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以多囊肾疾病为主要特征的3例成人先天性肝纤维化(作者译)。 3例

[Kidney polycystic disease as the major feature in three adults with congenital hepatic fibrosis. 3 cases (author's transl)].

作者信息

Dupond J L, Miguet J P, Carbillet J P, Saint Hillier Y, Perol C, Leconte des Floris R

出版信息

Nouv Presse Med. 1979 Sep 24;8(36):2885-8.

PMID:493094
Abstract

Congenital hepatic fibrosis is nearly always associated with ectasia of collecting tubules of the kidneys. This abnormality usually remains silent. In this study we report three cases of adult's CHF with associated renal failure treated by hemodialysis. In all three cases, renal injuries were indistinguishable from those found in adult-type of polycystic disease. The kidneys of our third patient, who underwent two nephrectomies at a 14-years interval, showed ectasia of the collecting tubules with only a few cortical cysts. The second one showed numerous large cysts and only a few ectatic tubules. Our data indicate that: renal failure can complicate the CHF course in adults. Uremia can be the pressenting feature; polycystic kidneys in CHF are microscopically different from those found in adult-type, they might be considered as the final stage in ectasia of collecting tubules.

摘要

先天性肝纤维化几乎总是与肾集合管扩张相关。这种异常通常没有症状。在本研究中,我们报告了3例接受血液透析治疗的成人先天性肝纤维化合并肾衰竭病例。在所有3例病例中,肾脏损伤与成人型多囊病的损伤难以区分。我们的第三位患者在14年间接受了两次肾切除术,其肾脏显示集合管扩张,仅有少数皮质囊肿。第二位患者有许多大囊肿,仅有少数扩张的肾小管。我们的数据表明:肾衰竭会使成人先天性肝纤维化的病程复杂化。尿毒症可能是其主要表现;先天性肝纤维化中的多囊肾在显微镜下与成人型不同,它们可能被视为集合管扩张的终末期。

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