Labžentytė Violeta, Zemnickienė Silvija, Danila Edvardas, Šileikienė Virginija, Zablockis Rolandas, Gruslys Vygantas
Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Clinic of Infectious and Chest Diseases, Dermatovenereology and Allergology, Vilnius University, Lithuania.
Acta Med Litu. 2016;23(1):54-59. doi: 10.6001/actamedica.v23i1.3270.
We report a case of a patient with acute myeloid leukaemia whose treatment with bone marrow transplantation (BMT) was followed by chronic graft versus host disease (GVHD) with lung involvement and bronchiectasis. This report illustrates an unusual course of a fast progression of the bronchiectasis due to BMT. A 33-year-old female was diagnosed with acute myeloid leukaemia. An allogeneic BMT was performed. One month after the transplantation, acute GVHD with skin involvement occurred. Treatment with prednisolone and mycophenolate mofetil (MMF) has been started. Nine months later, the patient was examined by a pulmonologist due to progressive dyspnoea. A pulmonary computed tomography (CT) scan showed normal parenchyma of the lungs and no changes to the bronchi. A CT scan performed 7 months later revealed bronchiectasis for the first time. No clinical response was associated with the treatment and the patient's respiratory status progressively deteriorated. During the final hospitalization, a CT scan performed 1 year later revealed huge cystic bronchiectasis in both lungs. Despite the prophylaxis and treatment of GVHD and aggressive antimicrobial therapy, the patient died one year after the diagnosis of bronchiectasis. This case demonstrates that a fast and fatal course of bronchiectasis, that occurs after BMT, should always be considered as a possible manifestation of chronic graft versus host disease (cGVHD) following allogeneic BMT.
我们报告了一例急性髓系白血病患者,其接受骨髓移植(BMT)治疗后发生了慢性移植物抗宿主病(GVHD),累及肺部并出现支气管扩张。本报告阐述了因BMT导致支气管扩张快速进展的不寻常病程。一名33岁女性被诊断为急性髓系白血病,接受了异基因BMT。移植后1个月,出现了累及皮肤的急性GVHD,开始使用泼尼松龙和霉酚酸酯(MMF)进行治疗。9个月后,由于进行性呼吸困难,患者接受了肺科医生的检查。肺部计算机断层扫描(CT)显示肺实质正常,支气管无变化。7个月后进行的CT扫描首次显示支气管扩张。治疗无临床反应,患者的呼吸状况逐渐恶化。在最后一次住院期间,1年后进行的CT扫描显示双肺出现巨大的囊性支气管扩张。尽管对GVHD进行了预防和治疗,并积极进行了抗菌治疗,但患者在诊断为支气管扩张1年后死亡。该病例表明,BMT后发生的快速且致命的支气管扩张病程,应始终被视为异基因BMT后慢性移植物抗宿主病(cGVHD)的一种可能表现。