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一名有乳腺囊内乳头状癌病史的患者发生多形性肺癌且GATA3呈阳性的罕见病例:原发性肺癌还是转移性疾病?

A Rare Case of GATA3 Positivity in Pleomorphic Lung Carcinoma in a Patient with History of Intracystic Papillary Carcinoma of the Breast: Primary Lung or Metastatic Disease?

作者信息

Abada Evi

机构信息

Department of Pathology, Wayne State University School of Medicine, 4707 St. Antoine Blvd. Detroit, Michigan 48201, USA.

出版信息

Case Rep Pathol. 2021 Jan 20;2021:6664804. doi: 10.1155/2021/6664804. eCollection 2021.

Abstract

Pleomorphic lung carcinoma is a rare and aggressive neoplasm accounting for <1% of all lung tumors. It is more common in men and consists of spindle and/or giant cells with an epithelial component. In patients with known histories of malignancies at other sites, diagnosis of a new lung lesion may prove challenging with respect to classification as either primary or metastatic disease, especially in cases with overlapping immunohistochemical staining patterns. This was a case of a 67-year-old female with a newly discovered 1.5 cm nodule in her left lower lung lobe. Her past medical history was significant for an intracystic papillary carcinoma of the right breast diagnosed 8 years prior. Histopathologic examination of the new lung lesion revealed highly pleomorphic cells composed predominantly of neoplastic giant cells and atypical mitotic figures, with geographic areas of necrosis. However, no areas reminiscent of intracystic papillary carcinoma or other forms of breast carcinoma were seen. Immunohistochemistry showed that the tumor cells were immunoreactive for GATA3, TTF1, and napsin A and nonimmunoreactive for p40. Therefore, although this index lung tumor did show positivity with GATA3 staining, it was morphologically different from her original intracystic papillary carcinoma of the breast. In addition, intracystic papillary carcinomas are known to rarely metastasize to other organs, and GATA3 staining has been rarely reported in lung carcinomas. In summary, this case typifies the overlapping immunohistochemical staining patterns that may be seen in different tumors and the role of histopathologic morphology in arriving at the correct diagnosis.

摘要

多形性肺癌是一种罕见且侵袭性强的肿瘤,占所有肺部肿瘤的比例不到1%。它在男性中更为常见,由梭形和/或巨细胞以及上皮成分组成。对于有其他部位恶性肿瘤病史的患者,新发现的肺部病变在分类为原发性或转移性疾病方面可能具有挑战性,尤其是在免疫组化染色模式重叠的情况下。这是一例67岁女性患者,其左肺下叶新发现一个1.5厘米的结节。她的既往病史中有8年前诊断出的右乳腺囊内乳头状癌。对新肺部病变的组织病理学检查显示,细胞高度多形性,主要由肿瘤巨细胞和非典型有丝分裂象组成,并有大片坏死区域。然而,未见类似囊内乳头状癌或其他形式乳腺癌的区域。免疫组化显示肿瘤细胞对GATA3、TTF1和napsin A呈免疫反应,对p40无免疫反应。因此,尽管该肺部肿瘤在GATA3染色中呈阳性,但在形态上与她最初的乳腺囊内乳头状癌不同。此外,已知囊内乳头状癌很少转移至其他器官,且GATA3染色在肺癌中的报道也很少。总之,该病例体现了不同肿瘤中可能出现的重叠免疫组化染色模式以及组织病理学形态在做出正确诊断中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2b/7840265/d84d9a145d92/CRIPA2021-6664804.001.jpg

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