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Analysis of Histologic Features Suspecting Anaplastic Lymphoma Kinase (ALK)-Expressing Pulmonary Adenocarcinoma

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dc.contributor.authorChoi, In Ho-
dc.contributor.authorKim, Dong Won-
dc.contributor.authorHa, Sang Yun-
dc.contributor.authorChoi, Yoon-La-
dc.contributor.authorLee, Hee Jeong-
dc.contributor.authorHan, Joungho-
dc.date.accessioned2021-08-11T19:46:57Z-
dc.date.available2021-08-11T19:46:57Z-
dc.date.issued2015-07-
dc.identifier.issn2383-7837-
dc.identifier.issn2383-7845-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/10526-
dc.description.abstractBackground: Since 2007 when anaplastic lymphoma kinase (ALK) rearrangements were discovered in non-small cell lung cancer, the ALK gene has received attention due to ALK-targeted therapy, and a notable treatment advantage has been observed in patients harboring the EML4/ALK translocation. However, using ALK-fluorescence in situ hybridization (FISH) as the standard method has demerits such as high cost, a time-consuming process, dependency on interpretation skill, and tissue preparation. We analyzed the histologic findings which could complement the limitation of ALK-FISH test for pulmonary adenocarcinoma. Methods: Two hundred five cases of ALK-positive and 101 of ALK-negative pulmonary adenocarcinoma from January 2007 to May 2013 were enrolled in this study. The histologic findings and ALK immunohistochemistry results were reviewed and compared with the results of ALK-FISH and EGFR/KRAS mutation status. Results: Acinar, cribriform, and solid growth patterns, extracellular and intracellular mucin production, and presence of signet-ring-cell element, and psammoma body were significantly more often present in ALK-positive cancer. In addition, the presence of goblet cell-like cells and presence of nuclear inclusion and groove resembling papillary thyroid carcinoma were common in the ALK-positive group. Conclusions: The above histologic parameters can be helpful in predicting ALK rearranged pulmonary adenocarcinoma, leading to rapid FISH analysis and timely treatment.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisher대한병리학회-
dc.titleAnalysis of Histologic Features Suspecting Anaplastic Lymphoma Kinase (ALK)-Expressing Pulmonary Adenocarcinoma-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4132/jptm.2015.05.13-
dc.identifier.scopusid2-s2.0-84942941495-
dc.identifier.wosid000218425500004-
dc.identifier.bibliographicCitationJournal of Pathology and Translational Medicine, v.49, no.4, pp 310 - 317-
dc.citation.titleJournal of Pathology and Translational Medicine-
dc.citation.volume49-
dc.citation.number4-
dc.citation.startPage310-
dc.citation.endPage317-
dc.type.docTypeArticle-
dc.identifier.kciidART002013163-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaPathology-
dc.relation.journalWebOfScienceCategoryPathology-
dc.subject.keywordAuthorLung-
dc.subject.keywordAuthorAdenocarcinoma-
dc.subject.keywordAuthorAnaplastic large cell lymphoma kinase-
dc.subject.keywordAuthorAnaplastic lymphoma kinase-
dc.subject.keywordAuthorIn situ hybridization-
dc.subject.keywordAuthorfluorescence-
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