Diagnostic ability of a 22G Franseen needle in endoscopic ultrasound-guided fine needle aspiration of subepithelial lesions
The differential diagnosis of gastrointestinal subepithelial lesions (SELs) such as gastrointestinal stromal tumors from other benign tumors is important. In the present study, adequate sample rates of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) with a 22G Franseen needle for SELs...
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| Veröffentlicht in: | Molecular and clinical oncology 2018-11, Vol.9 (5), p.527-531 |
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| creator | Fujita, Akashi Ryozawa, Shomei Kobayashi, Masanori Araki, Ryuichiro Nagata, Koji Minami, Kazuhiro Tanisaka, Yuki Kobatake, Tsutomu Mizuide, Masafumi |
| description | The differential diagnosis of gastrointestinal subepithelial lesions (SELs) such as gastrointestinal stromal tumors from other benign tumors is important. In the present study, adequate sample rates of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) with a 22G Franseen needle for SELs were evaluated. The present study included 57 consecutive lesions (61 sessions) of EUS-FNA using a 22G needle to evaluate SELs between July 2013 and October 2017. Adequate sample rates were compared retrospectively between a 22G conventional needle group (C group) and a 22G Franseen needle group (F group). The overall adequate sample rate was 80.3%. The adequate sample rates in the C and F groups were 75.0% (33/44) and 94.1% (16/17), respectively (P=0.15). For lesions ≥20 mm, the adequate sample rates were 82.8% (24/29) in the C group and 91.7% (11/12) in the F group, 8.9% higher in the F group. However, for lesions |
| doi_str_mv | 10.3892/mco.2018.1709 |
| format | Article |
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In the present study, adequate sample rates of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) with a 22G Franseen needle for SELs were evaluated. The present study included 57 consecutive lesions (61 sessions) of EUS-FNA using a 22G needle to evaluate SELs between July 2013 and October 2017. Adequate sample rates were compared retrospectively between a 22G conventional needle group (C group) and a 22G Franseen needle group (F group). The overall adequate sample rate was 80.3%. The adequate sample rates in the C and F groups were 75.0% (33/44) and 94.1% (16/17), respectively (P=0.15). For lesions ≥20 mm, the adequate sample rates were 82.8% (24/29) in the C group and 91.7% (11/12) in the F group, 8.9% higher in the F group. However, for lesions <20 mm, the adequate sample rates were 60% (9/15) in the C group and 100% (5/5) in the F group, 40% higher in the F group (P=0.65, 0.26). In conclusion, the results of the present study suggested that using a 22G Franseen needle for EUS-FNA evaluation of SELs may improve adequate sample rates in small lesions <20 mm in diameter.</description><identifier>ISSN: 2049-9450</identifier><identifier>EISSN: 2049-9469</identifier><identifier>DOI: 10.3892/mco.2018.1709</identifier><identifier>PMID: 30345047</identifier><language>eng</language><publisher>England: Spandidos Publications UK Ltd</publisher><subject>Accuracy ; Endoscopy ; Esophagus ; Gastrointestinal cancer ; Histopathology ; Medical diagnosis ; Oncology ; Patients ; Tumors ; Ultrasonic imaging</subject><ispartof>Molecular and clinical oncology, 2018-11, Vol.9 (5), p.527-531</ispartof><rights>Copyright Spandidos Publications UK Ltd. 2018</rights><rights>Copyright © 2018, Spandidos Publications 2018</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-fe216ba829f34d3657f249a6f2f2f3df72983e5e9fa98157c3e55f9fcee17353</citedby><cites>FETCH-LOGICAL-c411t-fe216ba829f34d3657f249a6f2f2f3df72983e5e9fa98157c3e55f9fcee17353</cites><orcidid>0000-0001-9475-0512 ; 0000-0003-4128-9990</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174453/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174453/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30345047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujita, Akashi</creatorcontrib><creatorcontrib>Ryozawa, Shomei</creatorcontrib><creatorcontrib>Kobayashi, Masanori</creatorcontrib><creatorcontrib>Araki, Ryuichiro</creatorcontrib><creatorcontrib>Nagata, Koji</creatorcontrib><creatorcontrib>Minami, Kazuhiro</creatorcontrib><creatorcontrib>Tanisaka, Yuki</creatorcontrib><creatorcontrib>Kobatake, Tsutomu</creatorcontrib><creatorcontrib>Mizuide, Masafumi</creatorcontrib><title>Diagnostic ability of a 22G Franseen needle in endoscopic