Muganlinskaya Nargiz, Guzman Amanda, Dahagam Chanukya, Selinger Stephen R
Department of Medicine, MedStar Franklin Square Medical Center, Baltimore, MD, USA;
No current affiliations.
J Community Hosp Intern Med Perspect. 2015 Dec 11;5(6):29624. doi: 10.3402/jchimp.v5.29624. eCollection 2015.
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.
动脉平滑肌肉瘤占血管平滑肌肉瘤的比例高达21%,其中56%的动脉平滑肌肉瘤发生在肺动脉。虽然有个别原发性肺动脉平滑肌肉瘤病例记录显示治疗后生存期可达36个月,但这些罕见且侵袭性强的肿瘤具有高度致死性,从症状出现开始计算,1年生存率估计为20%。我们讨论一例罕见的最初被诊断为肺栓塞(PE)的肺动脉平滑肌肉瘤病例。一名72岁的白种女性在入院前2个月基于胸部计算机断层血管造影最初被诊断为“马鞍形肺栓塞”并接受抗凝治疗。呼吸困难加剧,系列计算机断层扫描显示心脏扩大,肺栓塞累及左右主肺动脉并延伸至左右上下叶分支。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 mmHg,右心室严重扩大。呼吸窘迫和多器官功能衰竭出现,不幸的是,患者死亡。尸检显示整个主肺动脉有一个分叶状的黄色肿块,直径13 cm。肿块延伸至右上叶实质。显微镜检查显示该肿块符合高级别原发性肺动脉平滑肌肉瘤。未接受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,死亡通常归因于右心衰竭。肺动脉平滑肌肉瘤是一种罕见但高度致死的疾病,常被误诊为PE。因此,我们建议临床医生在抗凝治疗未能缓解初始症状时怀疑这种恶性肿瘤。总之,对于抗凝治疗无效的患者,应考虑早期发现并怀疑肺动脉平滑肌肉瘤,促使尽早开始干预。