• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Long term prognosis for babies with neonatal liver disease.新生儿肝病患儿的长期预后
Arch Dis Child. 1985 May;60(5):447-51. doi: 10.1136/adc.60.5.447.
2
Neonatal hepatitis: a follow-up study.新生儿肝炎:一项随访研究。
J Pediatr Gastroenterol Nutr. 1987 Mar-Apr;6(2):203-7. doi: 10.1097/00005176-198703000-00006.
3
Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract.肝内胆汁淤积且肝外胆道通畅的婴儿的长期预后
Arch Dis Child. 1981 May;56(5):373-6. doi: 10.1136/adc.56.5.373.
4
Studies of the aetiology of neonatal hepatitis and biliary atresia.新生儿肝炎和胆道闭锁的病因学研究。
Arch Dis Child. 1977 May;52(5):360-7. doi: 10.1136/adc.52.5.360.
5
Outcome of hepatobiliary scanning in neonatal hepatitis syndrome.新生儿肝炎综合征肝胆扫描的结果
J Nucl Med. 1997 Aug;38(8):1279-82.
6
Prognosis and life expectancy in chronic liver disease.慢性肝病的预后与预期寿命
Dig Dis Sci. 1995 Aug;40(8):1805-15. doi: 10.1007/BF02212706.
7
Hepatitis syndrome in infancy--an epidemiological survey with 10 year follow up.婴儿期肝炎综合征——一项为期10年随访的流行病学调查
Arch Dis Child. 1985 Jun;60(6):512-6. doi: 10.1136/adc.60.6.512.
8
Infantile cholestasis due to cytomegalovirus infection of the liver. A possible cause of paucity of interlobular bile ducts.肝脏巨细胞病毒感染所致婴儿胆汁淤积。小叶间胆管稀少的一个可能原因。
Arch Pathol Lab Med. 1993 Sep;117(9):942-4.
9
Cholestatic jaundice in infancy. The importance of familial and genetic factors in aetiology and prognosis.婴儿期胆汁淤积性黄疸。家族和遗传因素在病因及预后中的重要性。
Arch Dis Child. 1981 Aug;56(8):622-7. doi: 10.1136/adc.56.8.622.
10
Neonatal giant cell hepatitis: histological and etiological findings.新生儿巨细胞肝炎:组织学和病因学发现。
Am J Surg Pathol. 2010 Oct;34(10):1498-503. doi: 10.1097/PAS.0b013e3181f069ab.

引用本文的文献

1
Alpha-1-antitrypsin phenotypes in adult liver disease patients.成人肝病患者的α-1-抗胰蛋白酶表型。
Ups J Med Sci. 2009;114(4):228-34. doi: 10.3109/03009730903243472.
2
Hepatitis syndrome in infancy--an epidemiological survey with 10 year follow up.婴儿肝炎综合征——一项为期10年随访的流行病学调查
Arch Dis Child. 1985 Dec;60(12):1204. doi: 10.1136/adc.60.12.1204.
3
Ten minute radiopharmaceutical test in biliary atresia.胆道闭锁的十分钟放射性药物检查。
Arch Dis Child. 1987 Feb;62(2):180-4. doi: 10.1136/adc.62.2.180.

