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Clinicopathological and immunohistochemical features of pulmonary artery sarcoma: A report of three cases and review of the literature

机译:肺动脉肉瘤的临床病理及免疫组化特征:三例报告并文献复习

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摘要

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 -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.
机译:肺动脉肉瘤(PAS)是一种极为罕见且高度恶性的肿瘤,起源于肺动脉。报道的大多数PAS病例是通过手术后的病理检查或尸检确认的。本研究报告了三例PAS的临床病理特征和免疫组化表型,旨在促进这种致命疾病的鉴定。在本研究中,回顾性分析了2008年至2012年在北京安贞医院(中国北京)进行的手术活检证实的3例PAS患者的临床,组织病理学和免疫组化检查数据。患者(两名妇女和一名男子;平均年龄为41.3岁)因劳累而出现呼吸困难。此外,其中两名患者出现胸闷,一名患者出现间歇性晕厥。计算机断层扫描肺血管造影显示,其中两名患者在主,左,右肺动脉有充盈缺损,而一名患者在右上肺动脉具有充盈缺损。宏观上,PAS表现为沿肺动脉扩散的粘液腔内或结节性无蒂肿块。在显微镜下,肿瘤由纺锤形细胞组成,具有束状和星​​形结构,并伴有坏死和间质粘液样变化。在免疫组织化学中,波形蛋白,结节蛋白和分化簇34在诊断为内膜肉瘤的患者中高表达,而波形蛋白和-平滑肌肌动蛋白在其他两名诊断为平滑肌肉瘤的患者中高表达。由于非特异性的临床表现和影像学特征,常会误诊PAS。因此,PAS的诊断应基于肿瘤组织的典型形态特征和免疫组织化学分析。

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