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首页> 外文期刊>Journal of vascular and interventional radiology: JVIR >Ultrasound-guided core biopsy of small renal masses: Diagnostic rate and limitations
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Ultrasound-guided core biopsy of small renal masses: Diagnostic rate and limitations

机译:小肾脏肿块的超声引导下核心活检:诊断率和局限性

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Purpose: To evaluate the feasibility and complications of ultrasound (US)-guided biopsy of small renal masses (SRMs) and to determine factors that contribute to nondiagnostic biopsy specimens. Materials and Methods: Between June 2004 and May 2011, 58 consecutive patients underwent US-guided core biopsy of a SRM (>1 cm and??4 cm) using an 18-gauge core biopsy device. The diagnostic rate, histologic diagnosis, and complications of US-guided core biopsy were assessed. Mann-Whitney U and Fisher exact tests were used to compare diagnostic and nondiagnostic biopsy specimens. Univariate analysis was performed to determine the predictive factors for nondiagnostic biopsy specimens. Results: There were 59 biopsies of SRMs performed, and the diagnostic rate was 81% (48 of 59). The mass size of diagnostic and nondiagnostic biopsy specimens ranged from 1.2-3.9 cm (2.4 cm??0.7) for diagnostic specimens and from 1.1-3.5 cm (1.9 cm??0.7) for nondiagnostic specimens (P=.024). Of the diagnostic biopsy specimens, 77% (37 of 48) were malignant, and 23% (11 of 48) were benign. Minor complications developed in 20.3% (12 of 59) of biopsies. The lesion size or core number threshold for decreasing diagnostic rate was 2 cm or three cores. A cystic mass, fewer cores (three or fewer cores), an upper pole mass, and a small mass (??2 cm) significantly predicted a nondiagnostic biopsy specimen (P=.007-.046). Conclusions: US-guided core biopsy is a feasible and safe procedure for histologic diagnosis of a SRM. However, nondiagnostic rates may increase when a cystic mass is biopsied, a mass is located in an upper pole mass, a mass is 2 cm or less, and three cores or fewer are sampled. ? 2013 SIR.
机译:目的:评估超声引导下小肾脏肿块(SRM)活检的可行性和并发症,并确定导致非诊断性活检标本的因素。材料和方法:2004年6月至2011年5月之间,连续有58例患者使用18口径核心活检设备接受了美国指导的SRM(> 1 cm和?4 cm)活检。评估了美国引导的核心活检的诊断率,组织学诊断和并发症。使用Mann-Whitney U和Fisher精确测试来比较诊断性和非诊断性活检标本。进行单因素分析以确定非诊断性活检标本的预测因素。结果:共进行了59例SRM活检,诊断率为81%(59中的48)。诊断性和非诊断性活检标本的质量范围为诊断性标本为1.2-3.9厘米(2.4 cm -0.7),非诊断性标本为1.1-3.5厘米(1.9 cm -0.7)(P = .024)。在诊断性活检标本中,有77%(48个中的37个)是恶性的,而23%(48个中的11个)是良性的。 20.3%(59例中的12例)活检有轻微并发症。降低诊断率的病变大小或核心数阈值为2 cm或三个核心。囊性肿块,更少的核(三个或更少的核),上极块和小的肿块(?2 cm)显着预测了不可诊断的活检标本(P = .007-.046)。结论:美国引导的核心活检是一种可行且安全的SRM组织学诊断方法。但是,当对囊性肿块进行活检,肿块位于上极肿块中,肿块为2 cm或更小并且取样的芯数为三个或更少时,非诊断率可能会增加。 ? 2013年SIR。

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