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伴有髓质海绵肾的先天性肝纤维化一例 被引量:1

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摘要 患者男,18岁.因"间断呕血、黑便12 d"收住大连医科大学附属第一医院消化科.入院体检:贫血貌,巩膜无黄染,无肝掌、蜘蛛痣,双肺呼吸音清,未闻及干湿性哕音;心率86次/min,心律齐,未闻及杂音;腹平软,腹壁可见静脉曲张,肝肋下3 cm,脾肋下6 cm,移动性浊音(-);双下肢无水肿.
出处 《中华内科杂志》 CAS CSCD 北大核心 2010年第12期1060-1061,共2页 Chinese Journal of Internal Medicine
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同被引文献7

  • 1Kerr DN, Harrison CV, Sherlock S, et al. Congenital hepatic fi- brosis. Q J Med,1961,30 :91-117.
  • 2Johnson CA, Gissen P, Sergi C. Molecular pathology and genetics ofcongenial hepatorenal fibrocystic syndromes. J Med Genet, 2003,40(5 ) :311-319.
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  • 4Zeitoun D, Brancatelli G, Colombat M, et al. Congenital hepatic fibrosis : CT findings in 18 adults. Radiology ,2004,231 ( 1 ) : 109- 116.
  • 5Rossi S, Assis DN, Awsare M, et al. Use of over-the-counter an- algesics in patients with chronic liver disease: physicians ' recom- mendations. Drug Saf,2008,31 ( 3 ) :261-270.
  • 6赵新颜,张新,王泰龄,欧晓娟,贾继东.先天性肝纤维化14例临床病理特点[J].临床肝胆病杂志,2010,26(2):191-193. 被引量:9
  • 7张伟,高俊茹,郎艳华,邵乐平.成人常染色体显性遗传性多囊肾并发先天性肝纤维化一例[J].中华肾脏病杂志,2011,27(7):547-547. 被引量:2

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