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利妥昔单抗治疗疑似肾移植后淋巴组织增生性疾病后发生的隐源性机化性肺炎。

Cryptogenic organizing pneumonia after rituximab therapy for presumed post-kidney transplant lymphoproliferative disease.

机构信息

Division of Nephrology, Montreal Children's Hospital, McGill University, 2300, rue Tupper E-222, Montréal, Québec, H3P 1P3, Canada.

出版信息

Pediatr Nephrol. 2010 Jun;25(6):1163-7. doi: 10.1007/s00467-010-1447-8. Epub 2010 Feb 6.

Abstract

Cryptogenic organizing pneumonia (COP, formerly bronchiolitis obliterans organizing pneumonia) is rare in children. We describe an 11-year-old girl with Epstein-Barr virus (EBV) reactivation/presumed post-transplant lymphoproliferative disease (PTLD) 15 months after undergoing a deceased donor kidney transplantation. Treatment with reduced immunosuppression, ganciclovir, and cytomegalovirus immunoglobulin was complicated by severe graft rejection, prompting therapy with methylprednisolone, anti-thymocyte globulin and four weekly doses of rituximab (total 1500 mg/m(2)). Tacrolimus- and prednisone-based anti-rejection prophylaxis was complemented with low-dose sirolimus. When the lactate dehydrogenase and uric acid levels rose 10 weeks after the first rituximab infusion and bilateral pulmonary nodules were detected by computerized tomography, recurrence of PTLD was suspected. Open lung biopsy of the clinically asymptomatic patient identified the nodules as COP, characterized by abundant CD3(+) T-cells, few B-cells, and the absence of EBV, cytomegalovirus, or adenovirus antigens. With normalization of the peripheral B-cell count, EB viremia reappeared and persisted, despite minimal immunosuppression. Four years later, the patient was diagnosed with classical Hodgkin lymphoma-type PTLD with multiple pulmonary and abdominal nodes. This first report of rituximab-associated, pediatric COP highlights the risk of pulmonary complications after treatment with B-cell depleting agents in solid organ transplant recipients, and the importance of a histopathologic diagnosis and vigilant follow-up of such lesions.

摘要

隐源性机化性肺炎(COP,既往称为闭塞性细支气管炎伴机化性肺炎)在儿童中罕见。我们描述了一例 11 岁女孩,在接受尸体供肾移植 15 个月后发生 EBV 再激活/推定移植后淋巴组织增生性疾病(PTLD)。减少免疫抑制、更昔洛韦和巨细胞病毒免疫球蛋白的治疗因严重移植物排斥而复杂化,促使使用甲基强的松龙、抗胸腺细胞球蛋白和利妥昔单抗(共 1500mg/m2)每周 4 次治疗。他克莫司和泼尼松的抗排斥预防方案辅以低剂量西罗莫司。在首次利妥昔单抗输注后 10 周,乳酸脱氢酶和尿酸水平升高,且计算机断层扫描检测到双侧肺结节,怀疑 PTLD 复发。对无症状患者进行开胸肺活检,发现结节为 COP,其特征是 CD3(+)T 细胞丰富,B 细胞较少,且缺乏 EBV、巨细胞病毒或腺病毒抗原。尽管免疫抑制最小,但外周 B 细胞计数正常化后,EB 病毒血症再次出现并持续存在。4 年后,该患者被诊断为经典霍奇金淋巴瘤型 PTLD,伴有多个肺和腹部淋巴结。这是首例关于利妥昔单抗相关儿科 COP 的报告,强调了在实体器官移植受者中使用 B 细胞耗竭剂治疗后发生肺部并发症的风险,以及对这些病变进行组织病理学诊断和密切随访的重要性。

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