Sickle cell disease and systematic lupus erythematous association in a 14-year-old adolescent female: A case report

被引：0
|
作者：
Safdar, Osama Y. [1 ]
Sindi, Sulafa Taher A. [1 ]
Nazer, Njood Waleed M. [1 ]
Azizkhan, Anan Zubair [1 ]
Alharbi, Noha Abdulkhalig [1 ]
机构：
[1] King Abdulaziz Univ Hosp, Paediat Dept, Jeddah, Saudi Arabia
来源：
AUSTRALASIAN MEDICAL JOURNAL | 2019年 / 12卷 / 01期
关键词：
SCD; SLE; Autoimmune; CHILDREN; ANEMIA;
D O I：
10.21767/AMJ.2018.3561
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
SCD develops when haemoglobin (HbS) is produced in the body as a result of a mutation occurring in haemoglobin beta chain. SLE is defined as a rare, chronic autoimmune multi-organ manifestation. SCD and SLE rarely coincide in literature due to the limited number of cases and the overlapping of symptoms of both diseases. Majority affecting child bearing age, with a mean of 23-year-old. Articular manifestations like joint pain are common in both diseases. We report a case of female adolescent with sickle cell disease associated with systemic lupus erythematous.
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收藏
页码：38 / 41
页数：4
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