结节性硬化
TSC1
TSC2
淋巴管平滑肌瘤病
突变
医学
生物
遗传学
病理
基因
PI3K/AKT/mTOR通路
细胞凋亡
作者
D A Muzykewicz,Aditya Sharma,Victorine V. Muse,Adam L. Numis,Jayaraj Rajagopal,E Thiele
标识
DOI:10.1136/jmg.2008.065342
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.
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