Concomitant sickle cell disease and systemic lupus erythematosus: A single‐center case series

Sickle cell disease (SCD) and systemic lupus erythematosus (SLE) are two uncommon disorders each characterized by multisystemic manifestations. Individuals with SCD exhibit abnormalities in the complement pathway, which may predispose patients to develop autoimmune disorders such as SLE. As many man...

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Veröffentlicht in:Pediatric blood & cancer 2024-10, Vol.71 (10), p.e31194-n/a
Hauptverfasser: Lapite, Ajibike, Sánchez, Luisana M., Altaffer, Ana Luiza, Rae, Meredith, Ramirez, Andrea Ann, Muscal, Eyal, Yildirim‐Toruner, Cagri, Tubman, Venée N.
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container_end_page n/a
container_issue 10
container_start_page e31194
container_title Pediatric blood & cancer
container_volume 71
creator Lapite, Ajibike
Sánchez, Luisana M.
Altaffer, Ana Luiza
Rae, Meredith
Ramirez, Andrea Ann
Muscal, Eyal
Yildirim‐Toruner, Cagri
Tubman, Venée N.
description Sickle cell disease (SCD) and systemic lupus erythematosus (SLE) are two uncommon disorders each characterized by multisystemic manifestations. Individuals with SCD exhibit abnormalities in the complement pathway, which may predispose patients to develop autoimmune disorders such as SLE. As many manifestations of SLE mimic those of SCD, diagnosis and therapeutic management of SLE in a patient with known SCD may be delayed. In this study, we describe our institutional experience of diagnosing and managing concomitant SCD and SLE. We offer insights into the complex interplay between these conditions to enhance early recognition and effective management of concurrent SCD and SLE.
doi_str_mv 10.1002/pbc.31194
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source MEDLINE; Wiley Journals
subjects Adolescent
Anemia, Sickle Cell - complications
Autoimmune diseases
complement system
Disease management
Early experience
Female
Humans
Lupus Erythematosus, Systemic - complications
Sickle cell disease
Systemic lupus erythematosus
Young Adult
title Concomitant sickle cell disease and systemic lupus erythematosus: A single‐center case series
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