Chen Dong, Zhu Guangfa, Wang Dijia, Zhang Zhe, Fang Wei, Qu Zheng
Department of Pathology, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing 100029, P.R. China.
Department of Respiratory and Critical Care Medicine, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing 100029, P.R. China.
Oncol Lett. 2016 Apr;11(4):2820-2826. doi: 10.3892/ol.2016.4308. Epub 2016 Mar 8.
Pulmonary artery sarcoma (PAS) is an extremely rare and highly malignant tumor that originates in the pulmonary artery. The majority of reported cases of PAS are confirmed by pathological examination subsequent to surgery or by autopsy. The present study reports the clinicopathological characteristics and immunohistochemical phenotypes of three cases of PAS, and aims to facilitate the identification of this lethal disease. In the present study, the data from clinical, histopathological and immunohistochemical examinations of three patients with PAS, whose diagnoses were confirmed by surgical biopsy conducted at the Beijing Anzhen Hospital (Beijing, China) between 2008 and 2012, were retrospectively analyzed. The patients (two women and one man; average age, 41.3 years old) presented with dyspnea on exertion. In addition, two of the patients experienced chest tightness, and one patient experienced intermittent syncope. Computed tomography pulmonary angiography revealed that two of the patients possessed a filling defect in the main, left and right pulmonary arteries, and one patient possessed a filling defect in the right upper pulmonary artery. Macroscopically, the PAS appeared as a mucoid intraluminal or nodular sessile mass spreading along the pulmonary artery. Microscopically, the tumor consisted of spindle cells with fascicular and storiform patterns, and was accompanied by necrosis and stromal myxoid changes. Immunohistochemically, vimentin, desmin and cluster of differentiation 34 were highly expressed in the patient that was diagnosed with intimal sarcoma, while vimentin and α-smooth muscle actin were highly expressed in the other two patients, who were diagnosed with leiomyosarcoma. PAS is often misdiagnosed due to nonspecific clinical manifestations and radiological features. Therefore, the diagnosis of PAS should be based on typical morphological features and immunohistochemical analysis of the tumor tissue.
肺动脉肉瘤(PAS)是一种极为罕见且高度恶性的起源于肺动脉的肿瘤。大多数报道的PAS病例通过手术后续的病理检查或尸检得以确诊。本研究报告了3例PAS的临床病理特征和免疫组化表型,旨在促进对这种致命疾病的识别。在本研究中,回顾性分析了2008年至2012年期间在北京安贞医院(中国北京)通过手术活检确诊的3例PAS患者的临床、组织病理学和免疫组化检查数据。患者(2名女性和1名男性;平均年龄41.3岁)表现为劳力性呼吸困难。此外,2名患者有胸闷症状,1名患者有间歇性晕厥。计算机断层扫描肺动脉造影显示,2名患者在主肺动脉、左肺动脉和右肺动脉有充盈缺损,1名患者在右上肺动脉有充盈缺损。大体上,PAS表现为黏液样腔内或结节状无蒂肿块,沿肺动脉蔓延。显微镜下,肿瘤由呈束状和席纹状排列的梭形细胞组成,并伴有坏死和间质黏液样改变。免疫组化方面,波形蛋白、结蛋白和分化簇34在诊断为内膜肉瘤的患者中高表达,而波形蛋白和α平滑肌肌动蛋白在另外2名诊断为平滑肌肉瘤的患者中高表达。由于临床表现和影像学特征缺乏特异性,PAS常被误诊。因此,PAS的诊断应基于肿瘤组织的典型形态学特征和免疫组化分析。