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Published on: November 1, 2015
A Practical Perspective of the Hematologic Manifestations of Systemic Lupus Erythematosus
Juan Camilo Santacruz1, Marta Juliana Mantilla1, Igor Rueda1
1Spondyloarthropathies Research Group, Universidad de La Sabana, Chía, COL.
Insights
Systemic lupus erythematosus (SLE) commonly involves hematologic issues like anemia and thrombocytopenia, often appearing early and persisting. Understanding these diverse blood-related symptoms is key for effective SLE diagnosis and treatment.
Area of Science:
- Rheumatology
- Hematology
- Internal Medicine
Background:
- Systemic lupus erythematosus (SLE) is a chronic, multisystem inflammatory disease of unknown etiology.
- Hematologic manifestations are common in SLE, often presenting early and impacting patient morbidity.
- These blood-related issues necessitate aggressive treatment with high-dose immunosuppressants.
Purpose of the Study:
- To comprehensively review the hematologic manifestations of SLE.
- To provide clinicians with a practical guide for diagnosing and treating these conditions.
- To highlight the diagnostic challenges, such as initial misclassification of conditions like hemolytic anemia and immune thrombocytopenia.
Main Methods:
- Literature review focusing on hematologic manifestations in SLE.
- Analysis of the spectrum of hematologic alterations in SLE patients.
- Discussion of diagnostic criteria and therapeutic approaches for SLE-related hematologic conditions.
Main Results:
- The spectrum of hematologic manifestations in SLE is broad, including lymphopenia, anemia, thrombocytopenia, and pancytopenia.
- Hematologic involvement often predominates in the early years of SLE and can be the initial presentation.
- Conditions like hemolytic anemia and immune thrombocytopenia may initially be misdiagnosed as idiopathic before being linked to SLE.
Conclusions:
- Hematologic manifestations are a significant feature of SLE, frequently indicating high disease activity.
- A multifactorial understanding of these alterations is crucial for comprehensive therapeutic strategies.
- This review aims to enhance clinical understanding and management of SLE-associated hematologic disorders.
Abstract:
Systemic lupus erythematosus (SLE) is a chronic inflammatory disease with an unknown etiology that can affect any organ or system of the human body. Hematological, renal, or central nervous system manifestations in these patients result in great morbidity because high doses of glucocorticoids, cytotoxic medications, or biological drugs are required to control these manifestations. It is noteworthy that hematological involvement predominates during the first years of the disease and tends to last over time, with the premise that it may be the initial manifestation of the disease. Clear examples of this are the cases of hemolytic anemia and immune thrombocytopenia that can be initially classified as idiopathic or primary to be later classified as secondary when associated with infections, medications, neoplasms, or autoimmune diseases. The spectrum of hematologic manifestations in SLE is very broad, including lymphopenia, anemia, thrombocytopenia, or pancytopenia. In some cases, lymphadenopathy and splenomegaly are also identified. The vast majority of these manifestations denote high disease activity. However, many of these alterations have a multifactorial cause that must be taken into account to adopt a more complete therapeutic approach. The objective of this review is to characterize in detail the hematological manifestations of SLE to offer clinicians a practical vision of its diagnosis and treatment.
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