Literature DB >> 16028441

Mucin-producing cholangiocarcinoma: clinical experience of 24 cases in 16 years.

Chung-Mou Kuo1, Chi-Sin Changchien, Keng-Liang Wu, Seng-Kee Chuah, King-Wah Chiu, Yi-Chun Chiu, Yeh-Pin Chou, Chung-Huang Kuo.   

Abstract

OBJECTIVE: Mucin-producing cholangiocarcinoma (MPCC) is an uncommon biliary tract malignancy. This retrospective study was designed to investigate the clinical presentations, associated diseases, the value of tumor markers, and treatment and prognosis of MPCC.
MATERIAL AND METHODS: The study included 24 MPCC cases (7 M, 17 F) from 132 histopathology-proven cholangiocarcinoma patients seen between 1988 and 2003. MPCC and non-mucin-producing cholangiocarcinoma (non-MPCC) were compared.
RESULTS: Common clinical symptoms and signs included epigastric or right upper quadrant pain, fever and chills, jaundice, and anemia. Seventeen patients had mucobilia in surgical, cholangiographic, or CT findings. Biliary stones were found in 71% of MPCC patients. In detecting MPCC, a serum CA-19-9 level > 120 U/ml had 73% sensitivity, 41% specificity, 25% positive predictive value, 85% negative predictive value, and 48% accuracy in the 132 cholangiocarcinoma patients. The 1-, 2-, 3-, 4-, and 5-year survival rates were 44.3%, 33.8%, 28.1%, 21.1%, and 21.1%, respectively. Univariate analysis showed that tumor type (MPCC) was the only significant factor predicting survival when compared with non-MPCC patients in 5-year cumulative survival rates (21.1% versus 5.4%). MPCC patients receiving surgical resection had a prolonged median survival time (13 months versus 6 months) than those without resection.
CONCLUSIONS: MPCC clinical presentations were similar to non-MPCC in Taiwan except for more jaundice, fever and chills. The major factor predisposing to MPCC was biliary stones. Using serum CA19-9 levels greater than 120 U/ml was a diagnostic aid to detecting MPCC patients. MPCC patients had a better prognosis than non-MPCC patients. The recommended treatment for MPCC is surgical resection.

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Year:  2005        PMID: 16028441     DOI: 10.1080/00365520510011551

Source DB:  PubMed          Journal:  Scand J Gastroenterol        ISSN: 0036-5521            Impact factor:   2.423


  5 in total

1.  Haemostatic radiation therapy for a bleeding intraductal papillary neoplasm of the biliary tree.

Authors:  Senthil Sundaravadanan; Manu Mathew; Thomas Samuel Ram; Philip Joseph
Journal:  BMJ Case Rep       Date:  2018-12-14

2.  A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene.

Authors:  M Vernez; P Hutter; C Monnerat; N Halkic; O Gugerli; H Bouzourene
Journal:  Fam Cancer       Date:  2007       Impact factor: 2.375

3.  Thread sign in biliary intraductal papillary mucinous neoplasm: a novel specific finding for MRI.

Authors:  Gil-Sun Hong; Jae Ho Byun; Jin Hee Kim; Hyoung Jung Kim; Seung Soo Lee; Seung-Mo Hong; Moon-Gyu Lee
Journal:  Eur Radiol       Date:  2015-12-22       Impact factor: 5.315

4.  Diagnosis of cholangiocarcinoma.

Authors:  B E Van Beers
Journal:  HPB (Oxford)       Date:  2008       Impact factor: 3.647

Review 5.  Intraductal papillary neoplasms of the bile duct.

Authors:  Masayuki Ohtsuka; Hiroaki Shimizu; Atsushi Kato; Hideyuki Yoshitomi; Katsunori Furukawa; Toshio Tsuyuguchi; Yuji Sakai; Osamu Yokosuka; Masaru Miyazaki
Journal:  Int J Hepatol       Date:  2014-05-18
  5 in total

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