Park J W, Kim J H, Kim W B, Han H J, Choi S B, Yeon J E, Byun K S, Choi S Y
Department of Surgery, Korea University College of Medicine, Seoul, Korea.
Transplant Proc. 2011 Jul-Aug;43(6):2428-30. doi: 10.1016/j.transproceed.2011.05.034.
Invasive pulmonary aspergillosis (IPA) is a rare complication with a high mortality rate after organ transplantation. Early antifungal therapy improves survival. In some cases, surgical resection is necessary for a complete remission. We have reported herein a case of sustained (but stationary) IPA cured by the modulation of immunosuppression with discontinuation of antifungal therapy.
A 34-year-old man underwent liver transplantation experiencing are early bile leak and an acute rejection episode. Steroid pulse therapy was accompanied by intensified immunosuppression. After a week he developed intermittent hemoptysis, which was treated with antibiotics due to a diagnosis of pneumonia by chest X ray. Meanwhile the bile leak progressed to a huge biloma at reoperation 3 weeks after the initial operation he was converted from a choledochocholedochostomy to a hepaticojejunostomy. After 1 week, follow-up chest X ray showed the lesion had progressed to form an abscess. Subsequent chest computed tomography (CT) detected a pulmonary mass with internal necrosis and CT-guided lung biopsy revealed Aspergillus fumigatus on isolation. Antifungal therapy with voriconazole and/or amphotericin B for 3 months stopped disease progression but the lesion was sustained. We stopped antifungal therapy due to side effects and reduced the intensity of immunosuppression. Follow-up chest CT 5 months later showed improvement with a persistent cavitary lesion containing a fungal ball. However, after 9 months, there was no focal lesion in either lung. This unusual case of IPA was cured by reducing immunosuppression without antifungal therapy.
IPA should be eradicated with prompt antifugal therapy, but stationary IPA can be observed cautiously while reducing immunosuppression.
侵袭性肺曲霉病(IPA)是器官移植后一种罕见但死亡率高的并发症。早期抗真菌治疗可提高生存率。在某些情况下,手术切除对于完全缓解是必要的。我们在此报告了一例通过调整免疫抑制并停用抗真菌治疗而治愈的持续性(但静止性)IPA病例。
一名34岁男性接受了肝移植,术后早期出现胆漏和急性排斥反应。类固醇冲击治疗伴随着强化免疫抑制。一周后,他出现间歇性咯血,因胸部X线诊断为肺炎而接受抗生素治疗。与此同时,胆漏在初次手术后3周再次手术时发展为巨大胆汁瘤,他从胆总管对端吻合术改为肝空肠吻合术。1周后,胸部X线随访显示病变进展形成脓肿。随后的胸部计算机断层扫描(CT)检测到一个有内部坏死的肺部肿块,CT引导下肺活检分离出烟曲霉。伏立康唑和/或两性霉素B抗真菌治疗3个月阻止了疾病进展,但病变持续存在。由于副作用我们停用了抗真菌治疗并降低了免疫抑制强度。5个月后的胸部CT随访显示有所改善,有一个持续的含真菌球的空洞性病变。然而,9个月后,双肺均无局灶性病变。这例不寻常的IPA病例通过降低免疫抑制而未进行抗真菌治疗得以治愈。
IPA应通过及时的抗真菌治疗根除,但对于静止性IPA,在降低免疫抑制的同时可谨慎观察。