Lung-transplantation for Williams-Campbell syndrome

被引:16
作者
Palmer, SM
Layish, DT
Kussin, PS
Oury, T
Davis, RD
Tapson, VF
机构
[1] Duke Univ, Med Ctr, Div Pulm & Crit Care Med, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Div Thorac Surg, Dept Surg, Durham, NC 27710 USA
关键词
bronchiectasis; congenital; lung transplantation;
D O I
10.1378/chest.113.2.534
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Williams-Campbell syndrome is a rare disorder characterized by a deficiency of cartilage in subsegmental bronchi leading to distal airway collapse and bronchiectasis. We report the first case of lung transplantation in a patient with end-stage lung disease secondary to Williams-Campbell syndrome. Although the patient did not have proximal airway collapse prior to transplantation, his posttransplant course was complicated by the development of bronchomalacia of the right and left mainstem bronchi. The patient experienced recurrent pulmonary infections and died of bacterial pneumonia 1 year after transplantation, Autopsy revealed cartilage deficiency in both right and left mainstem bronchi. A hypothesis may be made that a combination of proximal cartilage deficiency and posttransplant ail-way ischemia led to the development of bronchomalacia after lung transplantation. Thus, in contrast to previous reports, the cartilage deficiency in Williams-Campbell syndrome can involve both proximal and distal airways. Consequently, bilateral sequential lung transplantation may not be an effective therapeutic option in patients with this syndrome.
引用
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页码:534 / 537
页数:4
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