TSC1 and TSC2 mutations in patients with lymphangioleiomyomatosis and tuberous sclerosis complex

被引:52
|
作者
Muzykewicz, D. A. [1 ]
Sharma, A. [2 ]
Muse, V. [2 ]
Numis, A. L. [1 ]
Rajagopal, J. [3 ]
Thiele, E. A. [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Pulm & Crit Care Unit, Boston, MA 02114 USA
关键词
PULMONARY-FUNCTION TESTS; CT; GENE; LYMPHANGIOMYOMATOSIS; IDENTIFICATION; DISEASE; WOMEN;
D O I
10.1136/jmg.2008.065342
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Lymphangioleiomyomatosis (LAM) is a prominent finding in the setting of tuberous sclerosis complex (TSC). Objective: The present study was designed to compare cystic lung changes consistent with LAM in patients with a TSC1 disease-causing mutation, TSC2 disease-causing mutation, or no mutation identified (NMI). Methods and results: We conducted a retrospective review of the chest computed tomography (CT) of 45 female and 20 male patients with TSC and found cysts consistent with LAM in 22 (49%) women and two (10%) men. In the female population, changes consistent with LAM were observed in six of 15 (40%) patients with TSC1, 11 of 23 (48%) with TSC2, and five of seven (71%) with NMI. While the predominant size of cysts did not differ across these three groups, TSC2 women with LAM had a significantly greater number of cysts than did TSC1 patients (p = 0.010). Conclusions: These findings suggest a higher rate of LAM in TSC1 than previously recognised, as well as a fundamental difference in CT presentation between TSC1 and TSC2.
引用
收藏
页码:465 / 468
页数:4
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