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Systemic lupus erythematosus mimicking idiopathic multicentric Castleman disease: A diagnostic dilemma
Kuis Gunathilake1, Mim Rifath2, B M Munasinghe1
1Postgraduate Institute of Medicine, University of Colombo, Colombo, Sri Lanka.
Insights
Castleman disease can mimic autoimmune disorders like systemic lupus erythematosus (SLE), posing diagnostic challenges. This case highlights a patient initially diagnosed with Castleman disease who later met SLE criteria, responding well to SLE treatment.
Area of Science:
- Immunology
- Rheumatology
- Hematology
Background:
- Castleman disease is a rare lymphoproliferative disorder that can present with diverse clinical manifestations.
- It often mimics other conditions, including autoimmune diseases and malignancies, complicating diagnosis.
- Systemic lupus erythematosus (SLE) shares overlapping clinical and laboratory features with Castleman disease, creating a diagnostic challenge.
Observation:
- A young female patient initially presented with symptoms suggestive of idiopathic multicentric Castleman disease.
- Subsequently, she developed antinuclear antibody (ANA) positivity and met the diagnostic criteria for SLE.
- This presentation underscores the diagnostic complexity when these two conditions overlap.
Findings:
- The patient's initial presentation mimicked Castleman disease, but the subsequent development of ANA positivity indicated SLE.
- Treatment initiated for systemic lupus erythematosus led to a significant clinical and biochemical improvement.
- This suggests that in certain overlapping cases, SLE treatment may be effective.
Implications:
- This case highlights the importance of considering SLE in patients with Castleman disease-like symptoms, especially with serological evidence.
- Accurate differentiation and timely diagnosis are crucial for effective management of these overlapping conditions.
- Further research may elucidate sharedpathogenic mechanisms between Castleman disease and SLE.
Abstract:
Castleman disease is a heterogeneous group of disorders of lymphoid tissue. It can often mimic other autoimmune diseases or malignancies, presenting a diagnostic dilemma to attending clinicians. Systemic lupus erythematosus and Castleman disease share many clinical and biochemical features rendering a special diagnostic challenge. Herein, we report a case of a young female who initially presented with features of idiopathic multicentric Castleman disease, subsequently developed antinuclear antibody positivity, and fulfilled the criteria for the diagnosis of systemic lupus erythematosus. Following the commencement of treatment for systemic lupus erythematosus, she had a marked response with resolution of altered clinical and biochemical profile.
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