Ultrasound-guided vs endoscopic ultrasound-guided fine-needle aspiration for pancreatic cancer diagnosis

被引:15
作者
Matsuyama, Masato [1 ]
Ishii, Hiroshi [1 ]
Kuraoka, Kensuke [1 ]
Yukisawa, Seigo [1 ]
Kasuga, Akiyoshi [1 ]
Ozaka, Masato [1 ]
Suzuki, Sho [1 ]
Takano, Kouichi [1 ]
Sugiyama, Yuko [2 ]
Itoi, Takao [3 ]
机构
[1] Canc Inst Hosp, Dept Gastroenterol, Tokyo 1358550, Japan
[2] Canc Inst Hosp, Dept Gynecol, Tokyo 1358550, Japan
[3] Tokyo Med Univ, Dept Gastroenterol & Hepatol, Tokyo 1600023, Japan
关键词
Endoscopic ultrasound-guided fine needle aspiration; Percutaneous needle aspiration; Pancreatic cancer; SINGLE-CENTER EXPERIENCE; 19-GAUGE TRUCUT NEEDLE; EUS-FNA; BIOPSY; ULTRASONOGRAPHY; MASSES; TUMOR; COMPLICATIONS; CARCINOMA; CYTOLOGY;
D O I
10.3748/wjg.v19.i15.2368
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To clarify the effectiveness and safety of endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) for the diagnosis of pancreatic cancer (PC). METHODS: Patients who were diagnosed with unresectable, locally advanced or metastatic PC between February 2006 and September 2011 were selected for this retrospective study. FNA biopsy for pancreatic tumors had been performed percutaneously under extracorporeal ultrasound guidance until October 2009; then, beginning in November 2009, EUS-FNA has been performed. We reviewed the complete medical records of all patients who met the selection criteria for the following data: sex, age, location and size of the targeted tumor, histological and/or cytological findings, details of puncture procedures, time from day of puncture until day of definitive diagnosis, and details of severe adverse events. RESULTS: Of the 121 patients who met the selection criteria, 46 had a percutaneous biopsy (Group A) and 75 had an EUS-FNA biopsy (Group B). Adequate cytological specimens were obtained in 42 Group A patients (91.3%) and all 75 Group B patients (P = 0.0192), and histological specimens were obtained in 41 Group A patients (89.1%) and 65 Group B patients (86.7%). Diagnosis of malignancy by cytology was positive in 33 Group A patients (78.6%) and 72 Group B patients (94.6%) (P = 0.0079). Malignancy by both cytology and pathology was found in 43 Group A (93.5%) and 73 Group B (97.3%) patients. The mean period from the puncture until the cytological diagnosis in Group B was 1.7 d, which was significantly shorter than that in Group A (4.1 d) (P < 0.0001). Severe adverse events were experienced in two Group A patients (4.3%) and in one Group B patient (1.3%). CONCLUSION: EUS-FNA, as well as percutaneous needle aspiration, is an effective modality to obtain cytopathological confirmation in patients with advanced PC. (C) 2013 Baishideng. All rights reserved.
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收藏
页码:2368 / 2373
页数:6
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