系统性红斑狼疮伴嗜酸性粒细胞增多症一例罕见病例：病例报告及文献综述

An Unusual Case of Eosinophilia with Systemic Lupus Erythematosus: A Case Report and Review of Literature.

作者信息

Mishra Aman, Kuikel Sandip, Rauniyar Robin, Poudel Sagar, Thapa Sital, Pathak Nibesh, Rimal Suman, Pandey Kundan Raj, Jha Saket

机构信息

Maharajgunj Medical Campus, Tribhuvan University Institute of Medicine, Kathmandu, Maharajgunj 44600, Nepal.

Department of Internal Medicine, Tribhuvan University Institute of Medicine, Kathmandu, Maharajgunj 44600, Nepal.

出版信息

Case Rep Med. 2022 Feb 28;2022:3264002. doi: 10.1155/2022/3264002. eCollection 2022.

DOI:10.1155/2022/3264002

PMID:35265137

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8901357/

Abstract

Eosinophilia can be caused by various conditions, parasitic infection being the most common cause. Here, we present a case of a 17-year male who presented with multisystem involvement and eosinophilia. He was later diagnosed to have systemic lupus erythematosus with eosinophilia which is a rare combination. Despite being a diagnostic challenge, these patients can be well managed with immunosuppressive therapy if recognized in time.

摘要

嗜酸性粒细胞增多可由多种情况引起，其中寄生虫感染是最常见的原因。在此，我们报告一例17岁男性病例，该患者出现多系统受累及嗜酸性粒细胞增多。他后来被诊断为系统性红斑狼疮合并嗜酸性粒细胞增多，这是一种罕见的组合。尽管这是一个诊断难题，但如果能及时识别，这些患者可以通过免疫抑制治疗得到良好管理。