John Corbyn Cravero, Laith Wahab, Dirk T Wilson, Ali Alani, Arthur Bredeweg, Roberto Aguirre
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The patient was transferred to the medical ICU for tPA administration but developed worsening hypoxic respiratory failure and was transferred to an outside hospital for expert surgical consultation and thrombectomy. Intraoperative reports during thrombectomy commented on a mass within the pulmonary artery. Subsequent pathology showed a high-grade sarcoma. The patient was started on adjuvant chemotherapy with doxorubicin, ifosfamide, and MESNA; however, due to multiple comorbidities, the patient ultimately succumbed to her illness.</p><p><strong>Conclusion: </strong>This case underscores the diagnostic difficulty in distinguishing pulmonary artery sarcomas from a PE, especially in the presence of other confounders and biases.</p>","PeriodicalId":9625,"journal":{"name":"Case Reports in Oncology","volume":"17 1","pages":"1294-1300"},"PeriodicalIF":0.7000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11556859/pdf/","citationCount":"0","resultStr":"{\"title\":\"High-Grade Sarcoma of the Pulmonary Artery That Mimicked a Pulmonary Embolism in a 39-Year-Old Patient with Recurrent Miscarriages: A Case Report.\",\"authors\":\"John Corbyn Cravero, Laith Wahab, Dirk T Wilson, Ali Alani, Arthur Bredeweg, Roberto Aguirre\",\"doi\":\"10.1159/000542052\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Primary pulmonary artery sarcoma is a rare malignancy with a poor prognosis, undefined treatment guidelines, and is often mistaken for a pulmonary embolism (PE) based on similar clinical presentation and radiographic findings.</p><p><strong>Case presentation: </strong>We present a case of a 39-year-old female with a past medical history of recurrent miscarriages who presented with a chief complaint of dyspnea. Due to a history of recurrent miscarriages, a predisposing coagulopathic condition was suspected for a PE. A V/Q scan showed high probability for a PE with bilateral perfusion defects. Subsequent CT angiographic imaging of the chest was read as positive for a massive PE. The patient was transferred to the medical ICU for tPA administration but developed worsening hypoxic respiratory failure and was transferred to an outside hospital for expert surgical consultation and thrombectomy. Intraoperative reports during thrombectomy commented on a mass within the pulmonary artery. Subsequent pathology showed a high-grade sarcoma. 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引用次数: 0
摘要
导言:原发性肺动脉肉瘤是一种罕见的恶性肿瘤,预后较差,治疗指南尚未明确,由于临床表现和影像学检查结果相似,常被误诊为肺栓塞(PE):我们接诊了一例 39 岁女性患者,既往有反复流产病史,主诉为呼吸困难。由于有复发性流产病史,她被怀疑患有易发生凝血病变的 PE。V/Q 扫描显示,双侧灌注缺损的 PE 可能性很高。随后的胸部 CT 血管造影显示大面积 PE 阳性。患者被转入内科重症监护室接受 tPA 治疗,但缺氧性呼吸衰竭恶化,于是被转到外院接受专家外科会诊和血栓切除术。血栓切除术的术中报告显示肺动脉内有肿块。随后的病理结果显示为高级别肉瘤。患者开始接受多柔比星、伊福酰胺和MESNA的辅助化疗;然而,由于多种并发症,患者最终因病去世:本病例强调了区分肺动脉肉瘤和肺动脉高压的诊断难度,尤其是在存在其他混杂因素和偏倚的情况下。
High-Grade Sarcoma of the Pulmonary Artery That Mimicked a Pulmonary Embolism in a 39-Year-Old Patient with Recurrent Miscarriages: A Case Report.
Introduction: Primary pulmonary artery sarcoma is a rare malignancy with a poor prognosis, undefined treatment guidelines, and is often mistaken for a pulmonary embolism (PE) based on similar clinical presentation and radiographic findings.
Case presentation: We present a case of a 39-year-old female with a past medical history of recurrent miscarriages who presented with a chief complaint of dyspnea. Due to a history of recurrent miscarriages, a predisposing coagulopathic condition was suspected for a PE. A V/Q scan showed high probability for a PE with bilateral perfusion defects. Subsequent CT angiographic imaging of the chest was read as positive for a massive PE. The patient was transferred to the medical ICU for tPA administration but developed worsening hypoxic respiratory failure and was transferred to an outside hospital for expert surgical consultation and thrombectomy. Intraoperative reports during thrombectomy commented on a mass within the pulmonary artery. Subsequent pathology showed a high-grade sarcoma. The patient was started on adjuvant chemotherapy with doxorubicin, ifosfamide, and MESNA; however, due to multiple comorbidities, the patient ultimately succumbed to her illness.
Conclusion: This case underscores the diagnostic difficulty in distinguishing pulmonary artery sarcomas from a PE, especially in the presence of other confounders and biases.