首页> 美国卫生研究院文献>Journal of Community Hospital Internal Medicine Perspectives >When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma
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When a pulmonary embolism is not a pulmonary embolism: a rare case of primary pulmonary leiomyosarcoma

机译:当肺栓塞不是肺栓塞时:原发性肺平滑肌肉肉瘤的罕见情况

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摘要

Arterial leiomyosarcomas account for up to 21% of vascular leiomyosarcomas, with 56% of arterial leiomyosarcomas occurring in the pulmonary artery. While isolated cases of primary pulmonary artery leiomyosarcoma document survival up to 36 months after treatment, these uncommon, aggressive tumors are highly lethal, with 1-year survival estimated at 20% from the onset of symptoms. We discuss a rare case of a pulmonary artery leiomyosarcoma that was originally diagnosed as a pulmonary embolism (PE). A 72-year-old Caucasian female was initially diagnosed with ‘saddle pulmonary embolism’ based on computerized tomographic angiography of the chest 2 months prior to admission and placed on anticoagulation. Dyspnea escalated, and serial computed tomography scans showed cardiomegaly with pulmonary emboli involving the right and left main pulmonary arteries with extension into the right and left upper and lower lobe branches. An echocardiogram on admission showed severe pulmonary hypertension with a pulmonary artery pressure of 82.9 mm Hg, and a severely enlarged right ventricle. Respiratory distress and multiorgan failure developed and, unfortunately, the patient expired. Autopsy showed a lobulated, yellow mass throughout the main pulmonary arteries measuring 13 cm in diameter. The mass extended into the parenchyma of the right upper lobe. On microscopy, the mass was consistent with a high-grade primary pulmonary artery leiomyosarcoma. Median survival of patients with primary pulmonary artery leiomyosarcoma without surgery is one and a half months, and mortality is usually due to right-sided heart failure. Pulmonary artery leiomyosarcoma is a rare but highly lethal disease commonly mistaken for PE. Thus, we recommend clinicians to suspect this malignancy when anticoagulation fails to relieve initial symptoms. In conclusion, early detection and suspicion of pulmonary artery leiomyosarcoma should be considered in patients refractory to anticoagulation, prompting initiation of early intervention.
机译:动脉平滑肌肉瘤占血管平滑肌肉瘤的21%,其中56%发生在肺动脉。尽管孤立的原发性肺动脉平滑肌肉瘤病例在治疗后可存活至36个月,但这些罕见的侵袭性肿瘤具有很高的致死性,从症状发作开始,一年的存活率估计为20%。我们讨论了一种罕见的肺动脉平滑肌肉瘤病例,最初被诊断为肺栓塞(PE)。入院前2个月,根据胸部计算机X线断层血管造影术,最初诊断出一名72岁的白种女性为“鞍型肺栓塞”,并进行了抗凝治疗。呼吸困难升级,并且连续的计算机体层摄影术扫描显示心脏肿大,肺栓塞累及左右主要肺动脉,并延伸到左右上,下叶分支。入院时的超声心动图显示严重肺动脉高压,肺动脉压为82.9 mm Hg,右心室严重增大。出现呼吸窘迫和多器官功能衰竭,不幸的是,患者死亡。尸检显示整个肺主动脉直径为13厘米,呈小叶状黄色团块。肿块延伸到右上叶的薄壁组织。在显微镜下,肿物与高度原发性肺动脉平滑肌肉瘤一致。未经手术的原发性肺动脉平滑肌肉瘤患者的中位生存期为一个半月,死亡率通常是由于右侧心力衰竭所致。肺动脉平滑肌肉瘤是一种罕见但高度致死性疾病,通常被误认为PE。因此,我们建议临床医生在抗凝治疗未能缓解最初症状时怀疑这种恶性肿瘤。总之,对于难治性抗凝的患者,应考虑早期发现和怀疑肺动脉平滑肌肉瘤,这促使人们开始进行早期干预。

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