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慢性非神经型尼曼-匹克病患者的海蓝组织细胞增生症

Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick disease.

作者信息

Dewhurst N, Besley G T, Finlayson N D, Parker A C

出版信息

J Clin Pathol. 1979 Nov;32(11):1121-7. doi: 10.1136/jcp.32.11.1121.

Abstract

A patient with Niemann-Pick disease is reported together with family studies. Her liver and bone marrow were shown to be infiltrated with sea blue histiocytes. Other organs, spleen and lung, were presumably also involved but histological proof was not obtained. Enzyme assay of leucocytes, lymphocytes, and cultured skin fibroblasts showed the patient to be deficient in sphingomyelinase activity. In fibroblasts, activity was 5% of normal while for the parents activity was about 50% of normal. The expected partial deficiency was not found using leucocytes or lymphocytes from the parents. Heat stability studies on fresh fibroblast extracts from the propositus indicated that residual sphingomyelinase activity was slightly more labile than that of the controls. It seems clear that chronic Niemann-Pick disease without neurological involvement is associated with sea blue histiocytosis.

摘要

本文报告了一例尼曼-匹克病患者及相关家系研究。其肝脏和骨髓可见海蓝色组织细胞浸润。推测脾脏和肺等其他器官也受累,但未获得组织学证据。对白细胞、淋巴细胞和培养的皮肤成纤维细胞进行酶分析显示,该患者鞘磷脂酶活性缺乏。在成纤维细胞中,活性仅为正常水平的5%,而其父母的活性约为正常水平的50%。使用父母的白细胞或淋巴细胞未发现预期的部分缺陷。对先证者新鲜成纤维细胞提取物进行的热稳定性研究表明,残留的鞘磷脂酶活性比对照组的活性稍不稳定。显然,无神经受累的慢性尼曼-匹克病与海蓝色组织细胞增生症相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b939/1145910/615c6f35e8a6/jclinpath00459-0048-a.jpg

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