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Sentinel node biopsy during thoracolaparoscopic esophagectomy for advanced esophageal cancer
World Journal of Surgical Oncology volume 14, Article number: 117 (2016)
Omitting extensive lymph node dissection could reduce esophagectomy morbidity in patients without lymph node metastases. Sentinel node biopsy may identify abdominal or thoracic lymph node metastases, thereby differentiating treatment. Feasibility of this approach was investigated in Western European esophageal cancer patients with advanced disease, without lymph node metastases at diagnostic work-up.
The sentinel node biopsy was performed in eight esophageal cancer patients with cT1-3N0 disease. One day pre-operatively, Tc-99m-labeled nanocolloid was endoscopically injected around the tumor. Lymphoscintigraphy was performed 1 and 3 h after injection. All patients underwent robotic thoracolaparoscopic esophagectomy with two-field lymph node dissection. Intraoperatively, sentinel nodes were detected by gamma probe. The resection specimen was analyzed for remaining activity by scintigraphy and gamma probe.
Visualization rates of lymphoscintigraphy 1 and 3 h after tracer injection were 88 and 100 %, respectively. Intraoperative identification rate was 38 %. Postoperative identification was possible in all patients using the gamma probe to analyze the resection specimen. In 5/8 patients, lymph node metastases were found at histopathology, none of which was detected by the sentinel node biopsy. No adverse events related to the sentinel node biopsy were observed.
In our advanced esophageal cancer patients who underwent thoracolaparoscopic esophagectomy, the sentinel node biopsy did not predict lymph node status. Probably the real sentinel node could not be identified due to localization adjacent to the primary tumor or bypassing due to metastatic tumor involvement. Therefore, we consider the sentinel node biopsy not feasible in advanced esophageal cancer.
Esophageal cancer is the eighth most common malignancy in the world affecting more than 450,000 people worldwide, and the incidence is rapidly increasing . For patients with locoregional disease, the best chance for cure is offered by radical esophagectomy . As the esophagus has a unique submucosal lymphatic drainage system, the lymphatic spread of esophageal cancer is unpredictable and highly variable . For example, the prevalence of cervical lymph node metastases in patients with gastroesophageal junction tumors and those with tumors in the distal third of the esophagus is 17 and 23 %, respectively .
Current staging modalities have limited predictive value for lymphatic involvement in esophageal cancer patients. Regional lymph node status is mainly defined by computed tomography (CT) and 18F-fluorodeoxyglucose positron emission tomography (FDG-PET), or combined FDG-PET/CT . However, suboptimal imaging quality often leads to incorrect assessment of locoregional tumor extent . Therefore, during transthoracic esophagectomy (TTE), an extensive mediastinal and upper abdominal lymph node dissection (LND) is always performed to clear all possible metastatic disease. As the cervical region is a common site of tumor recurrence, some surgeons routinely perform a cervical LND as well [4, 6, 7].
The transthoracic extensive mediastinal lymph node dissection is accompanied by substantial cardiopulmonary morbidity . Surgical strategies such as a transhiatal approach and minimally invasive techniques have been employed to reduce the morbidity [8, 9]. For patients without lymph node metastases in the resected specimen (pN0), the extensive LND of TTE may be regarded redundant. In these patients, morbidity could be reduced by tailoring the extent of LND. This could be accomplished by the application of sentinel node navigation surgery.
A sentinel node (SN) is defined as the lymph node that receives lymphatic flow directly from the primary tumor, being the first site of metastatic spread . Depending on the tracer used, SNs can be detected by a gamma camera, a gamma probe, CT lymphography, magnetic resonance imaging (MRI) lymphography, or by observing blue dye. The SN concept states that when pathologic analysis of the detected SN(s) shows no tumor invasion, extensive dissection of the lymph nodes that drain the SN(s) can be omitted . SN biopsy is now widely adopted in the management of early stage breast cancer and melanoma [11–13].
In esophageal cancer, SN mapping by radioactive tracer was first described by Kitagawa et al. in 2000 . In subsequent years, several other clinical studies on this subject have been performed, predominantly in Japanese institutes [15–19].
The aim of the current study was to assess the feasibility and safety of SN mapping in Western European esophageal cancer patients during minimally invasive thoracolaparoscopic esophagectomy.
