Literature DB >> 27607171

High Uptake of FDG Along a Biliary Stent.

Yasunari Nagasaki1, Hiromichi Yamane, Nobuaki Ochi, Yoshihiro Honda, Nagio Takigawa.   

Abstract

A 66-year-old woman presented with abdominal discomfort. Contrast-enhanced CT revealed a mass in the pancreas and multiple liver metastases. Pathological examination confirmed the mass to be primary pancreatic cancer. Endoscopic insertion of a biliary stent was performed to prevent common bile duct obstruction. Subsequently, she received combination chemotherapy, which resulted in a complete response. FDG-PET-CT after chemotherapy revealed a high uptake of FDG along the outline of the biliary stent, with complete disappearance of both the primary and metastatic tumors.

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Year:  2016        PMID: 27607171      PMCID: PMC5065055          DOI: 10.1097/RLU.0000000000001357

Source DB:  PubMed          Journal:  Clin Nucl Med        ISSN: 0363-9762            Impact factor:   7.794


A, A 66-year-old woman presented with abdominal discomfort. Contrast-enhanced computed tomography (CT) revealed a mass in her pancreas, with multiple liver metastases. Fine-needle aspiration biopsy during endoscopic retrograde cholangiopancreatography confirmed primary pancreatic cancer. B, Endoscopic insertion of a metallic biliary stent was performed to prevent common bile duct obstruction. Subsequently, she received 12 cycles of combination chemotherapy consisting of folic acid, bolus and continuous 5-fluorouracil, irinotecan, and oxaliplatin (FOLFIRINOX),[1] which resulted in a complete response. FDG-PET-CT after chemotherapy revealed a high uptake of FDG along the outline of the biliary stent, with complete disappearance of both the primary and metastatic tumors. FDG-PET is useful for detecting inflammatory biliary and pancreatic diseases, including cancer.[2-4] Typically, FDG-PET-CT has a high sensitivity for detecting cholangiocarcinoma or pancreatic diseases, including malignant neoplasm, and a negative scan indicates a nonmalignant state of disease, even if there is the presence of a small tumor.[2,4,5] However, in the case of nonmalignant disease—for example, autoimmune pancreatitis, including IgG4-related autoimmune pancreatitis, and autoimmune cholangitis—it has been reported that FDG uptake was increased in diseased regions.[2,3,6] In the present case, the finding of a high FDG uptake clearly indicates the outline of the biliary stent without any evidence of cancer involvement. Furthermore, cancer involvement was not shown pathologically after repeated endoscopic examinations.[7] We suspect that this radiological finding may be related to the endoscopic procedure of biliary stent insertion, the major cause being the focal inflammation surrounding the metallic stent.[8] The rate of complete remission (CR) among patients with advanced pancreatic cancer who are treated with FOLFIRINOX is approximately 0.6%.[1] In general, biliary tract cancer and pancreatic cancer have a poor prognosis and are thought to be one of the most intractable malignant tumors. The reported rate of CR of advanced biliary tract cancer is only 2% of patients who are treated with combined chemotherapy consisting of gemcitabine and oxaliplatin.[9] We suggest that residual high uptake of FDG along the biliary stent can be considered to be caused by local inflammation if the initial tumors have been cured by chemotherapy and complete remission has been achieved. Physicians should be aware of this phenomenon because these findings make adequate diagnosis of these cancers difficult. Detailed observation of the clinical course and repetition of the radiological and pathological examinations might help swift and correct diagnosis.
  9 in total

1.  Cetuximab, gemcitabine, and oxaliplatin in patients with unresectable advanced or metastatic biliary tract cancer: a phase 2 study.

Authors:  Birgit Gruenberger; Johannes Schueller; Ute Heubrandtner; Fritz Wrba; Dietmar Tamandl; Klaus Kaczirek; Rudolf Roka; Sandra Freimann-Pircher; Thomas Gruenberger
Journal:  Lancet Oncol       Date:  2010-11-09       Impact factor: 41.316

2.  Biliary tract FDG uptake secondary to stent placement.

Authors:  Eugene C Lin; Matthew Studley
Journal:  Clin Nucl Med       Date:  2003-04       Impact factor: 7.794

3.  FOLFIRINOX versus gemcitabine for metastatic pancreatic cancer.

Authors:  Thierry Conroy; Françoise Desseigne; Marc Ychou; Olivier Bouché; Rosine Guimbaud; Yves Bécouarn; Antoine Adenis; Jean-Luc Raoul; Sophie Gourgou-Bourgade; Christelle de la Fouchardière; Jaafar Bennouna; Jean-Baptiste Bachet; Faiza Khemissa-Akouz; Denis Péré-Vergé; Catherine Delbaldo; Eric Assenat; Bruno Chauffert; Pierre Michel; Christine Montoto-Grillot; Michel Ducreux
Journal:  N Engl J Med       Date:  2011-05-12       Impact factor: 91.245

4.  Brush cytology for pancreatic carcinoma: an analysis of factors influencing results.

Authors:  D E McGuire; R P Venu; R D Brown; K P Etzkorn; W R Glaws; A Abu-Hammour
Journal:  Gastrointest Endosc       Date:  1996-09       Impact factor: 9.427

5.  Usefulness of dual-phase 18F-FDG PET/CT for diagnosing small pancreatic tumors.

Authors:  Natsuko Kawada; Hiroyuki Uehara; Takuya Hosoki; Motohisa Takami; Hisakazu Shiroeda; Tomiyasu Arisawa; Yasuhiko Tomita
Journal:  Pancreas       Date:  2015-05       Impact factor: 3.327

6.  FDG-PET/CT Manifestation of Tumor Seeding Along Percutaneous Biliary Drainage Catheter Tract.

Authors:  Darshan Patel; Yang Lu
Journal:  Clin Nucl Med       Date:  2015-10       Impact factor: 7.794

7.  The value of F-18 FDG PET in patients with primary sclerosing cholangitis and cholangiocarcinoma using visual and semiquantitative analysis.

Authors:  Khaled Alkhawaldeh; Stephanie Faltten; Hans-J Biersack; Samer Ezziddin
Journal:  Clin Nucl Med       Date:  2011-10       Impact factor: 7.794

8.  Autoimmune pancreatitis: whole-body 18F-FDG PET/CT findings.

Authors:  Jian Zhang; Chengwei Shao; Jianhua Wang; Chao Cheng; Changjing Zuo; Gaofeng Sun; Bin Cui; Aisheng Dong; Qinghua Liu; Lingshan Kong
Journal:  Abdom Imaging       Date:  2013-06

9.  Utility of FDG-PET/CT in the diagnosis of IgG4-related diseases.

Authors:  Zheng Zhao; Yanyan Wang; Zhiwei Guan; Jingyu Jin; Feng Huang; Jian Zhu
Journal:  Clin Exp Rheumatol       Date:  2016-02-02       Impact factor: 4.473

  9 in total

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