Li Shuqiang, Zhang Yushi, Wei Jinxing, Zhang Xuepei
Department of Urology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450000, P.R. China.
Department of Urology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, P.R. China.
Oncol Lett. 2017 Dec;14(6):7085-7090. doi: 10.3892/ol.2017.7079. Epub 2017 Sep 27.
Tuberous sclerosis complex-associated renal angiomyolipoma (TSC-RAML) confers a high risk of bleeding and even mortality. However, data on TSC-RAML in Chinese pedigrees is extremely lacking. The present study aimed to investigate its clinical and genetic characteristics by obtaining a detailed medical history from 6 probands and their family members, and reassessing blood tests, computed tomography and renal dynamic imaging examinations that were conducted in the TSC-RAML patients. The TSC1/TSC2 mutation was detected in 2 families. A total of 3 TSC-RAML patients underwent partial nephrectomy due to a high bleeding risk, and the other 2 were treated with everolimus. The remaining 6 TSC-RAML patients received no clinical intervention and only had clinical follow-uzp. It was found that nearly 37% (18/49) were TSC patients, with the mean ± standard deviation diagnostic age being 34.22±17.73 years old in the 6 pedigrees, 61% (11/18) of whom suffered from TSC-RAML. In the 11 TSC-RAML patients, the maximum diameter of the tumor ranged between 1.20 and 32.50 cm (mean ± standard deviation, 11.48±8.40 cm), the unilateral glomerular filtration rate ranged between 27.20 and 60.10 ml/min (mean ± standard deviation, 42.55±9.73 ml/min), the serum creatinine level ranged between 40.00 and 90.00 µmol/l (mean ± standard deviation, 64.84±16.15 µmol/l) and the hemoglobin concentration ranged between 76.00 and 140.00 g/l (mean ± standard deviation, 107.73±21.04 g/l). Pathogenic mutations of TSC1 (c.733C>T) and TSC2 (c.788_789insC) were detected in family B and C, respectively, as well as certain non-pathogenic mutations, with the maximum diameter of TSC-RAML being 0 cm and 10.3 cm in the two patients from family B and 16 cm and 1.2 cm in the two patients from family C. Expression of phosphorylated-mechanistic target of rapamycin was determined in the TSC-RAML tissues by immunohistochemistry. The maximum diameter of the tumor decreased by 4.90 and 5.30 cm, respectively, in the 2 patients treated with everolimus after 3 months. In conclusion, TSC cannot be easily diagnosed due to its variable characteristics. Growth of TSC-RAML may increase the bleeding risk and reduce the level of hemoglobin, but it does not greatly affect renal function. Individual differences in tumor dimensions existed even with the same pathogenic mutation, except for cases of coexistent non-pathogenic mutations. Everolimus treatment appears to be able to significantly reduce the size of TSC-RAML.
结节性硬化症相关肾血管平滑肌脂肪瘤(TSC-RAML)具有较高的出血风险甚至死亡风险。然而,关于中国家系中TSC-RAML的数据极其匮乏。本研究旨在通过获取6名先证者及其家庭成员的详细病史,并重新评估TSC-RAML患者进行的血液检查、计算机断层扫描和肾动态成像检查,来研究其临床和遗传特征。在2个家族中检测到TSC1/TSC2突变。共有3例TSC-RAML患者因出血风险高接受了部分肾切除术,另外2例接受了依维莫司治疗。其余6例TSC-RAML患者未接受临床干预,仅进行临床随访。结果发现,近37%(18/49)为TSC患者,6个家系的平均±标准差诊断年龄为34.22±17.73岁,其中61%(11/18)患有TSC-RAML。在11例TSC-RAML患者中,肿瘤最大直径在1.20至32.50 cm之间(平均±标准差,11.48±8.40 cm),单侧肾小球滤过率在27.20至60.10 ml/min之间(平均±标准差,42.55±9.73 ml/min),血清肌酐水平在40.00至90.00 µmol/l之间(平均±标准差,64.84±16.15 µmol/l),血红蛋白浓度在76.00至140.00 g/l之间(平均±标准差,107.73±21.04 g/l)。分别在家族B和家族C中检测到TSC1(c.733C>T)和TSC2(c.788_789insC)的致病突变,以及某些非致病突变,家族B的2例患者中TSC-RAML的最大直径分别为0 cm和10.3 cm,家族C的2例患者中分别为16 cm和1.2 cm。通过免疫组织化学法测定TSC-RAML组织中磷酸化雷帕霉素作用靶点的表达。3个月后,2例接受依维莫司治疗的患者肿瘤最大直径分别缩小了4.90 cm和5.30 cm。总之,由于TSC特征多变,难以轻易诊断。TSC-RAML的生长可能增加出血风险并降低血红蛋白水平,但对肾功能影响不大。即使存在相同的致病突变,除了共存非致病突变的情况外,肿瘤大小也存在个体差异。依维莫司治疗似乎能够显著缩小TSC-RAML的大小。