A total of eight patients with resectable esophageal cancer who were scheduled to undergo esophagectomy with two-field LND were included in our feasibility study. Routine diagnostic work-up consisted of esophagogastroduodenoscopy (EGD) with biopsy, radial endoscopic ultrasonography (EUS) (GIF-UM130, Olympus, Hamburg, Germany), CT scan of the chest and abdomen, ultrasonography (US) of the neck with fine needle aspiration (FNA) when indicated, and lung function testing and bronchoscopy in case of suspected airway ingrowth. Patients were eligible for SN biopsy if all of the following criteria were fulfilled: (i) proven adenocarcinoma (AC) or squamous cell carcinoma (SCC) of the esophagus; (ii) resectable disease (i.e., cT1-3 or cT4pleura/crus); (iii) no pre-operative evidence of lymph node metastases (cN0, cM0); and (iv) no neoadjuvant therapy.
Radiocolloid injection and pre-operative SN identification
One day before surgery patients underwent EGD under light sedation. Using a 9.8-mm gastroscope (GIF-140, Olympus, Hamburg, Germany), 400 MBq Tc-99m-labeled nanocolloid (Amersham Cygne, Eindhoven, The Netherlands) in a maximum volume of 2 mL was injected into the submucosal layer overlaying the tumor in four quadrants (two proximal and two distal from the tumor; Fig. 1).
One hour and approximately 3 h after injection, static images in the anterior, posterior, and lateral planes were obtained by a dual-head gamma camera with a low-energy, high-resolution (LEHR) collimator (Argus®; Philips Medical Systems, Best, The Netherlands) to locate focal areas of radioactivity (Figs. 2 and 3).
Surgical procedure and intraoperative SN identification
All patients underwent thoracolaparoscopic esophagectomy with two-field LND aided by the Da Vinci™ robotic system (Intuitive Surgical, Sunnyvale, USA) . Dissected lymph nodes included the paratracheal, subcarinal, aortopulmonary window, peri-esophageal, celiac, and lesser omental nodes. The digestive tract was reconstructed by a gastric conduit, which was anastomosed in the neck.
During surgery, potential SNs in the thoracic and abdominal cavities were identified by a laparoscopic handheld gamma probe (Europrobe II; Eurorad, Strasbourg, France). Radioactivity of the cervical region was assessed with the handheld gamma probe through the cervical incision at the left side and percutaneously at the right side of the neck. After the resected specimen was removed from the patient, the thoracic and abdominal cavities were explored with the gamma probe for remaining the radioactivity.
Postoperative SN identification
At the Department of Pathology, the resected specimen was opened and was attached on a paraffin board. In this way, overlap in radioactivity from the tumor and from possible lymph nodes was avoided. Lymphoscintigraphy of the resected specimen was performed at the Department of Nuclear Medicine in order to visualize the location of the focal radioactivity; possible SNs were marked. Subsequently, the radioactivity of the detected possible SNs was counted with the handheld gamma probe, and the identified hot nodes were separated from the resected specimen for individual histopathologic examination.
The resected esophageal specimen including the remaining non-sentinel lymph nodes were fixed in 4 % formalin for 24 h. Non-sentinel lymph nodes were identified by slicing the fatty tissue surrounding the esophagus and gastric cardia. The resected specimen and non-SNs, cut in largest diameter, were fixed in formalin and embedded in paraffin. Tissue sections (3 μm) were stained with hematoxylin and eosin (H&E) for routine histopathologic examination. All resected specimens were examined by one experienced oncologic pathologist (MS).
SNs were processed according to a standard protocol. After formalin fixation and paraffin embedding, step sections of 3-μm thick were cut at five levels with 250-μm intervals for H&E staining. When no lymph node metastases could be identified by H&E examination, immunohistochemical analysis was performed at each level with CAM 5.2 (Becton-Dickinson Biosciences, San Jose, USA, catalog# 349205) in case of primary adenocarcinoma or CK AE1/3 (Neomarkers/Lab Vision, Fremont, USA, catalog# MS-343-P) in case of SCC to detect micrometastases or isolated tumor cells.
