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靶向测序有助于肺肿瘤的鉴别诊断:病例系列研究

Targeted sequencing may facilitate differential diagnostics of pulmonary tumours: a case series.

作者信息

Ericson-Lindquist Kajsa, Johansson Anna, Levéen Per, Elmberger Göran, Jönsson Göran, Staaf Johan, Brunnström Hans

机构信息

Department of Pathology, Regional Laboratories Region Skåne, SE-221 85, Lund, Sweden.

Department of Pathology, Örebro University Hospital, SE-701 85, Örebro, Sweden.

出版信息

Diagn Pathol. 2017 Mar 27;12(1):31. doi: 10.1186/s13000-017-0621-8.

Abstract

BACKGROUND

Histopathological diagnosis is important for prognostication and choice of treatment in patients with cancer in the lung. Metastases to the lungs are common and need to be distinguished from primary lung cancer. Furthermore, cases with synchronous or metachronous primary lung cancers (although infrequent) are often handled differently than cases with lung cancer with intrapulmonary metastasis or relapse, respectively. In some cases, morphology and immunohistochemical staining is not sufficient for certain diagnosis.

METHODS

The present study included six cases where molecular genetic analysis in form of pyrosequencing or targeted next-generation sequencing was of value for certain diagnosis of selected tumours in the lung.

RESULTS

Two of the included cases were rare metastases to the lung; colorectal cancer with IHC profile consistent with primary lung cancer and malignant adenomyoepithelioma of the breast, respectively, where molecular genetic analysis was of aid for proving the relationship to the primary tumour. The other four cases were multiple lung adenocarcinomas where molecular genetic analysis was of aid to distinguish between intrapulmonary metastasis and synchronous tumour.

CONCLUSIONS

Comparison of molecular genetic profile may be an important tool for determination of relationship between tumours in some situations and should always be considered in unclear cases. Further studies on concordance and discordance of molecular genetic profiles between spatially or temporally different tumours with common origin may be helpful for improved diagnostics of pulmonary tumours.

摘要

背景

组织病理学诊断对于肺癌患者的预后评估和治疗选择至关重要。肺转移瘤很常见,需要与原发性肺癌相鉴别。此外,同时性或异时性原发性肺癌病例(尽管不常见)的处理方式通常与肺内转移或复发的肺癌病例有所不同。在某些情况下,形态学和免疫组化染色不足以做出明确诊断。

方法

本研究纳入了6例病例,其中焦磷酸测序或靶向二代测序形式的分子遗传学分析对某些肺部肿瘤的明确诊断具有价值。

结果

纳入的病例中有2例是罕见的肺转移瘤,分别是免疫组化特征与原发性肺癌一致的结直肠癌和乳腺恶性腺肌上皮瘤,分子遗传学分析有助于证实与原发肿瘤的关系。另外4例是多发性肺腺癌,分子遗传学分析有助于区分肺内转移和同时性肿瘤。

结论

在某些情况下,分子遗传学特征的比较可能是确定肿瘤之间关系的重要工具,在不明确的病例中应始终予以考虑。对具有共同起源的空间或时间上不同肿瘤之间分子遗传学特征的一致性和不一致性进行进一步研究,可能有助于改善肺部肿瘤的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7542/5368924/eb075e4aee15/13000_2017_621_Fig1_HTML.jpg

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