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肺肉瘤样癌:一例罕见的合并三例小肠套叠病例及文献综述

Sarcomatoid Carcinoma of the lung: A rare case of three small intestinal intussusceptions and literature review.

作者信息

Romano Angela, Grassia Michele, Rossetti Amalia Rosaria Rita, Esposito Giuseppe, Braccio Bartolomeo, Pezzella Modestino, Torelli Francesco, Izzo Giuseppe, Alfano Roberto, Martino Natale Di

机构信息

Department of General Surgery, Second University of Naples, Italy.

出版信息

Int J Surg Case Rep. 2015;13:48-50. doi: 10.1016/j.ijscr.2015.05.025. Epub 2015 Jun 10.

Abstract

INTRODUCTION

Sarcomatoid carcinoma is an extremely rare, biphasic tumor characterized by a combination of malignant epithelial and mesenchymal cells. Limited data showed that most cases occurred with advanced local disease and metastasis.

PRESENTATION OF CASE

We present a rare case of a 60-year-old man with three small intestinal intussusceptions due to metastatic pulmonary carcinosarcoma. He was explored for chest pain and hemoptysis in Emergency room. Due to his chest symptoms he had a computed tomography (CT) scan of the chest which showed a lesion about 60mm in diameter in the inferior lobe of the left lung. After 2 weeks physical examination demonstrated a distended abdomen and auscultation was indicated by hyperactive bowel sounds. Further imaging studies with abdominal computed tomography (CT) scan, showed multiple protruding small bowel tumors with entero enteric intussusceptions at three sites requiring a massive bowel resection at surgery. The pathology showed that it was positive for cytokeratin, vimentin, CD-34, and LIS; CK7 was focally positive; and CD117, CD20, and desmine were negative. The final diagnosis was metastatic small bowel carcinosarcoma with a lung primary.

DISCUSSION

Lung carcinosarcoma is a high grade biphase neoplasm. The survival rate at 6 months is only around 27%.

CONCLUSION

There are rare reports of small intestinal intussusceptions caused by metastatic lung carcinosarcoma, this presentation shows the third case in literature. Physicians should be more alert to symptoms or signs indicating GI metastais in patients with a history of lung cancer.

摘要

引言

肉瘤样癌是一种极其罕见的双相性肿瘤,其特征为恶性上皮细胞和间充质细胞的组合。有限的数据显示,大多数病例发生时伴有局部晚期疾病和转移。

病例介绍

我们报告一例罕见病例,一名60岁男性因转移性肺肉瘤样癌出现三处小肠套叠。他因胸痛和咯血在急诊室接受检查。由于其胸部症状,他进行了胸部计算机断层扫描(CT),显示左肺下叶有一个直径约60mm的病变。2周后体格检查发现腹部膨隆,听诊提示肠鸣音亢进。进一步的腹部计算机断层扫描(CT)成像研究显示,多处小肠肿瘤突出,在三个部位出现肠-肠套叠,手术时需要进行大范围肠切除。病理检查显示细胞角蛋白、波形蛋白、CD-34和LIS呈阳性;CK7局灶性阳性;CD117、CD20和平滑肌肌动蛋白呈阴性。最终诊断为原发性肺癌伴转移性小肠肉瘤样癌。

讨论

肺肉瘤样癌是一种高级别双相性肿瘤。6个月时的生存率仅约为27%。

结论

转移性肺肉瘤样癌导致小肠套叠的报道罕见,本病例是文献中的第三例。医生应对有肺癌病史的患者出现的提示胃肠道转移的症状或体征更加警惕。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/756a/4529630/ae173106ab3f/gr1.jpg

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