ultrasound-guided fine needle aspiration of subepithelial lesions</title><title>Molecular and clinical oncology</title><addtitle>Mol Clin Oncol</addtitle><description>The differential diagnosis of gastrointestinal subepithelial lesions (SELs) such as gastrointestinal stromal tumors from other benign tumors is important. In the present study, adequate sample rates of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) with a 22G Franseen needle for SELs were evaluated. The present study included 57 consecutive lesions (61 sessions) of EUS-FNA using a 22G needle to evaluate SELs between July 2013 and October 2017. Adequate sample rates were compared retrospectively between a 22G conventional needle group (C group) and a 22G Franseen needle group (F group). The overall adequate sample rate was 80.3%. The adequate sample rates in the C and F groups were 75.0% (33/44) and 94.1% (16/17), respectively (P=0.15). For lesions ≥20 mm, the adequate sample rates were 82.8% (24/29) in the C group and 91.7% (11/12) in the F group, 8.9% higher in the F group. However, for lesions <20 mm, the adequate sample rates were 60% (9/15) in the C group and 100% (5/5) in the F group, 40% higher in the F group (P=0.65, 0.26). In conclusion, the results of the present study suggested that using a 22G Franseen needle for EUS-FNA evaluation of SELs may improve adequate sample rates in small lesions <20 mm in diameter.</description><subject>Accuracy</subject><subject>Endoscopy</subject><subject>Esophagus</subject><subject>Gastrointestinal cancer</subject><subject>Histopathology</subject><subject>Medical diagnosis</subject><subject>Oncology</subject><subject>Patients</subject><subject>Tumors</subject><subject>Ultrasonic imaging</subject><issn>2049-9450</issn><issn>2049-9469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkc1LHTEUxUOxqFiXbkugm27mmY9JZrIRitYPENy4D3mZm2ckLxmTmYL4z5up-mjNXSS598fhXA5CJ5SseK_Y6damFSO0X9GOqC_okJFWNaqVam_3FuQAHZfySOpRHWFC7aMDTngdtN0hernwZhNTmbzFZu2Dn55xcthgxq7wZTaxAEQcAYYA2EcMcUjFprHic5iyKWmOQ7OZ_QADdj7CB2vK6LOZfIqLXpnXMPrpAYI3AQcotV--oa_OhALH7_cRur_8fX9-3dzeXd2c_7ptbEvp1DhgVK5Nz5Tj7cCl6BxrlZGO1eKD65jqOQhQzqieis7Wj3DKWQDaccGP0Nmb7DivtzBYiNV30GP2W5OfdTJe_z-J_kFv0h8tade2gleBn-8COT3NUCa99cVCCCZCmotmlAmmZM9kRX98Qh_TnGPd7i9FJZdqcdS8UTanUjK4nRlK9BKsrsHqJVi9BFv57_9usKM_YuSvFYeg3A</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Fujita, Akashi</creator><creator>Ryozawa, Shomei</creator><creator>Kobayashi, Masanori</creator><creator>Araki, Ryuichiro</creator><creator>Nagata, Koji</creator><creator>Minami, Kazuhiro</creator><creator>Tanisaka, Yuki</creator><creator>Kobatake, Tsutomu</creator><creator>Mizuide, Masafumi</creator><general>Spandidos Publications UK Ltd</general><general>D.A. 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In the present study, adequate sample rates of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) with a 22G Franseen needle for SELs were evaluated. The present study included 57 consecutive lesions (61 sessions) of EUS-FNA using a 22G needle to evaluate SELs between July 2013 and October 2017. Adequate sample rates were compared retrospectively between a 22G conventional needle group (C group) and a 22G Franseen needle group (F group). The overall adequate sample rate was 80.3%. The adequate sample rates in the C and F groups were 75.0% (33/44) and 94.1% (16/17), respectively (P=0.15). For lesions ≥20 mm, the adequate sample rates were 82.8% (24/29) in the C group and 91.7% (11/12) in the F group, 8.9% higher in the F group. However, for lesions <20 mm, the adequate sample rates were 60% (9/15) in the C group and 100% (5/5) in the F group, 40% higher in the F group (P=0.65, 0.26). In conclusion, the results of the present study suggested that using a 22G Franseen needle for EUS-FNA evaluation of SELs may improve adequate sample rates in small lesions <20 mm in diameter.</abstract><cop>England</cop><pub>Spandidos Publications UK Ltd</pub><pmid>30345047</pmid><doi>10.3892/mco.2018.1709</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-9475-0512</orcidid><orcidid>https://orcid.org/0000-0003-4128-9990</orcidid><oa>free_for_read</oa></addata></record> |
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| subjects | Accuracy Endoscopy Esophagus Gastrointestinal cancer Histopathology Medical diagnosis Oncology Patients Tumors Ultrasonic imaging |
| title | Diagnostic ability of a 22G Franseen needle in endoscopic ultrasound-guided fine needle aspiration of subepithelial lesions |
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