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   <ui>1754-9493-3-23</ui>
   <ji>1754-9493</ji>
   <fm>
      <dochead>Case report</dochead>
      <bibl>
         <title>
            <p>Management of synchronous adenocarcinoma of the esophago-gastric junction and ampulla of Vater: case report of a surgically challenging condition</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Jayaprakash</snm>
               <fnm>Namita</fnm>
               <insr iid="I1"/>
               <email>namita.jayaprakash@gmail.com</email>
            </au>
            <au id="A2">
               <snm>O'Kelly</snm>
               <fnm>Fardod</fnm>
               <insr iid="I1"/>
               <email>fokelly@rcsi.ie</email>
            </au>
            <au id="A3">
               <snm>Lim</snm>
               <mnm>Tian</mnm>
               <fnm>Kheng</fnm>
               <insr iid="I1"/>
               <email>ktianlim@rcsi.ie</email>
            </au>
            <au ca="yes" id="A4">
               <snm>Reynolds</snm>
               <mnm>Vincent</mnm>
               <fnm>John</fnm>
               <insr iid="I1"/>
               <email>reynoljv@tcd.ie</email>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Clinical Surgery, Trinity Centre, Trinity College Dublin and St James's Hospital, Dublin 8, Ireland</p>
            </ins>
         </insg>
         <source>Patient Safety in Surgery</source>
         <issn>1754-9493</issn>
         <pubdate>2009</pubdate>
         <volume>3</volume>
         <issue>1</issue>
         <fpage>23</fpage>
         <url>http://www.pssjournal.com/content/3/1/23</url>
         <xrefbib>
            <pubidlist>
               <pubid idtype="doi">10.1186/1754-9493-3-23</pubid>
               <pubid idtype="pmpid">19785744</pubid>
            </pubidlist>
         </xrefbib>
      </bibl>
      <history>
         <rec>
            <date>
               <day>27</day>
               <month>6</month>
               <year>2009</year>
            </date>
         </rec>
         <acc>
            <date>
               <day>28</day>
               <month>9</month>
               <year>2009</year>
            </date>
         </acc>
         <pub>
            <date>
               <day>28</day>
               <month>9</month>
               <year>2009</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2009</year>
         <collab>Jayaprakash et al; licensee BioMed Central Ltd.</collab>
         <note>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</note>
      </cpyrt>
      <abs>
         <sec>
            <st>
               <p>Abstract</p>
            </st>
            <p>We report herein a case of a synchronous presentation of an adenocarcinoma of esophagago-gastric junction type II and an ampullary tumor that was treated by combined Whipple's pancreaticoduodenectomy, total gastrectomy and esophagectomy. The magnitude of this operation was safely achieved with meticulous surgical techniques and perioperative care without any major short or long term complications. Patient returned to a good quality of life at six-month follow up with no further gastrointestinal symptoms or evidence of disease recurrence.</p>
         </sec>
      </abs>
   </fm>
   <bdy>
      <sec>
         <st>
            <p>Background</p>
         </st>
         <p>There has been an increase in the West in recent years of adenocarcinoma of the esophagus and esophagago-gastric junction. Standard work-up in high volume centers includes computed tomography (CT) scan, endoscopic ultrasound scan (EUS) and [<sup>18</sup>F]-2-fluoro-2-deoxy-D-glucose-positron emission tomography (<sup>18</sup>F-FDG-PET) imaging. Adenocarcinoma of the esophago-gastric junction (AEG) is classified as per Siewert et al. into AEG type I, arising in the distal esophagus usually on a background of Barrett's esophagus, AEG type II which arises at the anatomic cardia, and AEG Type III tumors are sub-cardial gastric carcinomas which invade the junction and lower esophagus from below <abbrgrp><abbr bid="B1">1</abbr><abbr bid="B2">2</abbr></abbrgrp>. The surgical approach to AEG type I tumors most usually involves a transthoracic esophagectomy with abdominal and mediastinal lymphadenectomy. For AEG type II and III, a total gastrectomy and transmediastinal lymphadenectomy and distal esophagectomy is increasingly utilized <abbrgrp><abbr bid="B3">3</abbr></abbrgrp>. Multimodal approaches, either chemotherapy alone or combined with radiation therapy prior to surgery are increasingly considered for patients with locally advanced disease <abbrgrp><abbr bid="B4">4</abbr></abbrgrp>. The best 5-year survival for surgery for localized AEG tumors is approximately 40 per cent <abbrgrp><abbr bid="B5">5</abbr></abbrgrp>.</p>
