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IA 期原发性肺高分化黏液表皮样癌伴囊性气腔快速转移:1 例报告及反思。

Rapid metastasis of stage IA primary pulmonary high-grade mucoepidermoid carcinoma with a cystic airspace: a case report and reflection.

机构信息

Department of Operating Room, Lishui Hospital of Zhejiang University, Lishui Municipal Central Hospital, Lishui, Zhejiang Province, P.R. China.

Department of Cardiothoracic Surgery, Lishui Hospital of Zhejiang University, Lishui Municipal Central Hospital, Lishui, Zhejiang Province, P.R. China.

出版信息

J Int Med Res. 2021 Sep;49(9):3000605211038137. doi: 10.1177/03000605211038137.

Abstract

Primary pulmonary high-grade mucoepidermoid carcinoma (MEC) with a cystic airspace is uncommon, and early metastasis is extremely rare. In such cases, however, it is clinically important for clinicians to consider whether the tumor has spread to the lymph nodes through the cystic airspace. A 77-year-old man presented to our hospital with cough and hemoptysis. Chest computed tomography showed a 25-mm-diameter mass with a cystic airspace located in the upper lobe of the left lung. The possibility of malignancy was considered. Without a definitive preoperative diagnosis, left upper lobectomy and mediastinal lymphadenectomy were performed. Histopathological examination revealed the typical histological characteristics of high-grade MEC (stage IA) and no lymph node metastasis. However, lymph node metastasis was found 6 months after surgical resection, and radiochemotherapy was performed. The patient developed widespread metastatic disease 4 months following completion of radiochemotherapy and died 2 months later. Primary pulmonary MEC with a cystic airspace is a rare malignant disease with uncommon imaging findings. Complete surgical resection is the main treatment method for high-grade MEC. In this case, we hypothesize that early metastasis was caused by seeding of tumor cells through the cystic airspace.

摘要

原发性肺高级别黏液表皮样癌(MEC)伴囊性气腔并不常见,早期转移极为罕见。然而,在这种情况下,临床医生通过囊性气腔考虑肿瘤是否已经扩散到淋巴结,这对临床医生来说非常重要。一名 77 岁男性因咳嗽和咯血就诊于我院。胸部 CT 显示左肺上叶直径 25mm 的肿块伴囊性气腔。考虑为恶性肿瘤。由于术前没有明确诊断,行左肺上叶切除术和纵隔淋巴结清扫术。组织病理学检查显示高级别 MEC(IA 期)的典型组织学特征,且无淋巴结转移。然而,术后 6 个月发现淋巴结转移,行放化疗。放化疗完成后 4 个月患者出现广泛转移疾病,2 个月后死亡。原发性肺 MEC 伴囊性气腔是一种罕见的恶性疾病,影像学表现不常见。完全手术切除是高级别 MEC 的主要治疗方法。在本例中,我们假设早期转移是由于肿瘤细胞通过囊性气腔播种引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f121/8424610/3010bbccf5fc/10.1177_03000605211038137-fig1.jpg

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