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Warm Autoimmune Hemolytic Anemia as the Initial Presentation of Systemic Lupus Erythematosus (SLE): A Case Report

Patient: Female, 32-year-old Final Diagnosis: Anemia • hemolytic anemia • systemic lupus erythematosus Symptoms: Fatigue • weakness Medication: — Clinical Procedure: — Specialty: Hematology • Immunology OBJECTIVE: Unknown etiology BACKGROUND: Autoimmune hemolytic anemia is an acquired disorder resul...

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Detalles Bibliográficos
Autores principales: Kander, Tejaswi, Kim, Jinah, Gomez, Janet Chan, Joseph, Maria, Bhandari, Binita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8672920/
https://www.ncbi.nlm.nih.gov/pubmed/34897265
http://dx.doi.org/10.12659/AJCR.932965
Descripción
Sumario:Patient: Female, 32-year-old Final Diagnosis: Anemia • hemolytic anemia • systemic lupus erythematosus Symptoms: Fatigue • weakness Medication: — Clinical Procedure: — Specialty: Hematology • Immunology OBJECTIVE: Unknown etiology BACKGROUND: Autoimmune hemolytic anemia is an acquired disorder resulting in the presence of antibodies against red blood cell (RBC) antigens causing hemolysis. Autoimmune hemolytic anemia is of 2 types, Warm antibody mediated and cold agglutinin disease. Warm autoimmune hemolytic anemia (warm agglutinin disease) usually presents with fatigue and other constitutional symptoms and is diagnosed by the presence of IgG antibodies. The disease can occur as idiopathic or secondary to other autoimmune diseases, infections, or even malignancies. The systemic lupus erythematosus (SLE) is an autoimmune disease prevalent in young females. Autoimmune hemolytic anemia can occur as a part of the SLE spectrum however warm autoimmune hemolytic anemia as the initial manifestation of SLE is extremely rare. CASE REPORT: Here, we describe a unique case of a 32-year-old woman who presented with vague clinical presentation found to have warm autoimmune hemolytic anemia and further immunological and inflammatory work-up during and after hospitalization lead to the diagnosis of systemic lupus erythematosus. CONCLUSIONS: The systemic lupus erythematosus (SLE) is an autoimmune chronic inflammatory disease with unclear etiology affecting multi organs. Variable presentation in addition to the lack of definite pathognomonic features or tests makes the diagnosis of SLE challenging. On the whole autoimmune hemolytic anemia can not only be part of other disease processes but can be an initial presentation, highlighting the importance of thorough work-up in patients presenting with autoimmune hemolytic anemia to aid in timely diagnosis and management of underlying secondary conditions. It is important for providers to be aware of various disease spectrums that contain autoimmune hemolytic anemia for day-to-day clinical practice.