The median age at the time of surgery was 62 (range, 45–71) years (Table 1). The tumor was located in the middle third part of the esophagus in two (25 %) patients, the lower third in five (63 %) and the gastroesophageal junction in one (13 %). The median tumor size was 3.5 (range, 2–8) cm. Histopathologic examination of the resected specimens revealed that 50 % of the tumors were adenocarcinomas and 50 % were squamous cell carcinomas.
No complications of the SN procedure were noticed. The lymphoscintigraphy performed 1 h after radiocolloid injection identified possible SNs in seven out of eight patients, resulting in a visualization rate of 88 %. A median of two SNs (range 0–4) were detected by the lymphoscintigraphy performed 1 h after injection (Table 1). The visualization rate of lymphoscintigraphy performed 3 h post injection was 100 %, with a median of 3.5 (range 2–7) identified SNs.
Intraoperative SN detection
With the intraoperative gamma probe, the identification rate was 38 % (three patients out of eight). The main cause of failure was the accumulation of the radioactive tracer in the lymph nodes in direct proximity to the tumor, with the tumor radioactivity surpassing the radioactivity of surrounding lymph nodes. In the three patients, a total of five SNs could be detected with the intraoperative gamma probe. These five SNs were detected cervically (n = 3), para-esophageally (n = 1), and subcarinally (n = 1).
SN detection in resected specimen
Scintigraphic examination of the resected specimen revealed a median of five SNs (range 1–5) in all patients. The identification rate was 100 %. When analyzing the resected specimen with the gamma probe, in all eight patients, one or more SN(s) were detected. Therefore, the post-surgical identification rate for the gamma probe was 100 %. A median number of three SNs (range 1–5) were detected by gamma probe analysis of the resected specimens.
In all five patients with lymph node metastases in the resected specimen, the SN was tumor negative even after immunohistochemical analysis and additional serial sectioning.
In our Western European study group of patients with esophageal cancer who underwent minimally invasive thoracolaparoscopic surgery, the SN procedure did not predict lymph node status. Most probably, the sentinel node could not be identified due to close proximity to the tumor, which surpassed the radioactivity of surrounding lymph nodes. In Western European countries, esophageal cancer patients present with advanced disease in the absence of screening programs. Although at clinical work-up, patients seem to be without lymph node metastases, histopathologic examination of the resection specimen reveals lymph node metastases in the majority of patients . Therefore, although our feasibility study contains only a low number of patients, we conclude that the SN procedure is not feasible in patients with advanced esophageal cancer. The complex and vast lymphatic drainage system of the esophagus contributes to the unreliability of the SN procedure. Another contributing factor could be a learning curve of performing the SN procedure during thoracolaparoscopic esophagectomy. Of note, four out of five patients with lymph node metastases had T3 disease. Ovrebo et al. reported lymph node metastases in 74 % of patients with pT3 tumors , which raises the question whether depth of tumor invasion is a better predictor of lymph node involvement than the SN procedure.
Some technical issues deserve more consideration. In our series, lymphoscintigraphy 1 and 3 h after radioactive tracer injection resulted in visualization rates of 88 and 100 %, respectively. The higher rate in the latter is probably due to further flow of tracer particles in the lymphatics, resulting in the appearance of more first echelon lymph nodes. These results exceed those reported in the literature (60–92 %; Table 2), despite the fact that the time between tracer injection and initial lymphoscintigraphy in those studies was longer (range 3–12 h) [17, 23]. This could be explained by the variation in particle size of the radioactive tracers used. As shown in Table 2, the most commonly used tracer in Japan is Tc-99m-labeled stannous colloid [14, 15, 17–19, 23, 24] (particle size 400–500 nm), whereas in the Western world, it is Tc-99m nanocolloid [25–27] (<80 nm). The larger the particle size, the longer it takes to pass through the lymphatic system. However, our SN identification rate is comparable to the pooled SN identification rate with Tc-99m of 0.970, reported in a recently published meta-analysis .
