COR-PULMONALE AS A COMPLICATION OF METHYLMALONIC ACIDEMIA AND HOMOCYSTINURIA (CBL-C-TYPE)

被引:41
作者
BRANDSTETTER, Y
WEINHOUSE, E
SPLAINGARD, ML
TANG, TT
机构
[1] MED COLL WISCONSIN,DEPT PEDIAT,MACC FUND RES CTR,8701 WATERTOWN PLANK RD 3050,MILWAUKEE,WI 53226
[2] MED COLL WISCONSIN,CARDIOL SECT,MILWAUKEE,WI 53226
[3] MED COLL WISCONSIN,PULM SECT,MILWAUKEE,WI 53226
[4] MED COLL WISCONSIN,DEPT PATHOL,MILWAUKEE,WI 53226
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 36卷 / 02期
关键词
congenital metabolic disorders; pulmonary coagulopathy; thromboembolic phenomenon;
D O I
10.1002/ajmg.1320360208
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report an infant with a bronchiolitis-like illness and rapid deterioration who developed a cor pulmonale-like picture with a dilated righ ventricle. Urinary organic acid assays established a probable diagnosis of Cbl-C-type methylmalonic aciduria, later confirmed by complementation studies. Despite medical intervention and cyanocobalamin treatment the patient died on his tenth hospital day. Postmortem examination showed the presence of thromboemboli in the pulmonary circulation. We hypothesize that acute cor pulmonale developed in this infant secondary to thromboembolism of his pulmonary circulation. A review of the literature shows that thromboembolism may be a part of this disease process.
引用
收藏
页码:167 / 171
页数:5
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