Asano Takeru, Fujii Nobuharu, Niiya Daigo, Nishimori Hisakazu, Fujii Keiko, Matsuoka Ken-Ichi, Ichimura Koichi, Hamada Toshihisa, Kondo Eisei, Maeda Yoshinobu, Tanimoto Yasushi, Shinagawa Katsuji, Tanimoto Mitsune
Department of Hematology, Oncology, and Respiratory Medicine, Okayama University Hospital, Okayama, Japan.
Department of Hematology, Oncology, and Respiratory Medicine, Okayama University Hospital, Okayama, Japan ; Division of Transfusion, Okayama University Hospital, Okayama, Japan.
Springerplus. 2014 Jan 2;3:3. doi: 10.1186/2193-1801-3-3. eCollection 2014.
Pulmonary complications in patients with hematological malignancies are often caused by infection but are sometimes associated with an underlying disease such as organizing pneumonia (OP). Here, we report a case of life-threatening steroid-resistant OP associated with myelodysplastic syndrome (MDS) and successfully performed allogeneic hematopoietic cell transplantation (HSCT). A 33-year-old female with refractory anemia with excess blasts-1 that had progressed from refractory anemia with ringed sideroblasts and concomitant Sweet's syndrome was admitted. Multiple pulmonary infiltrates were revealed on a chest computed tomography scan, which progressively worsened even after chemotherapy and corticosteroid therapy. No evidence of infection was observed in bronchoalveolar lavage fluid. A histological examination of a transbronchial lung biopsy specimen showed lymphocyte invasion with fibrosis, indicating that the pulmonary infiltrates were OP associated with MDS. Before transplantation, she suffered from respiratory failure and required oxygen supplementation. She developed idiopathic pneumonitis syndrome on day 61 that responded well to corticosteroid therapy, and the OP pulmonary infiltrates improved gradually after HSCT, She was discharged on day 104 and is well without recurrence of OP or MDS 2 years after HSCT.
血液系统恶性肿瘤患者的肺部并发症通常由感染引起,但有时与潜在疾病如机化性肺炎(OP)有关。在此,我们报告一例与骨髓增生异常综合征(MDS)相关的危及生命的类固醇抵抗性OP病例,并成功进行了异基因造血细胞移植(HSCT)。一名33岁女性因难治性贫血伴原始细胞增多-1从伴有环形铁粒幼细胞的难治性贫血进展而来,并伴有Sweet综合征入院。胸部计算机断层扫描显示多处肺部浸润,即使在化疗和皮质类固醇治疗后仍逐渐恶化。支气管肺泡灌洗液中未观察到感染迹象。经支气管肺活检标本的组织学检查显示淋巴细胞浸润伴纤维化,表明肺部浸润是与MDS相关的OP。移植前,她出现呼吸衰竭,需要吸氧。她在第61天发生特发性肺炎综合征,对皮质类固醇治疗反应良好,HSCT后OP肺部浸润逐渐改善,她于第104天出院,HSCT后2年情况良好,未出现OP或MDS复发。