Unmasking lupus: Generalized lymphadenopathy mimicking lymphoma in Systemic Lupus Erythematosus: A case report and literature review

Lymphadenopathy can be the initial manifestation of Systemic Lupus Erythematosus (SLE). This can result in diagnostic challenges because of the overlap in presentation with other infective or malignant conditions. We present the case of a 25-year-old woman who presented with generalized lymphadenopathy and constitutional symptoms. Initial workup pointed towards a diagnosis of non-Hodgkin’s lymphoma. However, the findings on immunohistochemistry and the partial resolution of the lymphadenopathy following steroid therapy were inconsistent with a malignant aetiology. Ultimately, a diagnosis of SLE was confirmed after the patient developed features of nephrotic syndrome and cutaneous manifestations typical of SLE. The repeat lymph node biopsy and autoimmune workup further supported the diagnosis. This case highlights the importance of developing a comprehensive list of differential diagnoses and the need to consider autoimmune aetiologies for patients presenting with generalized lymphadenopathy as the primary symptom.

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Publication Details

Journal
Journal of Kenya Assocation of Physicians
Published
2025-09-16
DOI
https://doi.org/10.4314/jkap.v7i2.8
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
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article

Unmasking lupus: Generalized lymphadenopathy mimicking lymphoma in Systemic Lupus Erythematosus: A case report and literature review

S. Nakitare, E.K. Genga, Rita Githaiga
Journal of Kenya Assocation of Physicians
Autoimmune Bullous Skin Diseases
article

Unmasking lupus: Generalized lymphadenopathy mimicking lymphoma in Systemic Lupus Erythematosus: A case report and literature review

S. Nakitare, E.K. Genga, Rita Githaiga
article en

Abstract

Lymphadenopathy can be the initial manifestation of Systemic Lupus Erythematosus (SLE). This can result in diagnostic challenges because of the overlap in presentation with other infective or malignant conditions. We present the case of a 25-year-old woman who presented with generalized lymphadenopathy and constitutional symptoms. Initial workup pointed towards a diagnosis of non-Hodgkin’s lymphoma. However, the findings on immunohistochemistry and the partial resolution of the lymphadenopathy following steroid therapy were inconsistent with a malignant aetiology. Ultimately, a diagnosis of SLE was confirmed after the patient developed features of nephrotic syndrome and cutaneous manifestations typical of SLE. The repeat lymph node biopsy and autoimmune workup further supported the diagnosis. This case highlights the importance of developing a comprehensive list of differential diagnoses and the need to consider autoimmune aetiologies for patients presenting with generalized lymphadenopathy as the primary symptom.

Journal of Kenya Assocation of PhysiciansVol. 7(2)
Openalex Percentile: Top 64%
Autoimmune Bullous Skin Diseases
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