Department of Respiratory Medicine II, Beijing Children's Hospital affiliated to Capital Medical University, National Center for Children's Health, Beijing, P.R. China.
Department of Pathology, Beijing Children's Hospital affiliated to Capital Medical University, National Center for Children's Health, Beijing, P.R. China.
Pediatr Pulmonol. 2020 Jun;55(6):1481-1486. doi: 10.1002/ppul.24781. Epub 2020 Apr 15.
Combined methylmalonic acidemia and homocysteinemia is a genetically heterogeneous disorder of cobalamin (cbl; vitamin B12) metabolism, which consists of five subtypes including cblC, cblD, cblF, cblJ, and cblX deficiencies. The purpose of this study is to summarize new clinical features mainly diffuse alveolar hemorrhage (DAH) in cblC deficiency.
We made a retrospective analysis of four pediatric patients diagnosed with DAH and pulmonary microangiopathy due to cblC deficiency between January 2017 and December 2018 in Beijing Children's Hospital.
This study describes four patients with their ages ranging from 4 years 2 months to 7 years 6 months with cblC deficiency who developed late-onset diffuse lung disease (DLD). Of these, the first three patients presented predominantly with DAH, and the last patient with pulmonary microangiopathy confirmed by thoracoscopic lung biopsy. All patients were accompanied by pulmonary arterial hypertension (PAH), two accompanied by respiratory failure, and two accompanied by moderate megaloblastic anemia. Diffuse ground-glass opacification and poorly defined ground-glass centrilobular nodules were seen on high-resolution computed tomography in one patient and three patients, respectively. All patients were suspected of having idiopathic pulmonary hemosiderosis or interstitial lung disease at other hospitals. All of them received treatment with corticosteroid before admission, but the symptoms did not improve. Moreover, all patients carried compound heterozygous mutations (c.80A>G, c.609G>A) in MMACHC and improved significantly after being treated for cblC deficiency and PAH.
CblC deficiency should be considered in the differential diagnosis of DAH especially with PAH, and pulmonary microangiopathy be the main reason of DLD in these patients.
甲基丙二酸血症和同型半胱氨酸血症是一种遗传异质性钴胺素(cbl;维生素 B12)代谢紊乱,包括 cblC、cblD、cblF、cblJ 和 cblX 缺乏五种亚型。本研究旨在总结 cblC 缺乏症的新临床特征,主要为弥漫性肺泡出血(DAH)。
对 2017 年 1 月至 2018 年 12 月在北京儿童医院诊断为 cblC 缺乏症导致 DAH 和肺微血管病的 4 例儿科患者进行回顾性分析。
本研究描述了 4 例 cblC 缺乏症患儿,年龄为 4 岁 2 个月至 7 岁 6 个月,发生迟发性弥漫性肺病(DLD)。其中前 3 例以 DAH 为主,最后 1 例经胸腔镜肺活检证实为肺微血管病。所有患者均伴有肺动脉高压(PAH),2 例伴有呼吸衰竭,2 例伴有中度巨幼细胞性贫血。1 例患者高分辨率 CT 显示弥漫性磨玻璃混浊,3 例患者显示边界不清的磨玻璃中心性结节。所有患者在其他医院均被怀疑为特发性肺含铁血黄素沉着症或间质性肺病,均在入院前接受了皮质类固醇治疗,但症状无改善。此外,所有患者均携带 MMACHC 基因的复合杂合突变(c.80A>G、c.609G>A),在接受 cblC 缺乏和 PAH 治疗后,病情明显改善。
在 DAH 尤其是伴有 PAH 的鉴别诊断中应考虑 cblC 缺乏症,在这些患者中,肺微血管病是 DLD 的主要原因。