Diagnostic pitfall: Castleman’s disease versus systemic lupus erythematosus in a woman with generalised lymphadenopathy

Systemic lupus erythematosus is an autoimmune disease with diverse systemic manifestations, while Castleman disease is a rare lymphoproliferative disorder that often presents with systemic symptoms and can mimic autoimmune disorders. β-thalassaemia trait is a genetic disorder characterised by mild anaemia. We report the case of a young female who presented with febrile episodes persisting for 6 months, accompanied by multiple joint pain and left-sided chest pain for 3 months. Physical examination revealed pallor, generalised lymphadenopathy, splenomegaly and left-sided pleural effusion. Lymph node biopsy initially suggested Castleman disease-hyaline vascular variant. However, further evaluation led to a final diagnosis of systemic lupus erythematosus with lupus nephritis and concomitant β-thalassaemia trait. This case highlights the diagnostic challenge when multiple diseases with overlapping symptoms coexist and the importance of a comprehensive evaluation in patients with atypical presentations to avoid diagnostic overshadowing.

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Publication Details

Journal
BMJ Case Reports
Published
2025-05-01
DOI
https://doi.org/10.1136/bcr-2024-264605
Citations
1
Primary Topic
Viral-associated cancers and disorders
Type
article
Field-Weighted Citation Impact
1.05
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article

Diagnostic pitfall: Castleman’s disease versus systemic lupus erythematosus in a woman with generalised lymphadenopathy

Chakrapani Mahabala, Shalini Radhakrishnan, Chaithra Gowthuvalli Venkataramana, Mohan Bhojraja Varadanayakanahalli
1 citations
BMJ Case Reports
Viral-associated cancers and disorders
1.05
article

Diagnostic pitfall: Castleman’s disease versus systemic lupus erythematosus in a woman with generalised lymphadenopathy

Chakrapani Mahabala, Shalini Radhakrishnan, Chaithra Gowthuvalli Venkataramana, Mohan Bhojraja Varadanayakanahalli
article en
1 citations

Abstract

Systemic lupus erythematosus is an autoimmune disease with diverse systemic manifestations, while Castleman disease is a rare lymphoproliferative disorder that often presents with systemic symptoms and can mimic autoimmune disorders. β-thalassaemia trait is a genetic disorder characterised by mild anaemia. We report the case of a young female who presented with febrile episodes persisting for 6 months, accompanied by multiple joint pain and left-sided chest pain for 3 months. Physical examination revealed pallor, generalised lymphadenopathy, splenomegaly and left-sided pleural effusion. Lymph node biopsy initially suggested Castleman disease-hyaline vascular variant. However, further evaluation led to a final diagnosis of systemic lupus erythematosus with lupus nephritis and concomitant β-thalassaemia trait. This case highlights the diagnostic challenge when multiple diseases with overlapping symptoms coexist and the importance of a comprehensive evaluation in patients with atypical presentations to avoid diagnostic overshadowing.

BMJ Case ReportsVol. 18(5)
Manipal Academy of Higher Education (IN), Kasturba Medical College, Manipal (IN)
Good health and well-being
Openalex Percentile: Top 22%
Viral-associated cancers and disorders
1.05
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