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DOI: 10.1055/s-0032-1325888
A case of mucinous cystadenocarcinoma of the pancreas with spontaneous rupture diagnosed by endoscopic retrograde pancreatography
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Publication History
Publication Date:
22 March 2013 (online)
Mucinous cystic neoplasm (MCN) of the pancreas is characterized by a multilocular cystic lesion lined by mucin-producing columnar epithelium and an ovarian-type stroma [1]. MCNs are often found incidentally and may occasionally cause symptoms. Rupture of a pancreatic MCN is a rare complication, and only a few cases have been reported to date [2] [3] [4] [5]. Many of these cases occurred during pregnancy [2] [3] [5]. This report is the first to describe a case of ruptured MCN with an associated invasive carcinoma of the pancreas diagnosed by endoscopic retrograde pancreatography (ERP).
In a 69-year-old woman complaining of abdominal pain, contrast-enhanced computed tomography (CT) showed a low-density mass 60 mm in diameter that communicated with a dilated main pancreatic duct ([Fig. 1]). Contrast-enhanced endoscopic ultrasound (EUS) revealed a mixed-echo pattern in the mass and enhancement effects in hyperechoic areas ([Fig. 2]). The findings on CT, EUS, and magnetic resonance imaging (not shown) suggested that the tumor was a multilocular cystic lesion of the pancreas with solid components, but they were atypical, and a diagnosis could not be reached. ERP was then performed and showed leakage of contrast medium from the main pancreatic duct into the peritoneal cavity ([Fig. 3]). CT images obtained immediately after ERP showed pooling of contrast medium in the peritoneal cavity around the tumor ([Fig. 4]). A body-tail pancreatectomy with splenectomy was performed quasi-emergently 5 days after ERP. The definitive pathological diagnosis was mucinous cystadenocarcinoma of the pancreas with foci of ovarian-like stroma ([Fig. 5]). After surgery, the patient underwent chemotherapy with 5-fluorouracil and has remained symptom-free, with no detectable tumor recurrence at present, 2 months after surgery.










To the best of our knowledge, this is the first report of MCN of the pancreas with spontaneous rupture diagnosed by ERP.
Endoscopy_UCTN_Code_CCL_1AZ_2AB
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Competing interests: None
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References
- 1 Brugge WR, Lauwers GY, Sahani D et al. Cystic neoplasms of the pancreas. N Engl J Med 2004; 351: 1218-1226
- 2 Naganuma S, Honda K, Noriki S et al. Ruptured mucinous cystic neoplasm with an associated invasive carcinoma of pancreatic head in a pregnant woman: report of a case and review of literature. Pathol Int 2011; 61: 28-33
- 3 Ozden S, Haliloglu B, Ilter E et al. An extremely rare cause of acute abdomen in pregnancy: ruptured pancreatic mucinous cystadenocarcinoma. Pancreas 2007; 34: 474-476
- 4 Bergenfeldt M, Poulsen IM, Hendel HW et al. Pancreatic ascites due to rupture of a mucinous cystic neoplasm. Acta Oncol 2008; 47: 978-981
- 5 Smithers BM, Welch C, Goodall P. Cystadenocarcinoma of the pancreas presenting in pregnancy. Br J Surg 1986; 73: 591
Corresponding author
-
References
- 1 Brugge WR, Lauwers GY, Sahani D et al. Cystic neoplasms of the pancreas. N Engl J Med 2004; 351: 1218-1226
- 2 Naganuma S, Honda K, Noriki S et al. Ruptured mucinous cystic neoplasm with an associated invasive carcinoma of pancreatic head in a pregnant woman: report of a case and review of literature. Pathol Int 2011; 61: 28-33
- 3 Ozden S, Haliloglu B, Ilter E et al. An extremely rare cause of acute abdomen in pregnancy: ruptured pancreatic mucinous cystadenocarcinoma. Pancreas 2007; 34: 474-476
- 4 Bergenfeldt M, Poulsen IM, Hendel HW et al. Pancreatic ascites due to rupture of a mucinous cystic neoplasm. Acta Oncol 2008; 47: 978-981
- 5 Smithers BM, Welch C, Goodall P. Cystadenocarcinoma of the pancreas presenting in pregnancy. Br J Surg 1986; 73: 591









