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丹吉尔病的病理学

Pathology of Tangier disease.

作者信息

Bale P M, Clifton-Bligh P, Benjamin B N, Whyte H M

出版信息

J Clin Pathol. 1971 Oct;24(7):609-16. doi: 10.1136/jcp.24.7.609.

Abstract

Two cases of Tangier disease are described in children from families unrelated to each other. Necropsy in one case, the first to be reported in this condition, showed large collections of cholesterol-laden macrophages in tonsils, thymus, lymph nodes, and colon, and moderate numbers in pyelonephritic scars and ureter. As the storage cells may be scanty in marrow, jejunum, and liver, the rectum is suggested as the site of choice for biopsy. The diagnosis was confirmed by demonstrating the absence of alpha-lipoproteins from the plasma of the living child, and by finding low plasma levels in both parents of both cases. The disease can be distinguished from other lipidoses by differences in the predominant sites of storage, staining reactions, and serum lipid studies.

摘要

本文描述了两例来自互不相关家庭的儿童丹吉尔病病例。其中一例进行了尸检,这是该病症首次报告的尸检病例,结果显示扁桃体、胸腺、淋巴结和结肠中有大量充满胆固醇的巨噬细胞,肾盂肾炎瘢痕和输尿管中也有中等数量的此类细胞。由于骨髓、空肠和肝脏中的储存细胞可能较少,建议将直肠作为活检的首选部位。通过证明患病儿童血浆中缺乏α脂蛋白,并发现两例患儿的父母血浆水平均较低,确诊了该疾病。该疾病可通过储存的主要部位差异、染色反应和血脂研究与其他脂质沉积症相区分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d5c/477105/4f28d933b2a5/jclinpath00096-0027-a.jpg

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