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超声造影(CEUS)在犬猫非心脏性胸部疾病诊断中的可行性。

The feasibility of contrast enhanced ultrasonography (CEUS) in the diagnosis of non-cardiac thoracic disorders of dogs and cats.

作者信息

Linta N, Baron Toaldo M, Bettini G, Cordella A, Quinci M, Pey P, Galli V, Cipone M, Diana A

机构信息

Department of Veterinary Medical Sciences, Alma Mater Studiorum - University of Bologna, Via Tolara di Sopra 50, I-40064, Ozzano Emilia, Bologna, Italy.

ANTECH Imaging Services, 17672-B Cowan Avenue, Irvine, CA, 92614, USA.

出版信息

BMC Vet Res. 2017 May 25;13(1):141. doi: 10.1186/s12917-017-1061-0.

DOI:10.1186/s12917-017-1061-0
PMID:28545570
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5445396/
Abstract

BACKGROUND

This study describes the feasibility of Contrast Enhanced Ultrasonography (CEUS) in the diagnostic work-up of non-cardiac thoracic disorders of small animals. The second aim is to assess the usefulness of CEUS as a direct guide for sample procedures.

RESULTS

Forty animals, 28 dogs and 12 cats, were included in the study. Thoracic disorders included 23 pulmonary lesions [primary carcinoma (14), lymphoma (1), sarcoma (1), histiocytic sarcoma (1), abscess (1) and pneumonia (5)] and 17 mediastinal lesions [lymphoma (8), thymoma (3), mesothelioma (1), melanoma (1), carcinomatous lymphadenopathy (1), mixsosarcoma (1), lipoma (1), and abscess (1)]. The majority of neoplastic pulmonary lesions showed an inhomogeneous distribution of contrast medium, whereas inflammatory lesions had a homogenous distribution with typical pulmonary vessels ramification. The majority of mediastinal malignant lesions showed an inhomogeneous distribution pattern. The lung and mediastinal abscesses had peripheral enhancement of the wall with an avascular center. All cytological and biopsy samples obtained after CEUS were diagnostic. Quantitative analysis, performed in 19/23 pulmonary lesions, showed a statistically significant difference (P < 0.0001) between the arrival time of the malignant (7.27 s - range 4.46-13.52 s) and benign (4.52 s - range 2.87-6.06 s) pulmonary lesions.

CONCLUSIONS

CEUS may be a useful tool for the evaluation of non-cardiac thoracic lesions. The contrast medium allows for the precise definition of lesion edges, the presence of necrotic areas, and the distribution of pulmonary vessels. Based on our preliminary results, the use of ultrasonographic contrast medium can be recommended for improving the diagnostic usefulness of cytology and biopsy sampling, because CEUS may help to define necrotic areas from viable tissue.

摘要

背景

本研究描述了对比增强超声(CEUS)在小动物非心脏性胸部疾病诊断检查中的可行性。第二个目的是评估CEUS作为样本采集程序直接引导手段的效用。

结果

本研究纳入了40只动物,其中28只狗和12只猫。胸部疾病包括23例肺部病变[原发性癌(14例)、淋巴瘤(1例)、肉瘤(1例)、组织细胞肉瘤(1例)、脓肿(1例)和肺炎(5例)]以及17例纵隔病变[淋巴瘤(8例)、胸腺瘤(3例)、间皮瘤(1例)、黑色素瘤(1例)、癌性淋巴结病(1例)、混合肉瘤(1例)、脂肪瘤(1例)和脓肿(1例)]。大多数肺部肿瘤性病变显示造影剂分布不均匀,而炎症性病变造影剂分布均匀,有典型的肺血管分支。大多数纵隔恶性病变显示不均匀的分布模式。肺部和纵隔脓肿壁的周边有强化,中心无血管。CEUS后获取的所有细胞学和活检样本均具有诊断价值。对19/23例肺部病变进行的定量分析显示,恶性(7.27秒 - 范围4.46 - 13.52秒)和良性(4.52秒 - 范围2.87 - 6.06秒)肺部病变的造影剂到达时间存在统计学显著差异(P < 0.0001)。

结论

CEUS可能是评估非心脏性胸部病变的有用工具。造影剂有助于精确界定病变边缘、坏死区域的存在以及肺血管的分布。基于我们的初步结果,推荐使用超声造影剂以提高细胞学和活检采样的诊断效用,因为CEUS可能有助于区分坏死组织和存活组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/a4bb9ed4845c/12917_2017_1061_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/eba2aed08a82/12917_2017_1061_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/71b3f1f8b53f/12917_2017_1061_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/6eca3e9428fd/12917_2017_1061_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/f056d76fab8a/12917_2017_1061_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/02568bcd9f8e/12917_2017_1061_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/a4bb9ed4845c/12917_2017_1061_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/eba2aed08a82/12917_2017_1061_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/71b3f1f8b53f/12917_2017_1061_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/6eca3e9428fd/12917_2017_1061_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/f056d76fab8a/12917_2017_1061_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/02568bcd9f8e/12917_2017_1061_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ad/5445396/a4bb9ed4845c/12917_2017_1061_Fig6_HTML.jpg

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