASJC Scopus subject areas

  • Histology
  • Oncology

Cite this