Zhao Qin-Hua, Wu Wen-Hui, Fu Li-Jun, Wang Lan
Department of Pulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, 507, Zhengmin Road, Shanghai 200433, China.
Department of Cardiology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, 1678, Dongfang Road, Shanghai 200127, China.
Eur Heart J Case Rep. 2021 Jun 30;5(6):ytab251. doi: 10.1093/ehjcr/ytab251. eCollection 2021 Jun.
Cobalamin C (cbl-C) defect is an inherited autosomal recessive disorder that commonly affects the central nervous system of infants. Severe pulmonary hypertension (PH) and diffuse lung lesions are unusual clinical manifestations, especially among adults.
A 25-year-old man with hypoxaemia, diffuse lung lesions, and PH, suddenly developed nausea, vomiting, headache, and worsening of dyspnoea. Metabolic screening showed elevated serum levels of methylmalonic acid and homocysteine, and genetic testing revealed gene mutations. He was eventually diagnosed with severe PH secondary to cbl-C defect and was successfully managed with vitamin B12, betaine, L-carnitine, folate, as well as ambrisentan and sildenafil.
cbl-C is a rare cause of PH and can present with severe PH and diffuse lung lesions in adults. Given that the condition is treatable, a careful metabolic screening should be considered when a diagnosis of PH is made.
钴胺素C(cbl-C)缺陷是一种常影响婴儿中枢神经系统的常染色体隐性遗传病。严重肺动脉高压(PH)和弥漫性肺部病变是不常见的临床表现,尤其在成年人中。
一名25岁男性,伴有低氧血症、弥漫性肺部病变和PH,突然出现恶心、呕吐、头痛及呼吸困难加重。代谢筛查显示血清甲基丙二酸和同型半胱氨酸水平升高,基因检测发现基因突变。他最终被诊断为继发于cbl-C缺陷的严重PH,并通过维生素B12、甜菜碱、左旋肉碱、叶酸以及安立生坦和西地那非成功治疗。
cbl-C是PH的罕见病因,可在成人中表现为严重PH和弥漫性肺部病变。鉴于该病可治疗,在诊断PH时应考虑进行仔细的代谢筛查。