In order to determine the location of the SNs, most research groups produce lymphoscintigraphic images in 1 or 2 planes: the anterior [14, 24, 29–31], posterior, or both [16, 17]. However, due to overprojection of injection sites, it may be difficult to image SNs. In order to increase the yield, we added an oblique plane to the anterior and posterior acquisition planes. Additionally, in the first patient, we performed a single photon emission CT (SPECT) study. Despite these efforts, visualization of peritumoral SNs remained difficult due to massive retention of radioactivity at the injection sites. This may have caused false-negative examinations. Overall, the false negative rate of our study (100 %) is identical to that of Kosugi et al. , but substantially higher than results reported in four other series (4–22 %) [15, 16, 23, 27].
The false negative results could also be caused by metastatic tumor cells. When either the lymphatic drainage channels or the lymph nodes are blocked by tumor cells, the tracer may not be able to enter the initial lymphatic drainage of the tumor and may follow an alternative route, in that way bypassing the SNs. This hypothesis is supported by data from the literature. In 43 patients with esophageal or gastric cancer having undergone SN mapping with 0.75 mCi 99mTc-Sn colloid, radioisotope uptake was significantly decreased in lymph nodes in which more than 60 % of the lymph node contained metastatic tumor cells . Remarkably, when reviewing the current literature on SN biopsy in esophageal cancer, 4 (36 %) of 11 studies included patients with clinical suspicion of lymph node metastases [15, 16, 18, 27]. As this is an indication for extensive LND, SN biopsy in these patients offers no added value. For this reason, our aim was to include only cN0 patients in our feasibility study. Nonetheless, histopathologic examination of the resected specimens revealed lymph node metastases in five (63 %) of eight patients.
Our intraoperative gamma probe detection rate was 38 %. Eight other research groups have attempted to intraoperatively identify SNs with a gamma probe as well (Table 2) [14–16, 19, 23–25, 27]. Lamb et al. reported an intraoperative detection rate of 100 % . An explanation for their excellent results could be the timing of the injected radioactive tracer immediately prior to surgery, which allowed for the identification of early lymphatic spread. Yet, the authors reported no screening for the undetected lymph nodes of the resected specimens (e.g., with a gamma camera). In our opinion, the intraoperative gamma probe is beneficial only in detecting hot nodes in the cervical region and for exploring the abdominal and thoracic cavities for remaining radioactivity after resection. Ex vivo SN identification by means of the gamma probe was possible in all (100 %) patients, which is comparable to the 90–95 % reported in the literature (Table 2) [15, 17]. As lymphoscintigraphy visualizes radioactive tracer accumulation as well as tracer pathways, the actual amount of SNs identified by gamma probe analysis of the resected specimens in our series was less than the number of areas with high amounts of radioactivity as identified by lymphoscintigraphic examination of the resected specimens.
As an alternative for the radionuclide procedure, Suga et al. have developed interstitial CT lymphography to detect SNs [32, 33]. With this technique, the water-soluble iodine contrast medium iopamidol is endoscopically injected into the submucosal layer surrounding the tumor. By multiplanar reconstruction and maximum intensity projection images reconstructed from the transaxial post-contrast CT images, the route of enhanced lymphatic vessels can be visualized. The first lymph nodes with direct connection to these lymphatic vessels are considered the SNs. In 12 patients with superficial esophageal cancer, a median of 2.3 SNs were detected. All pre-operatively detected SNs were identified during surgery. With a sensitivity of 100 % and with no false negative cases, this technique seems promising [32, 33]. In a recent meta-analysis, a pooled detection rate of 0.970, an accuracy of 0.902, and an overall estimated sensitivity of 0.831 were reported for this technique; however, patients with advanced disease were not included . Comparable favorable results of CT lymphography have been obtained in other malignancies, such as lung and breast carcinoma [34–36].
SN mapping could also be done by means of ferumoxide-enhanced MRI lymphography [37–39]. Similar to the two techniques described before, superparamagnetic iron oxide is injected into the submucosa of the peritumoral region during gastroscopy. Overall sensitivity of this procedure was only 66 % (four out of six patients), due to absence of flux of ferumoxides to metastatic lymph nodes in two patients . An additional disadvantage of this technique in esophageal cancer is that cardiac motion artifacts limit the scanning area to the region from the larynx to the carina and from the gastric cardia to the renal hilus . Consequently, peri-esophageal (i.e., regional) lymph nodes, which frequently are the first site of metastatic tumor spread, cannot be assessed. This may cause false negative examinations as well.
