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青紫型肾病——形态计量学分析

Cyanotic nephropathy--a morphometric analysis.

作者信息

Gupte Prajakta A, Vaideeswar Pradeep, Kandalkar Bhuvaneshwari M

机构信息

Department of Pathology (Cardiovascular & Thoracic Division), Seth GS Medical College, Mumbai, India.

出版信息

Congenit Heart Dis. 2014 Jul-Aug;9(4):280-5. doi: 10.1111/chd.12121. Epub 2013 Jul 9.

Abstract

OBJECTIVE

Nephropathy is a known complication in cyanotic congenital heart disease (CCHD). This study was undertaken for an objective analysis of histopathological changes of cyanotic nephropathy at autopsy.

DESIGN

Retrospective case records studied.

SETTING

Tertiary care teaching hospital affiliated to medical college in Mumbai, India.

PATIENTS AND METHODS

The renal histopathological findings of 50 consecutive autopsies in patients with CCHD were compared with 25 age-matched controls. The Bowman's capsular, glomerular tuft, and hilar arteriolar diameters were measured morphometrically. Statistical analysis was performed using unpaired t-test. A P value equal to or less than .05 was considered significant.

RESULTS

Among the 50 autopsied cases of CCHD, there were 35 males and 15 females, with a mean age of 4.64 years. The renal changes observed were glomerulomegaly, glomerulosclerosis, periglomerular fibrosis, hyperplastic arteriolosclerosis, and interstitial fibrosis. The objectively measured parameters were higher in cases as compared with controls in all age groups, and further these were also found to be higher in patients having decreased pulmonary arterial blood flow than those having normal to increased pulmonary arterial blood flow. The difference in Bowman's capsular and glomerular tuft diameters was statistically significant in the neonates and children in the age groups, 1-5 years and above 10 years. The difference in hilar arteriolar diameter was statistically significant for all age groups except neonates.

CONCLUSION

Patients with CCHD show significant changes in the kidneys as assessed morphometrically, leading to renal dysfunction, and the age of the patients plays a role in their development.

摘要

目的

肾病是已知的青紫型先天性心脏病(CCHD)并发症。本研究旨在对尸检时青紫型肾病的组织病理学变化进行客观分析。

设计

回顾性病例记录研究。

地点

印度孟买一所医学院附属的三级医疗教学医院。

患者和方法

将50例连续尸检的CCHD患者的肾脏组织病理学结果与25例年龄匹配的对照进行比较。采用形态测量法测量鲍曼囊、肾小球簇和肾门小动脉直径。使用非配对t检验进行统计分析。P值等于或小于0.05被认为具有统计学意义。

结果

在50例CCHD尸检病例中,男性35例,女性15例,平均年龄4.64岁。观察到的肾脏变化包括肾小球肿大、肾小球硬化、肾小球周围纤维化、增生性小动脉硬化和间质纤维化。在所有年龄组中,病例的客观测量参数均高于对照组,而且还发现肺动脉血流减少的患者高于肺动脉血流正常至增加的患者。在1至5岁和10岁以上年龄组的新生儿和儿童中,鲍曼囊和肾小球簇直径的差异具有统计学意义。除新生儿外,所有年龄组的肾门小动脉直径差异均具有统计学意义。

结论

经形态测量评估,CCHD患者的肾脏有显著变化,导致肾功能障碍,且患者年龄在这些变化的发展中起作用。

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