期刊文献+

伴食管及胃巨大平滑肌瘤Alport综合征的影像学特征 被引量:3

Imaging features of Alport syndrome combined with huge esophageal and gastric leiomyoma
原文传递
导出
摘要 Alport综合征是遗传性肾小球基底膜疾病,血尿、感音神经性耳聋及进行性肾功能减退是主要临床症状,可伴有眼部异常,此外极少数患者伴有弥漫性平滑肌瘤.Alport综合征伴弥漫性平滑肌瘤发生率低,受累部位常为食管、气管和女性生殖道等,并可出现吞咽困难、餐后呕吐,反复发作性支气管炎等呼吸困难的症状,其中以弥漫性食管平滑肌瘤最常见.同时伴有食管及胃巨大平滑肌瘤的Alport综合征的患者罕见,通过分析临床资料,总结该病的影像学表现,旨在提高对该病的认识及诊断水平. Alport syndrome is a hereditary glomerular basement membrane disease.Hematuria,sensorineural deafness and progressive renal function impairment is the main clinical symptoms.Alport syndrome can be associated with ocular abnormalities,and a few of patients were complicated with diffuse leiomyoma.The incidence of Alport syndrome with diffuse leiomyoma is low,and it mainly invades esophagus,the trachea and female genital tract,et al.Patients with Alport syndrome and diffuse leiomyoma have difficulty in swallowing and postprandial vomiting,recurrent bronchitis symptoms and dyspnea.Diffuse leiomyoma is commonly seen in the esophagus.Alport syndrome with huge esophageal and gastric leiomyoma is rarely seen in clinical practice.In this article,the imaging manifestations of Alport syndrome combined with huge esophageal and gastric leiomyoma is summarized to improve the understanding and diagnostic accuracy of this disease.
出处 《中华消化外科杂志》 CAS CSCD 北大核心 2014年第9期730-733,共4页 Chinese Journal of Digestive Surgery
关键词 ALPORT综合征 食管平滑肌瘤 胃平滑肌瘤 影像学诊断 Alport syndrome Esophageal leiomyoma Gastric Leiomyoma Imageological diagnosis
  • 相关文献

参考文献5

二级参考文献43

  • 1杨霁云,刘景诚.我国小儿肾小球疾病肾组织病理改变(2315例肾活检材料的综合分析)[J].中华儿科杂志,1996,34(5):319-323. 被引量:43
  • 2丁洁,杨霁云,刘景城,俞礼霞.免疫荧光学方法检查皮肤组织Ⅳ型胶原α5链诊断Alport综合征[J].中华儿科杂志,1997,35(4):177-179. 被引量:33
  • 3黎磊石,刘志红主编.中国肾脏病学[M].北京:人民军医出版社,2008,1328-1338
  • 4Wei G,Zhihong L,Huiping C,et al.Spectrum of clinical features and type Ⅳ collagen alpha-chain distribution in Chinese patients with Alport syndrome[J].Nephrol Dial Transplant,2006,21(11):3146-3154.
  • 5Kashtan CE. Familial hematuric syndromes-Alport syndrome, Thin glomerular basement membrane disease and Fechrner/Epstein syndromes. Contrib Nephrol. Basel, Karger,2001,136:pp79.
  • 6Pirson Y. Making the diagnosis of Alport's syndrome. Kidney Int, 1999, 56:760.
  • 7Jais JP, Knebelmann B, Giatms I, et al. X-linked Alport syndrome: Natural history in 195 families and genotype-phentotype correlations in males. J Am Soc Nephrol, 2000, 11:649.
  • 8Pajari H, Setala K, Heiskari N, et al. Ocular findings in 34 patients with Alport syndrome: correlation of the rindings to mutations in COL4A5 gene. Acta Ophthalmol Scand, 1999, 77:214.
  • 9Antignae C, Heidet L. Mutations in Alport syndrome associated with diffuse esophageal leiomyomatosis. Contrib Nephrol. Basel, Kazger, 1996, 117:pp172.
  • 10Zhou J, Mochizuki T, Smeets H, et al. Deletion of the paired α5(Ⅳ) and α6( Ⅳ ) collagen genes in inherited smooth muscle tumors. Science, 1993, 261:1 167.

共引文献32

同被引文献10

引证文献3

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部