Although dye-guided detection of SNs is commonly used in breast cancer and melanoma, it has not gained wide popularity in esophageal cancer. As the lymphatic drainage of the esophagus is unpredictable and variable, real-time observation of the lymphatic pathway of esophageal tumors by blue dye is only feasible when the esophagus is entirely mobilized. This, however, will lead to destruction of the active lymphatic flow from the primary tumor and will compromise the further detection of SNs. Furthermore, it is difficult to differentiate blue colored upper mediastinal lymph nodes from nodes that are pigmented by anthracosis. Additionally, it is impossible to directly follow the lymphatic flow from the primary tumor to cervical lymph nodes. Burian et al. described the application of blue dye in combination with a radioactive tracer in SN mapping for esophageal cancer . Blue dye was easily detected in abdominal lymph nodes during laparotomy of patients with AEG III (subcardial) tumors. In case of distal esophageal or AEG II carcinomas, SNs located in the lower mediastinum could only be detected with the radioactive tracer . In a recent meta-analysis, two studies were included using blue dye as a tracer, resulting in a pooled detection rate of 0.971, an accuracy of 0.790, and a sensitivity of 0.811 .
In the current feasibility study, the SN procedure did not predict lymph node status in Western European esophageal cancer patients who underwent minimally invasive thoracolaparoscopic esophagectomy. The localization of the SN just adjacent to the tumor as well as the complexity of the esophageal lymph node basin are important factors in the unreliability of the SN procedure in esophageal cancer patients, and this technique should therefore be considered not feasible in these patients. However, our results should be confirmed in larger studies.
Ethics approval and consent to participate
The study was approved by our local medical research ethics committee (UMC Utrecht Research Ethics Committee) and has therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki. Written informed consent was obtained from all participating patients prior to their inclusion in the study.
Consent for publication
fine needle aspiration
hematoxylin and eosin
low energy, high resolution
lymph node dissection
magnetic resonance imaging
squamous cell carcinoma
single photon emission CT
Zhang Y. Epidemiology of esophageal cancer. World J Gastroenterol. 2013;19:5598–606.
Hulscher JB, van Sandick JW, de Boer AG, Wijnhoven BP, Tijssen JG, Fockens P, et al. Extended transthoracic resection compared with limited transhiatal resection for adenocarcinoma of the esophagus. N Engl J Med. 2002;347:1662–9.
Zuidema GD, Orringer MB, Ritchie Jr WP, Turcotte JG, Condon RE, Nyhus LM. Shackelford’s surgery of the alimentary tract. Philadelphia: WB Saunders; 1996.
Lerut T, Nafteux P, Moons J, Coosemans W, Decker G, De Leyn P, et al. Three-field lymphadenectomy for carcinoma of the esophagus and gastroesophageal junction in 174 R0 resections: impact on staging, disease-free survival, and outcome: a plea for adaptation of TNM classification in upper-half esophageal carcinoma. Ann Surg. 2004;240:962–72.
van Rossum PS, van Hillegersberg R, Lever FM, Lips IM, van Lier AL, Meijer GJ, et al. Imaging strategies in the management of oesophageal cancer: what’s the role of MRI? Eur Radiol. 2013;23:1753–65.
Isono K, Sato H, Nakayama K. Results of a nationwide study on the three-field lymph node dissection of esophageal cancer. Oncology. 1991;48:411–20.
Baba M, Aikou T, Yoshinaka H, Natsugoe S, Fukumoto T, Shimazu H, et al. Long-term results of subtotal esophagectomy with three-field lymphadenectomy for carcinoma of the thoracic esophagus. Ann Surg. 1994;219:310–6.
Orringer MB, Marshall B, Chang AC, Lee J, Pickens A, Lau CL. Two thousand transhiatal esophagectomies: changing trends, lessons learned. Ann Surg. 2007;246:363–72.
Luketich JD, Alvelo-Rivera M, Buenaventura PO, Christie NA, McCaughan JS, Litle VR, et al. Minimally invasive esophagectomy: outcomes in 222 patients. Ann Surg. 2003;238:486–94.
Nieweg OE, Tanis PJ, Kroon BB. The definition of a sentinel node. Ann Surg Oncol. 2001;8:538–41.
