Bush Douglas, Sremba Leighann, Lomax Kate, Lipsett Jill, Ketteridge David, Bratkovic Drago, Enchautegui-Colon Yazmin, Weisfeld-Adams James, Galambos Csaba, Lummus Seth, Wartchow Eric, Weinman Jason, Liptzin Deborah R, Baker Peter
Section of Pulmonary Medicine, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
JIMD Rep. 2019;43:71-77. doi: 10.1007/8904_2018_101. Epub 2018 Apr 14.
We describe two cases of neonatal onset interstitial lung disease eventually diagnosed as mucopolysaccharidosis type I (MPS I). In both cases, evaluation led to lung biopsy, pathology review, and identification of glycogen deposition. Pulmonary interstitial glycogenosis (PIG) was considered as a clinical diagnosis in case one; however, further review of electron microscopy (EM) was more consistent with MPS I rather than PIG. Both cases were confirmed to have MPS I by enzyme and molecular analysis. Neonatal interstitial lung disease is an atypical presentation for MPS I which is likely under-recognized. Diagnosis through clinical guidelines and a multidisciplinary approach had a major impact on patient management. The diagnosis of MPS I prompted timely initiation of enzyme replacement therapy (ERT) and the patients ultimately underwent hematopoietic stem cell transplantation (HSCT) to improve symptomatic outcomes. In addition to treatment, immediate precautionary recommendations were made to avoid potentially catastrophic outcomes associated with cervical instability. These cases add to the clinical spectrum of MPS I in the newborn period. They further illustrate the difficulties in early recognition of the disease, and importance of a definitive diagnosis of MPS I in infants with interstitial lung disease.
我们描述了两例最终被诊断为I型黏多糖贮积症(MPS I)的新生儿期起病的间质性肺疾病病例。在这两例病例中,评估均导致了肺活检、病理检查以及糖原沉积的鉴定。在第一例病例中,临床诊断考虑为肺间质糖原沉积症(PIG);然而,进一步的电子显微镜(EM)检查结果更符合MPS I而非PIG。两例病例均通过酶学和分子分析确诊为MPS I。新生儿间质性肺疾病是MPS I的一种非典型表现,可能未得到充分认识。通过临床指南和多学科方法进行诊断对患者管理产生了重大影响。MPS I的诊断促使及时开始酶替代疗法(ERT),患者最终接受了造血干细胞移植(HSCT)以改善症状结局。除了治疗外,还立即提出了预防性建议,以避免与颈椎不稳相关的潜在灾难性后果。这些病例拓宽了新生儿期MPS I的临床谱。它们进一步说明了早期识别该疾病的困难,以及对间质性肺疾病婴儿进行MPS I明确诊断的重要性。