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类脂蛋白沉积症:印度病例综述。

Lipoid proteinosis: Review of Indian cases.

作者信息

Shah Jigna S, Shah Himali A

机构信息

Department of Oral Medicine and Radiology, Government Dental College and Hospital, Ahmedabad, Gujarat, India.

出版信息

J Oral Maxillofac Pathol. 2022 Apr-Jun;26(2):236-241. doi: 10.4103/jomfp.jomfp_249_21. Epub 2022 Jun 28.

Abstract

Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized by the deposition of amorphous hyaline material in the dermis and submucosal connective tissue. To date <500 cases of LP have been described and oral manifestations described in a very few reports. Indian cases are much less reported and reviewed. Hence, here review of 51 Indian LP cases along with a case of histologically proven LP in 12-year-old male patient with typical skin, ocular, laryngeal, oral and radiographic features is done. Cases from 1969 to 2021 were collected using keyword LP on google and google scholar and Indian cases were analyzed afterward. Review with case presentation regarding oral manifestations will help the oral physician to diagnose LP in early stage.

摘要

类脂蛋白沉积症(LP)是一种罕见的常染色体隐性疾病,其特征是无定形透明质物质沉积于真皮和黏膜下结缔组织。迄今为止,已报道的LP病例不足500例,仅有极少数报告描述了其口腔表现。印度的病例报告和综述则更少。因此,本文对51例印度LP病例进行了综述,并报告了1例12岁男性患者经组织学证实的LP病例,该患者具有典型的皮肤、眼部、喉部、口腔和影像学特征。通过在谷歌和谷歌学术上使用关键词LP收集了1969年至2021年的病例,随后对印度病例进行了分析。结合病例展示对口腔表现进行综述将有助于口腔医生早期诊断LP。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/9364649/e1b7a611f4c9/JOMFP-26-236-g001.jpg

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