Amersi F, Morton DL. The role of sentinel lymph node biopsy in the management of melanoma. Adv Surg. 2007;41:241–56.
Sato K, Shigenaga R, Ueda S, Shigekawa T, Krag DN. Sentinel lymph node biopsy for breast cancer. J Surg Oncol. 2007;96:322–9.
Kim T, Giuliano AE, Lyman GH. Lymphatic mapping and sentinel lymph node biopsy in early-stage breast carcinoma: a metaanalysis. Cancer. 2006;106:4–16.
Kitagawa Y, Fujii H, Mukai M, Kubota T, Ando N, Watanabe M, et al. The role of the sentinel lymph node in gastrointestinal cancer. Surg Clin North Am. 2000;80:1799–809.
Arima H, Natsugoe S, Uenosono Y, Arigami T, Ehi K, Yanagita S, et al. Area of nodal metastasis and radioisotope uptake in sentinel nodes of upper gastrointestinal cancer. J Surg Res. 2006;135:250–4.
Kato H, Miyazaki T, Nakajima M, Takita J, Sohda M, Fukai Y, et al. Sentinel lymph nodes with technetium-99m colloidal rhenium sulfide in patients with esophageal carcinoma. Cancer. 2003;98:932–9.
Kosugi S, Nakagawa S, Kanda T, Odano I, Yajima K, Kaneko K, et al. Radio-guided sentinel node mapping in patients with superficial esophageal carcinoma: feasibility study. Minim Invasive Ther Allied Technol. 2007;16:181–6.
Tanaka C, Fujii H, Kitagawa Y, Nakahara T, Suzuki T, Tanami Y, et al. Oblique view of preoperative lymphoscintigraphy improves detection of sentinel lymph nodes in esophageal cancer. Ann Nucl Med. 2005;19:719–23.
Yasuda S, Shimada H, Chino O, Tanaka H, Kenmochi T, Takechi M, et al. Sentinel lymph node detection with Tc-99m Tin colloids in patients with esophagogastric cancer. Jpn J Clin Oncol. 2003;33:68–72.
van Hillegersberg R, Boone J, Draaisma WA, Broeders IA, Giezeman MJ, Borel Rinkes IH. First experience with robot-assisted thoracoscopic esophagolymphadenectomy for esophageal cancer. Surg Endosc. 2006;20:1435–9.
Boone J, Schipper ME, Moojen WA, Borel Rinkes IH, Cromheecke GJ, van Hillegersberg R. Robot-assisted thoracoscopic oesophagectomy for cancer. Br J Surg. 2009;96:878–86.
Ovrebo KK, Lie SA, Laerum OD, Svanes K, Viste A. Long-term survival from adenocarcinoma of the esophagus after transthoracic and transhiatal esophagectomy. World J Surg Oncol. 2012;10:130.
Fujii H, Kitagawa Y, Kitajima M, Kubo A. Sentinel nodes of malignancies originating in the alimentary tract. Ann Nucl Med. 2004;18:1–12.
Kitagawa Y, Ohgami M, Fujii H, Mukai M, Kubota T, Ando N, et al. Laparoscopic detection of sentinel lymph nodes in gastrointestinal cancer: a novel and minimally invasive approach. Ann Surg Oncol. 2001;8:86S–9S.
Bohanes T, Neoral C, Aujesky R, Vrba R, Klein J, Koranda P. Sentinel lymph node in esophageal cancer before neoadjuvant therapy. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2005;149:145–7.
Burian M, Stein HJ, Sendler A, Piert M, Nahrig J, Feith M, et al. Sentinel node detection in Barrett’s and cardia cancer. Ann Surg Oncol. 2004;11:255S–8S.
Lamb PJ, Griffin SM, Burt AD, Lloyd J, Karat D, Hayes N. Sentinel node biopsy to evaluate the metastatic dissemination of oesophageal adenocarcinoma. Br J Surg. 2005;92:60–7.
Filip B, Scarpa M, Cavallin F, Alfieri R, Cagol M, Castoro C. Minimally invasive surgery for esophageal cancer: a review on sentinel node concept. Surg Endosc. 2014;28:1238–49.
Kitagawa Y, Kitajima M. Gastrointestinal cancer and sentinel node navigation surgery. J Surg Oncol. 2002;79:188–93.