         <p>Ampullary cancers, unlike pancreatic carcinomas, may present at an early stage. The goal of surgical management, as in all tumors, remains removal of all gross and microscopic disease from the pancreas and draining lymph node basins <abbrgrp><abbr bid="B6">6</abbr></abbrgrp>. The 5-year survival for completely resected localized disease is approximately 40 per cent <abbrgrp><abbr bid="B7">7</abbr></abbrgrp>.</p>
         <p>In this high volume esophageal (50-80 resections/year) and middle volume pancreatic center (8-15 Whipples/year) a routine work up of a patient with AEG type II junctional tumor uncovered a synchronous ampullary tumor. The case and management considerations are discussed herein.</p>
      </sec>
      <sec>
         <st>
            <p>Case Presentation</p>
         </st>
         <p>A 62 year old man was referred to our service in 2008 with a history of epigastric pain and melaena of one week duration. An upper gastro-intestinal endoscopy revealed an AEG type II junctional tumour (Figure <figr fid="F1">1</figr>). Biopsies revealed an invasive moderately differentiated adenocarcinoma.</p>
         <fig id="F1">
            <title>
               <p>Figure 1</p>
            </title>
            <caption>
               <p>An upper gastrointestinal endoscopy showed irregular AGE Type II junctional tumour with a tongue of Barrett's esophagus</p>
            </caption>
            <text>
               <p><b>An upper gastrointestinal endoscopy showed irregular AGE Type II junctional tumour with a tongue of Barrett's esophagus</b>.</p>
            </text>
            <graphic file="1754-9493-3-23-1"/>
         </fig>
         <p>In routine blood tests his liver function tests were noted to be abnormal, with an AST of 25 IU/L and alkaline phosphatase of 201 IU/L. Endoscopic ultrasound revealed a uT2N0 tumor at the cardia, with one indeterminate peritumoral node. There was also significant dilatation of the common bile duct (CBD) at the duodenal ampulla and major pancreatic duct (MPD) (Figure <figr fid="F2">2</figr>). An intra-ampullary homogenous tumor was identified confined to the ampulla of Vater (Figure <figr fid="F3">3</figr>). CT imaging revealed no evidence of either an esophageal or ampullary tumor, but there was a double-duct sign of biliary and pancreatic duct dilatation (Figure <figr fid="F4">4</figr>). <sup>18</sup>F-FDG-PET imaging revealed no abnormal uptake. Endoscopic Retrograde Cholangiopancreatography (ERCP) revealed a tumor with a large distorted ampulla (Figure <figr fid="F5">5</figr>) and biopsies revealed high grade dysplasia and intra mucosal carcinoma.</p>
         <fig id="F2">
            <title>
               <p>Figure 2</p>
            </title>
            <caption>
               <p>EUS demonstrated significant dilatation of both the CBD (12 mm in diameter) and MPD (7 mm in distal portion)</p>
            </caption>
            <text>
               <p><b>EUS demonstrated significant dilatation of both the CBD (12 mm in diameter) and MPD (7 mm in distal portion)</b>.</p>
            </text>
            <graphic file="1754-9493-3-23-2"/>
         </fig>
         <fig id="F3">
            <title>
               <p>Figure 3</p>
            </title>
            <caption>
               <p>EUS demonstrated a 12 mm homogeneous ampullary tumour with no significant loco-regional nodes</p>
            </caption>
            <text>
               <p><b>EUS demonstrated a 12 mm homogeneous ampullary tumour with no significant loco-regional nodes</b>.</p>
            </text>
            <graphic file="1754-9493-3-23-3"/>
         </fig>
         <fig id="F4">
            <title>
               <p>Figure 4</p>
            </title>
            <caption>
               <p>Abdominal Computed Tomography showed the double duct sign</p>
            </caption>
            <text>
               <p><b>Abdominal Computed Tomography showed the double duct sign</b>.</p>
