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

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
出处
期刊:Journal of Medical Genetics [BMJ]
卷期号:46 (7): 465-468 被引量:66
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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