Kitagawa Y, Fujii H, Mukai M, Kubota T, Ando N, Ozawa S, et al. Intraoperative lymphatic mapping and sentinel lymph node sampling in esophageal and gastric cancer. Surg Oncol Clin N Am. 2002;11:293–304.
Aikou T, Kitagawa Y, Kitajima M, Uenosono Y, Bilchik AJ, Martinez SR, et al. Sentinel lymph node mapping with GI cancer. Cancer Metastasis Rev. 2006;25:269–77.
Suga K, Shimizu K, Kawakami Y, Tangoku A, Zaki M, Matsunaga N, et al. Lymphatic drainage from esophagogastric tract: feasibility of endoscopic CT lymphography for direct visualization of pathways. Radiology. 2005;237:952–60.
Hayashi H, Tangoku A, Suga K, Shimizu K, Ueda K, Yoshino S, et al. CT lymphography-navigated sentinel lymph node biopsy in patients with superficial esophageal cancer. Surgery. 2006;139:224–35.
Suga K, Yuan Y, Okada M, Matsunaga N, Tangoku A, Yamamoto S, et al. Breast sentinel lymph node mapping at CT lymphography with iopamidol: preliminary experience. Radiology. 2004;230:543–52.
Suga K, Yuan Y, Ueda K, Kaneda Y, Kawakami Y, Zaki M, et al. Computed tomography lymphography with intrapulmonary injection of iopamidol for sentinel lymph node localization. Invest Radiol. 2004;39:313–24.
Tangoku A, Yamamoto S, Suga K, Ueda K, Nagashima Y, Hida M, et al. Sentinel lymph node biopsy using computed tomography-lymphography in patients with breast cancer. Surgery. 2004;135:258–65.
Imano H, Motoyama S, Saito R, Minamiya Y, Katayose Y, Okuyama M, et al. Superior mediastinal and neck lymphatic mapping in mid- and lower-thoracic esophageal cancer as defined by ferumoxides-enhanced magnetic resonance imaging. Jpn J Thorac Cardiovasc Surg. 2004;52:445–50.
Motoyama S, Ishiyama K, Maruyama K, Okuyama M, Sato Y, Hayashi K, et al. Preoperative mapping of lymphatic drainage from the tumor using ferumoxide-enhanced magnetic resonance imaging in clinical submucosal thoracic squamous cell esophageal cancer. Surgery. 2007;141:736–47.
Ishiyama K, Motoyama S, Tomura N, Sashi R, Imano H, Ogawa J, et al. Visualization of lymphatic basin from the tumor using magnetic resonance lymphography with superparamagnetic iron oxide in patients with thoracic esophageal cancer. J Comput Assist Tomogr. 2006;30:270–5.
Nishimura H, Tanigawa N, Hiramatsu M, Tatsumi Y, Matsuki M, Narabayashi I. Preoperative esophageal cancer staging: magnetic resonance imaging of lymph node with ferumoxtran-10, an ultrasmall superparamagnetic iron oxide. J Am Coll Surg. 2006;202:604–11.
The authors declare that they have no competing interests.
JB, MGGH, MEIS, FPV, IHMBR, RJDH, JPR, and RVH contributed to the conception and design. JB and RJDH provided administrative support. IHMBR, JPR, and RVH were responsible for provision of study materials or patients. JB, MGGH, MEIS, RJDH, and RVH were responsible for collection and assembly of data. JB, MGGH, MEIS, RJDH, JPR, and RVH were involved in data analysis and interpretation. Manuscript writing was done by JB, MGGH, MEIS, FPV, IHMBR, RJDH, JPR, and RVH. Final approval of manuscript was done by JB, MGGH, MEIS, FPV, IHMBR, RJDH, JPR and RVH.
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Boone, J., Hobbelink, M.G.G., Schipper, M.E.I. et al. Sentinel node biopsy during thoracolaparoscopic esophagectomy for advanced esophageal cancer. World J Surg Onc 14, 117 (2016). https://doi.org/10.1186/s12957-016-0866-9
- Esophageal cancer
- Sentinel lymph node biopsy
- Lymphatic metastasis
- Minimally invasive surgery