本文引用的文献

1
Cancer risk in ulcerative colitis: scientific requirements for the study of prognosis.溃疡性结肠炎的癌症风险:预后研究的科学要求
Gastroenterology. 1980 Jun;78(6):1632-5.
2
Cholestatic jaundice in infancy. The importance of familial and genetic factors in aetiology and prognosis.婴儿期胆汁淤积性黄疸。家族和遗传因素在病因及预后中的重要性。
Arch Dis Child. 1981 Aug;56(8):622-7. doi: 10.1136/adc.56.8.622.
3
Long-term prognosis for infants with intrahepatic cholestasis and patent extrahepatic biliary tract.肝内胆汁淤积且肝外胆道通畅的婴儿的长期预后
Arch Dis Child. 1981 May;56(5):373-6. doi: 10.1136/adc.56.5.373.
4
Bone disease in primary biliary cirrhosis: increased bone resorption and turnover in the absence of osteoporosis or osteomalacia.原发性胆汁性肝硬化中的骨病:在无骨质疏松或骨软化的情况下骨吸收和骨转换增加。
Hepatology. 1984 Jan-Feb;4(1):1-8. doi: 10.1002/hep.1840040101.
5
Early assessment of evolution of liver disease associated with alpha 1-antitrypsin deficiency in childhood.儿童α1-抗胰蛋白酶缺乏症相关肝病演变的早期评估。
J Pediatr. 1983 May;102(5):661-5. doi: 10.1016/s0022-3476(83)80230-3.
6
1 -Antitrypsin deficiency and neonatal hepatitis.α1-抗胰蛋白酶缺乏症与新生儿肝炎。
Br Med J. 1972 Aug 19;3(5824):435-9. doi: 10.1136/bmj.3.5824.435.
7
Long-term follow-up of neonatal hepatitis: safety and value of surgical exploration.新生儿肝炎的长期随访:手术探查的安全性及价值
Pediatrics. 1974 May;53(5):650-5.
8
Arteriohepatic dysplasia: familial pulmonary arterial stenosis with neonatal liver disease.动脉肝发育不良:伴有新生儿肝病的家族性肺动脉狭窄。
Arch Dis Child. 1973 Jun;48(6):459-66. doi: 10.1136/adc.48.6.459.
9
Neonatal cholestasis in alpha-1-antitrypsin deficient children. Clinical, genetic, histological and immunohistochemical findings.α-1抗胰蛋白酶缺乏儿童的新生儿胆汁淤积。临床、遗传、组织学和免疫组化研究结果。
Acta Paediatr Scand. 1972 Nov;61(6):632-42. doi: 10.1111/j.1651-2227.1972.tb15960.x.
10
Alpha 1 antitrypsinin the livers of patients with emphysema.
Science. 1972 Jan 7;175(4017):63-5. doi: 10.1126/science.175.4017.63.

新生儿肝病患儿的长期预后

Long term prognosis for babies with neonatal liver disease.

作者信息

Deutsch J, Smith A L, Danks D M, Campbell P E

出版信息

Arch Dis Child. 1985 May;60(5):447-51. doi: 10.1136/adc.60.5.447.

DOI:10.1136/adc.60.5.447
PMID:2990356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1777337/
Abstract

A total of 123 patients with neonatal liver disease without extrahepatic bile duct obstruction or arteriohepatic dysplasia have been studied for six to 18 years. Idiopathic neonatal hepatitis, present in 73 babies, carried a high mortality due to liver failure (18%), septicaemia (6%), and associated defects (14%), especially in the first year of life (25%). Progression to chronic liver disease in non-familial idiopathic cases occurred in three of 40 reviewed patients. Only 12 of these children were completely healthy, the remainder having other permanent disabilities (57%). Four of nine familial cases of idiopathic neonatal hepatitis died in the first 12 months of life as did two of the four reviewed survivors. Progression to chronic liver disease or to death was a continuous process without any interval of recovery in all but one of these patients. Among patients with a presumed infective cause, cytomegalovirus infection caused a particularly benign form of neonatal hepatitis but was a frequent cause of brain damage or other disabilities. Babies who survived other infective liver diseases showed complete healing of the liver damage. Neonatal liver disease associated with alpha 1 antitrypsin deficiency progressed to death or chronic liver disease in three of nine patients and was not associated with a paucity of interlobular bile ducts.

摘要

对123例无肝外胆管梗阻或动脉肝发育不良的新生儿肝病患者进行了6至18年的研究。73例婴儿患有特发性新生儿肝炎,因肝衰竭(18%)、败血症(6%)及相关缺陷(14%)导致的死亡率很高,尤其是在生命的第一年(25%)。在40例接受复查的非家族性特发性病例中,有3例进展为慢性肝病。这些儿童中只有12例完全健康,其余儿童有其他永久性残疾(57%)。9例家族性特发性新生儿肝炎病例中有4例在出生后的前12个月死亡,4例接受复查的幸存者中有2例也是如此。除1例患者外,所有这些患者进展为慢性肝病或死亡均为一个持续的过程,无任何恢复间隔。在推测有感染病因的患者中,巨细胞病毒感染导致一种特别良性的新生儿肝炎形式,但却是脑损伤或其他残疾的常见原因。在其他感染性肝病中存活下来的婴儿肝脏损伤完全愈合。与α1抗胰蛋白酶缺乏相关的新生儿肝病在9例患者中有3例进展为死亡或慢性肝病,且与小叶间胆管稀少无关。