Alveolar capillary dysplasia: Lung biopsy diagnosis, nitric oxide responsiveness, and bronchial generation count

被引:24
作者
Sirkin, W
OHare, BP
Cox, PN
Perrin, D
Cutz, E
Silver, MM
机构
[1] HOSP SICK CHILDREN,DEPT PATHOL,TORONTO,ON M5G 1X8,CANADA
[2] UNIV TORONTO,TORONTO,ON,CANADA
[3] HOSP SICK CHILDREN,DEPT CRIT CARE,TORONTO,ON M5G 1X8,CANADA
来源
PEDIATRIC PATHOLOGY & LABORATORY MEDICINE | 1997年 / 17卷 / 01期
关键词
alveolar capillary dysplasia; fetal lung development; fetal lung vascularization; persistent pulmonary hypertension of newborn; pulmonary hypoplasia;
D O I
10.1080/107710497175083
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Alveolar capillary dysplasia, a rare cause of neonatal pulmonary hypertension characterized by a developmental abnormality in the pulmonary vasculature, was diagnosed by lung biopsy in a male newborn maintained on nitric oxide therapy for 18 days. Autopsy confirmed the pulmonary vascular defect and demonstrated deficient airspace formation. In addition, a bronchial generation count was low, suggesting that the abnormal lung vascular development in this condition represents a special form of pulmonary hypoplasia that starts in early fetal life.
引用
收藏
页码:125 / 132
页数:8
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