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.

引用

页码：38 / 41

页数：4

共 37 条

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