Bandyopadhyay Debabrata, Panchabhai Tanmay S, Bajaj Navkaranbir S, Patil Pradnya D, Bunte Matthew C
Department of Thoracic Medicine, Geisinger Medical Center, Danville, PA, USA.
Norton Thoracic Institute, St Joseph's Medical Center, Phoenix, AZ, USA.
J Thorac Dis. 2016 Sep;8(9):2592-2601. doi: 10.21037/jtd.2016.08.89.
Primary pulmonary artery sarcoma (PPAS) is a rare tumor that mimics pulmonary thromboembolism (PE). Similarities to PE can delay the diagnosis and misguide the treatment of PPAS. This study aimed to evaluate tumor characteristics and outcome predictors among those diagnosed with PPAS and misdiagnosed as PE.
From 1991-2010, 10 PPAS cases were available from the Cleveland Clinic (CC) institutional database and another 381 cases were reported in the literature. Patient characteristics, tumor subtypes, diagnostic testing & timing, interventions and clinical outcomes were analyzed. We also noted effects of misdiagnosis as PE and clinical outcome as a result of inappropriate intervention.
Among 391 confirmed cases of PPAS, the mean age at diagnosis was 52±14 years; 55% were male. The median duration of symptoms prior to diagnosis was 100 [interquartile range (IQR), 30-210] days. Nearly half (47%) of PPAS were originally misdiagnosed as PE including 39% that received thrombolytic and/or anticoagulation therapy. For every doubling of time from symptom onset to diagnosis, the odds of death increased by 46% (OR: 1.46, 95% CI: 1.21-1.82; P<0.001). The odds of death (OR: 2.66, 95% CI: 1.58-4.54; P=0.0003) and occurrence of distant metastasis (OR: 2.30, 95% CI: 1.30-4.15; P=0.049) were increased among those who did not receive chemotherapy but chemotherapy did not impact local recurrence. Those with complete resection had a better survival.
PPAS has a radiological appearance similar to PE, which makes accurate and timely diagnosis challenging. More rapid diagnosis may lead to earlier, appropriate surgical treatment and improved outcomes, when combined with adjuvant treatment.
原发性肺动脉肉瘤(PPAS)是一种罕见的肿瘤,与肺血栓栓塞症(PE)相似。与PE的相似性可能会延迟PPAS的诊断并误导其治疗。本研究旨在评估被诊断为PPAS且被误诊为PE的患者的肿瘤特征和预后预测因素。
1991年至2010年期间,克利夫兰诊所(CC)机构数据库中有10例PPAS病例,另有381例病例在文献中报道。分析了患者特征、肿瘤亚型、诊断检查及时间、干预措施和临床结局。我们还记录了误诊为PE的影响以及不适当干预导致的临床结局。
在391例确诊的PPAS病例中,诊断时的平均年龄为52±14岁;55%为男性。诊断前症状的中位持续时间为100天[四分位间距(IQR),30 - 210天]。近一半(47%)的PPAS最初被误诊为PE,其中39%接受了溶栓和/或抗凝治疗。从症状出现到诊断的时间每增加一倍,死亡几率增加46%(OR:1.46,95%CI:1.21 - 1.82;P<0.001)。未接受化疗的患者死亡几率(OR:2.66,95%CI:1.58 - 4.54;P = 0.0003)和远处转移发生率(OR:2.30,95%CI:1.30 - 4.15;P = 0.049)增加,但化疗对局部复发无影响。完全切除的患者生存情况较好。
PPAS的影像学表现与PE相似,这使得准确及时的诊断具有挑战性。更快的诊断可能会带来更早、合适的手术治疗,并在联合辅助治疗时改善结局。