Case Report
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World J Gastroenterol. Jan 28, 2011; 17(4): 540-542
Published online Jan 28, 2011. doi: 10.3748/wjg.v17.i4.540
Isolated pancreatic granulocytic sarcoma: A case report and review of the literature
Xin-Ping Li, Wen-Fang Liu, Shu-Rong Ji, She-Hua Wu, Jian-Jun Sun, Yue-Zu Fan
Xin-Ping Li, Wen-Fang Liu, Shu-Rong Ji, She-Hua Wu, Jian-Jun Sun, Yue-Zu Fan, Department of Surgery, Tongji Hospital of Tongji University, Shanghai 200065, China
Author contributions: Li XP and Liu WF contributed equally to this work; Li XP and Liu WF collected the data and wrote the article; Li XP, Ji SR and Wu SH analyzed the data; Liu WF, Sun JJ and Fan YZ designed the study.
Correspondence to: Dr. Wen-Fang Liu, Department of Surgery, Tongji Hospital of Tongji University, Shanghai 200065, China. lwf112@163.com
Telephone: +86-21-66111082 Fax: +86-21-66111082
Received: August 19, 2010
Revised: November 25, 2010
Accepted: December 1, 2010
Published online: January 28, 2011
Abstract

Granulocytic sarcoma (GS) is an extramedullary tumor mass consisting of immature myeloid cells. Isolated pancreatic granulocyte sarcoma is extremely rare. We report a very unusual pancreatic granulocytic sarcoma in a patient without acute myeloid leukemia. The patient presented with acute epigastric pain because of splenic infarction due to a mass consisting of myeloblasts in the pancreatic tail. The patients underwent splenectomy and distal pancreatectomy. Pathology and immunohistochemistry suggested a GS. Despite local surgery, an isolated tumor recurred 2 mo after operation and the patient died 3 mo after removal of the tumor. Only 7 reported cases of pancreatic GS were identified in the literature and the mass was located in the pancreatic head. This is the first report of GS in the pancreatic tail with splenic infarction.

Keywords: Granulocytic sarcoma, Pancreatic mass