Coffey M J, Fantone J, Stirling M C, Lynch J P
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109-0360.
Am Rev Respir Dis. 1992 Jun;145(6):1487-90. doi: 10.1164/ajrccm/145.6.1487.
Pulmonary mucormycosis is a rare and almost invariably fatal complication that can occur in the context of severe deficits in host defenses. Antemortem diagnosis is difficult and requires a high index of suspicion together with invasive diagnostic techniques. Mucor species exhibit a pronounced affinity to invade vessels; mucormycosis involving the pulmonary vasculature has rarely been documented antemortem, and survival in this context has been rare. In this report, we describe a patient with chronic renal failure and systemic lupus erythematosus who developed extensive invasion of the left main pulmonary artery by mucormycosis. Chest computed tomographic (CT) scans and pulmonary arteriogram demonstrated a massive pseudoaneurysm of the left pulmonary artery; these radiographic findings have not previously been described in mucormycosis. Aggressive combination therapy, employing preoperative amphotericin B (AmB) followed by surgical resection (pneumonectomy) and a full course of AmB, was curative. This favorable outcome supports the role of surgery as adjunctive therapy, and it underscores the need for early diagnosis and aggressive treatment.
肺毛霉菌病是一种罕见且几乎总是致命的并发症,可发生在宿主防御严重缺陷的情况下。生前诊断困难,需要高度的怀疑指数以及侵入性诊断技术。毛霉菌种对血管侵袭具有明显的亲和力;累及肺血管的毛霉菌病生前很少有记录,在这种情况下存活也很罕见。在本报告中,我们描述了一名患有慢性肾衰竭和系统性红斑狼疮的患者,其左主肺动脉被毛霉菌病广泛侵袭。胸部计算机断层扫描(CT)和肺动脉造影显示左肺动脉有巨大假性动脉瘤;这些影像学表现此前在毛霉菌病中尚未有过描述。采用术前两性霉素B(AmB),随后进行手术切除(肺切除术)及全程AmB的积极联合治疗取得了治愈效果。这一良好结果支持了手术作为辅助治疗的作用,并强调了早期诊断和积极治疗的必要性。