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首页> 外文期刊>Cureus. >A Rare Case of Inflammatory Myofibroblastic Tumor Causing Left Pulmonary Artery Stenosis and Successfully Treated with Localized Radiotherapy in a Patient with Perinuclear Antineutrophil Cytoplasmic Antibody Vasculitis
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A Rare Case of Inflammatory Myofibroblastic Tumor Causing Left Pulmonary Artery Stenosis and Successfully Treated with Localized Radiotherapy in a Patient with Perinuclear Antineutrophil Cytoplasmic Antibody Vasculitis

机译:罕见的炎性肌纤维细胞肿瘤,导致肺动脉狭窄,并在患者中成功治疗患者患者患者患者患者细胞质抗体抗体血管炎

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摘要

Inflammatory myofibroblastic tumor (IMT) of the lung is a rare neoplasm that commonly behaves in an indolent fashion and is generally treated with complete surgical excision. The management of unresectable IMT presents a significant challenge, especially in cases with multiple comorbidities, and a consensus has yet to be reached on the most appropriate first-line modality. We present a case of unresectable IMT causing severe stenosis of the left pulmonary artery in a patient on immunosuppressive therapy for perinuclear antineutrophil cytoplasmic antibody vasculitis. The patient was successfully treated with localized radiotherapy to a total dose of 45 Gy in five weeks, and has been followed for more than seven years since treatment. In this case report, we review the pertinent literature and illustrate the difficulties in diagnosing and treating rare neoplasms in a patient with significant medical comorbidities.
机译:肺炎的炎症肌纤维肿瘤(IMT)是一种罕见的肿瘤,通常以惰性的方式表现,并且通常用完全手术切除治疗。不可切除的IMT管理提出了重大挑战,特别是在多种合并症的情况下,尚未以最合适的一线方式达成共识。我们提出了一种在免疫抑制治疗患者患者患者患者左肺动脉的严重狭窄的情况下,提出了不可切除的IMT的情况。患者在五周内成功地用局部放射治疗到总剂量为45吨,并在待遇以来超过七年。在本案中,我们审查了相关文献,并说明了诊断和治疗具有重要医疗合并症的患者稀有肿瘤的困难。

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