Obscure pulmonary artery intimal sarcoma presenting with hemoptysis and pulmonary embolism

IF 0.2 Q4 ONCOLOGY Current problems in cancer. Case reports Pub Date : 2025-03-01 Epub Date: 2025-01-13 DOI:10.1016/j.cpccr.2025.100351
Daniel Cheah , Rachael Wong , Sushan Gupta , Frank Bellafiore , Paramesh Dakshinesh
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Abstract

Pulmonary artery intimal sarcoma (PAIS) is a rare and highly malignant neoplasm that presents similarly to pulmonary embolism. Due to the rarity of presentation and high mortality, there is limited data on its heterogeneous presentation, epidemiology, and treatment. We present a case of pulmonary artery intimal sarcoma mimicking features of pneumonia and pulmonary embolism. Our patient was a 43-year-old non-smoker male with no past medical history who presented with a cough with hemoptysis. Initial CT imaging showed acute right pulmonary embolism with right lung pulmonary infarct. The patient was treated with anticoagulation. On follow-up, he continued to complain of hemoptysis. Repeat CT lung now showed a moderate-sized right hilar mass. Endobronchial ultrasound-guided fine needle aspiration biopsy of the hilar mass with bronchial lavage showed malignant cells with immunohistochemistry positive for vimentin. The patient underwent a right pneumonectomy when he was later diagnosed with pulmonary artery intimal sarcoma. He was subsequently started on epirubicin, ifosfamide, and mesna and is currently on 3-monthly CT surveillance with no disease recurrence.
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隐蔽性肺动脉内膜肉瘤,表现为咯血和肺栓塞
肺动脉内膜肉瘤(PAIS)是一种罕见的高度恶性肿瘤,其表现与肺栓塞相似。由于罕见的表现和高死亡率,关于其异质性表现、流行病学和治疗的数据有限。我们报告一例肺动脉内膜肉瘤,其特征与肺炎及肺栓塞相似。我们的病人是一名43岁的非吸烟男性,无既往病史,表现为咳嗽和咯血。初步CT表现为急性右肺栓塞伴右肺梗死。病人接受了抗凝治疗。在随访中,他继续抱怨咯血。重复CT示右肺门中等大小肿块。超声引导下支气管肺门肿块细针穿刺活检经支气管灌洗显示恶性细胞,免疫组化波形蛋白阳性。当他后来被诊断为肺动脉内膜肉瘤时,接受了右侧全肺切除术。随后开始使用表柔比星、异环磷酰胺和mesna,目前正在进行3个月的CT监测,无疾病复发。
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CiteScore
0.40
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0.00%
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0
审稿时长
96 days
期刊最新文献
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