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结节性硬化症患儿的肾脏病变生长

Renal lesion growth in children with tuberous sclerosis complex.

作者信息

Ewalt D H, Sheffield E, Sparagana S P, Delgado M R, Roach E S

机构信息

Department of Urology, University of Texas Southwestern Medical Center, Texas Scottish Rite Hospital for Children, Dallas, USA.

出版信息

J Urol. 1998 Jul;160(1):141-5.

PMID:9628635
Abstract

PURPOSE

Renal lesions, including angiomyolipoma, renal cysts (simple and polycystic kidney disease) and renal cell carcinoma, develop in patients with tuberous sclerosis complex. While there is limited information that these lesions may grow in adults with tuberous sclerosis complex, the incidence, characterization and growth rate in children have not been reported. Also, the age at which these lesions first appear, thus providing insight into their natural history, is unknown. We present our data from a longitudinal renal surveillance study of children with tuberous sclerosis complex.

MATERIALS AND METHODS

Since 1985 children with tuberous sclerosis complex at our hospital have undergone periodic renal imaging by ultrasonography or computerized tomography to monitor renal lesions. A total of 35 girls and 25 boys 1 to 18 years old have undergone at least 2 or more annual renal ultrasounds.

RESULTS

On initial evaluation 33 of 60 children (55%) (mean age 6.9 years) had an identifiable renal lesion, which increased to 48 of 60 (80%) at followup (mean age 10.5 years). Angiomyolipoma was the most frequent lesion (75%) followed by simple renal cysts (17%). Angiomyolipomas increased in size and/or number in 10 of 18 boys (56%) and 18 of 27 girls (66%). The largest growth rate in 1 year was from 0 to 4 cm. and from 5 to 9 cm. in diameter. The youngest patient demonstrated lesions at age 2 years. The average age at which a normal ultrasound became abnormal was 7.2 years. While a total of 27 patients had a normal ultrasound on entering the study, lesions had developed in 15 at followup (11 with angiomyolipomas, 4 with cysts). Five patients had cysts that had disappeared at followup. A 7-year-old boy had a 9 cm. renal cell carcinoma removed. One patient has renal lesions characteristic of autosomal dominant polycystic kidney disease.

CONCLUSIONS

Renal involvement in patients with tuberous sclerosis complex begins in infancy, and angiomyolipoma is the most common lesion (75%). Angiomyolipomas are more likely to grow than remain stable, although the rate of growth varies. Simple renal cysts may appear or disappear with time but angiomyolipomas do not disappear. An initially normal renal ultrasound does not rule out future development of lesions. Periodic surveillance is indicated in children with tuberous sclerosis complex.

摘要

目的

结节性硬化症患者会出现肾脏病变,包括肾血管平滑肌脂肪瘤、肾囊肿(单纯性和多囊性肾病)以及肾细胞癌。虽然关于这些病变在成年结节性硬化症患者中可能生长的信息有限,但儿童中的发病率、特征及生长速率尚未见报道。此外,这些病变首次出现的年龄,即对其自然病史的了解,也尚不清楚。我们展示了对结节性硬化症患儿进行的一项纵向肾脏监测研究的数据。

材料与方法

自1985年以来,我院的结节性硬化症患儿接受了定期肾脏超声或计算机断层扫描成像,以监测肾脏病变。共有35名女孩和25名男孩,年龄在1至18岁之间,接受了至少2次或更多次年度肾脏超声检查。

结果

在初始评估时,60名儿童中有33名(55%)(平均年龄6.9岁)有可识别的肾脏病变,随访时(平均年龄10.5岁)这一数字增至60名中的48名(80%)。肾血管平滑肌脂肪瘤是最常见的病变(75%),其次是单纯性肾囊肿(17%)。18名男孩中有10名(56%)和27名女孩中有18名(66%)的肾血管平滑肌脂肪瘤大小和/或数量增加。1年内最大生长速率为直径从0增至4厘米以及从5增至9厘米。最年幼的患者在2岁时出现病变。超声检查从正常变为异常的平均年龄为7.2岁。共有27名患者在进入研究时超声检查正常,但随访时有15名出现了病变(11名有肾血管平滑肌脂肪瘤,4名有囊肿)。5名患者的囊肿在随访时消失。一名7岁男孩切除了一个9厘米的肾细胞癌。一名患者有常染色体显性多囊肾病特征的肾脏病变。

结论

结节性硬化症患者的肾脏受累始于婴儿期,肾血管平滑肌脂肪瘤是最常见的病变(75%)。肾血管平滑肌脂肪瘤更有可能生长而非保持稳定,尽管生长速率有所不同。单纯性肾囊肿可能随时间出现或消失,但肾血管平滑肌脂肪瘤不会消失。最初肾脏超声检查正常并不能排除未来病变的发生。结节性硬化症患儿需要定期监测。

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