Department of Radiology, The Affiliated Hospital of Qingdao University, Qingdao, China, 266003.
Department of Radiology, The Affiliated Hospital of Qingdao University, Qingdao, China, 266003.
Am J Med Sci. 2022 Nov;364(5):655-660. doi: 10.1016/j.amjms.2022.05.009. Epub 2022 May 16.
Pulmonary artery intimal sarcomas are very rare and arise from primitive pluripotent mesenchymal cells. They are often misdiagnosed as pulmonary thromboembolism, leading to futile anticoagulation treatment and delayed diagnosis. We present a case of a patient who showed nonspecific pulmonary symptoms and characteristic imaging manifestation. Progressive symptoms and additional imaging led to the suspicion of a pulmonary artery intimal sarcoma, which was finally confirmed by pathological biopsy. This case serves as a reminder to consider pulmonary artery intimal sarcomas in the differential diagnosis of patients with dyspnea and filling defects on computed tomography pulmonary angiography or contrast-enhanced computed tomography.
肺动脉内膜肉瘤非常罕见,起源于原始多能间充质细胞。它们常被误诊为肺血栓栓塞症,导致无效的抗凝治疗和延迟诊断。我们报告了一例表现为非特异性肺部症状和特征性影像学表现的患者。进行性症状和额外的影像学检查提示肺动脉内膜肉瘤的可能性,最终通过病理活检得到证实。这个病例提醒我们,在呼吸困难和 CT 肺动脉造影或增强 CT 上有充盈缺损的患者的鉴别诊断中,应考虑肺动脉内膜肉瘤。