            </text>
            <graphic file="1754-9493-3-23-4"/>
         </fig>
         <fig id="F5">
            <title>
               <p>Figure 5</p>
            </title>
            <caption>
               <p>Endoscopic view during ERCP showed a large ampullary tumour</p>
            </caption>
            <text>
               <p><b>Endoscopic view during ERCP showed a large ampullary tumour</b>.</p>
            </text>
            <graphic file="1754-9493-3-23-5"/>
         </fig>
         <p>The patient had good overall performance status. He had a background history of insulin dependent diabetes mellitus with secondary complications including retinopathy and peripheral neuropathy. His HbA1c on admission was 8.0 g/dL. He also had a history of ischemic heart disease with subsequent angioplasty in 2006. He had hypertension, diverticular disease and colonic polyps. A pre-operative exercise stress test and ECHO revealed good functional capacity with an ejection fraction of 60-65%. His FEV1 was 2.37 litres and his FVC was 4.30 litres. Pre-assessment by the anaesthetist, cardiologist and endocrinologist certified patient fit for major operation.</p>
         <p>The decision was made to proceed to synchronous resections with a planned Whipple's, total gastrectomy and distal esophagectomy, mediastinal dissection and Roux-en-Y esophago-jejunal reconstruction in that order respectively via the upper midline laparotomy incision. There was no technical difficulties in reconstructing the four anastomoses namely hepatico-jejunostomy, pancreatico-jejunostomy, esophago-jejunostomy and jejuno-jejunostomy (Figure <figr fid="F6">6</figr>). The operation was uneventful, taking 340 minutes, the blood loss was 620 mls, and he was extubated immediately postoperatively. The patient spent 10 days post operatively in the High Dependency Unit (HDU). Analgesia was provided via an epidural at the level of T7/T8 and the patient was given total parenteral nutrition (TPN). He experienced no major complications and was discharged home 22 days postoperatively.</p>
         <fig id="F6">
            <title>
               <p>Figure 6</p>
            </title>
            <caption>
               <p>A drawing illustrating the liver (L), pancreas (P), hepatico-jejunostomy (H-J), pancreatico-jejunostomy (P-J), esophago-jejunostomy (E-J) and jejuno-jejunostomy (J-J) anastomoses</p>
            </caption>
            <text>
               <p><b>A drawing illustrating the liver (L), pancreas (P), hepatico-jejunostomy (H-J), pancreatico-jejunostomy (P-J), esophago-jejunostomy (E-J) and jejuno-jejunostomy (J-J) anastomoses</b>.</p>
            </text>
            <graphic file="1754-9493-3-23-6"/>
         </fig>
         <p>Histology of the junctional tumor revealed a 6 mm tumor, pT1 N0 Mx, with 0 out of 16 nodes involved and negative margins. The ampullary tumor was invasive adenocarcinoma, pT1 N0 Mx, and 0 out of 7 nodes were involved. No adjuvant therapy is being considered. Patient returned to a good quality of life at six-month follow up with no further gastrointestinal symptoms or evidence of disease recurrence.</p>
      </sec>
      <sec>
         <st>
            <p>Discussion</p>
         </st>
         <p>Synchronous presentation of esophago-gastric and peri-ampullary adenocarcinoma is extremely rare. In a study by Lee et al., 3.4% of gastric cancers were associated with synchronous tumors, most commonly colorectal cancer <abbrgrp><abbr bid="B7">7</abbr></abbrgrp>. Another review of 10,090 patients with gastric cancer reported that 96 had synchronous tumors and 5 of those were pancreatic carcinoma <abbrgrp><abbr bid="B8">8</abbr></abbrgrp>. The management of a case of squamous cell carcinoma (SCC) of the esophagus with an intraductal pancreatic polypoid tumor has been reported, as well as a case of SCC of the esophagus with adenocarcinoma of the ampulla of Vater <abbrgrp><abbr bid="B9">9</abbr><abbr bid="B10">10</abbr></abbrgrp>. There was a report on technical challenges in avoiding injury to the middle colic vessels with successful pancreaticoduodenectomy for carcinoma of the ampulla of Vater after esophagectomy with remnant gastrectomy 17 years prior <abbrgrp><abbr bid="B11">11</abbr></abbrgrp>. To our knowledge there is no reported case of synchronous adenocarcinoma of the esophago-gastric junction and ampullary adenocarcinoma.</p>
