Division of Pulmonology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Pediatr Pulmonol. 2013 Jan;48(1):91-3. doi: 10.1002/ppul.22528. Epub 2012 Mar 19.
Dyskeratosis congenita (DKC) is a syndrome characterized by immunodeficiency, bone marrow (BM) failure, somatic abnormalities, and predisposition to malignancy, resulting from mutations in proteins involved in maintenance of telomeres. Pulmonary fibrosis resulting in respiratory failure is a serious complication affecting approximately 20% of DKC patients. Pediatric pulmonologists should consider this diagnosis in patients with lung fibrosis and concurrent immunodeficiency or BM failure.
先天性角化不良(DKC)是一种综合征,其特征为免疫缺陷、骨髓(BM)衰竭、躯体异常和恶性肿瘤易感性,由涉及端粒维持的蛋白突变引起。导致呼吸衰竭的肺纤维化是一种严重的并发症,影响约 20%的 DKC 患者。儿科肺病学家应在有肺纤维化且同时存在免疫缺陷或 BM 衰竭的患者中考虑这一诊断。