Precise Pathologic Examination Decreases the False-Negative Rate of Sentinel Lymph Node Biopsy in Gastric Cancer View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-10-07

AUTHORS

Hye Seung Lee, Hee Eun Lee, Do Joong Park, Young Soo Park, Hyung-Ho Kim

ABSTRACT

BackgroundGastric cancer has been identified as a target for sentinel lymph node (SLN) navigational surgery. Although accurate evaluation of SLNs is essential for applying the SLN concept to gastric cancer surgery, there is no standardized pathologic examination protocol for SLNs in gastric cancer.MethodsA total of 231 SLNs from 69 patients with cT1–2, N0 gastric cancer were prospectively examined in this study. During the operation, SLNs were sliced at 2-mm intervals, and frozen sections were analyzed by hematoxylin and eosin (HE) staining in 35 patients or HE staining with rapid immunohistochemistry (IHC) for pancytokeratin (CK) in 34 patients. HE staining and CK IHC were performed postoperatively on each remaining SLN. Non-SLNs were evaluated with 2 levels of HE slides and 1 CK IHC.ResultsOf 35 patients, metastasis was identified in 10 patients by intraoperative HE staining, and in 12 patients by postoperative HE staining and CK IHC. Two patients had isolated tumor cells (ITCs) detectable by postoperative CK IHC; these patients had non-SLN metastasis. We enrolled another 34 patients and examined 147 SLNs by frozen HE and rapid IHC. In this cohort, 26 patients with negative SLNs by intraoperative examination did not have non-SLN metastasis even after deeper sectioning and CK IHC of non-SLNs (sensitivity, 100%; false negative value, 0%).ConclusionsOur study indicated that precise and detailed intraoperative examination decreases the false-negative rate of SLN biopsy. ITCs in SLNs should not be overlooked, and rapid IHC can be helpful for detecting ITCs intraoperatively. More... »

PAGES

772-778

Identifiers

URI

http://scigraph.springernature.com/pub.10.1245/s10434-011-2106-4

DOI

http://dx.doi.org/10.1245/s10434-011-2106-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1020425501

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21979113


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