         <p>For both tumors independently, surgical resection is the only curative approach, and the risk of mortality for each procedure should be less than 5 per cent in high-volume centers. Neoadjuvant chemotherapy or chemoradiotherapy for AEG type II junctional adenocarcinoma was discussed but not pursued since this appeared localized and node-negative with a high probability of an R0 resection <abbrgrp><abbr bid="B12">12</abbr></abbrgrp>. The role of perioperative chemotherapy based on MAGIC trial probably offer little benefit in altering resectability, progression-free survival and overall survival of this early stage AEG type II junctional tumour <abbrgrp><abbr bid="B13">13</abbr></abbrgrp>. The risk of adverse effects of haematological and non-haematological toxicity associated with perioperative chemotherapy was considered and discussed.</p>
         <p>The surgical treatment options considered in our patient were combined Whipple's pancreaticoduodenectomy, total gastrectomy, distal esophagectomy and Roux-en-Y esophago-jejunal reconstruction along with hepatico-jejunostomy, pancreatico-jejunostomy and jejuno-jejunostomy. We were prepared to do a thoracotomy to get adequate clearance if required, but splitting the diaphragm and a mediastinal dissection and anastomosis were achievable via the abdominal incision. Increasing evidence supports the rationale to avoid transthoracic surgery for AEG type II tumors which are predominantly of gastric origin and rarely involve high mediastinal or sub-carinal nodes <abbrgrp><abbr bid="B1">1</abbr><abbr bid="B3">3</abbr></abbrgrp>.</p>
         <p>For the ampulla, the EUS and ERCP were more in keeping with an invasive rather than an in situ cancer, and a local resection was not considered. A pylorus -preserving approach with gastric preservation combined with a proximal gastrectomy and esophagectomy would have been technically possible, but functional results from total gastrectomy with Roux-en-Y esophago-jejunal reconstruction may be better due to the risk of reflux esophagitis. There appears to be only one previous report in the literature of a similar procedure for synchronous tumors. Mafune et al. described a case of subtotal esophagectomy for SCC, pancreaticoduodenectomy with lymph node dissection and total residual gastrectomy in a patient who had a previous gastrectomy <abbrgrp><abbr bid="B10">10</abbr></abbrgrp>.</p>
         <p>Synchronous resection of AEG type II junctional tumour and ampullary tumour appears attractive although it takes longer to perform, the benefits are having one general anaesthesia for four anastomotic reconstructions and thus avoiding a second major operation. Whilst a staged procedure may take shorter to perform, the risks are two general anesthesia with potential adhesions complicating second stage procedure and the potential delay in resection of second rapidly progressing tumour. Suzuki et al. reported simultaneous resection of synchronous esophageal and extraesophageal carcinomas can be safely performed with no significant difference in morbidity and mortality compared to solitary esophageal cancer resection as long as complete clearance of both tumours is achieved for favourable long-term results <abbrgrp><abbr bid="B14">14</abbr></abbrgrp>.</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>This is the first report of combined Whipple's and esophago-gastrectomy for these synchronous tumors. The magnitude of this operation was safely achieved with meticulous surgical techniques and perioperative care without any major complications.</p>
      </sec>
      <sec>
         <st>
            <p>Consent</p>
         </st>
         <p>Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.</p>
      </sec>
      <sec>
         <st>
            <p>Competing interests</p>
         </st>
         <p>The authors declare that they have no competing interests.</p>
      </sec>
      <sec>
         <st>
            <p>Authors' contributions</p>
         </st>
         <p>NJ and FO drafted the manuscript. KTL prepared the figures, reviewed and amended and finalized the manuscript. JVR critically reviewed, amended and finalized the manuscript. All authors read and approved the final manuscript.</p>
      </sec>
   </bdy>
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