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Generalized lymphadenopathy as an initial presentation of systemic lupus erythematosus: case report and review of the literature.
- Source :
- Egyptian Rheumatology & Rehabilitation; 8/6/2024, Vol. 51 Issue 1, p1-7, 7p
- Publication Year :
- 2024
-
Abstract
- Background: Systemic lupus erythematosus (SLE) is a chronic multisystemic autoimmune disorder with a wide array of clinical manifestations. Lymphadenopathy is occasionally observed in patients with SLE, and although it is sometimes a feature of active disease, it is rarely the initial presenting feature at the time of diagnosis. Case presentation: We report the case of a 35-year-old woman with clinical features of generalized lymphadenopathy, fatigue, fever, and malaise of approximately 3 months duration with no other constitutional disorders or systemic involvement suggestive of SLE. Despite extensive laboratory, radiological, and histological evaluations for malignancies and infectious causes of generalized lymphadenopathy, all results returned normal. About a month later, she developed inflammatory polyarthritis, with a markedly elevated erythrocyte sedimentation rate (ESR) of 120 mm/h, and a subsequent serologic workup confirmed the diagnosis of SLE. Autoimmune serology testing revealed positive results for various antibodies, including antinuclear antibody (ANA) at a titre of 1:5120, homogenous and speckled pattern, anti-Sm, anti-dsDNA, U1-snRNP, Ku, SSA-AntiRo, SSB-AntiLa, anti-SM/RNP, anti-Histone, ribosomal-p protein, and anti-nucleosome antibodies. The diagnosis of SLE was established using the 2019 European League Against Rheumatism/American College of Rheumatology (EULAR/ ACR) criteria. She was on oral prednisolone, hydroxychloroquine, and calcium/vitamin D3 tablets. The patient improved remarkably, all swollen lymph nodes regressed spontaneously and she had no further need for a hematology review. Conclusion: While similar cases have been reported in Europe and some parts of Asia, in Africa, a careful search of the literature revealed that such cases have been reported only from Egypt in North Africa and not from other parts of the continent; hence, this case report highlights the importance of recognizing atypical presentations of SLE to improve awareness and diagnosis in different regions. [ABSTRACT FROM AUTHOR]
- Subjects :
- SYSTEMIC lupus erythematosus diagnosis
AUTOIMMUNE disease diagnosis
HYDROXYCHLOROQUINE
BLOOD testing
DIFFERENTIAL diagnosis
IMMUNOGLOBULIN G
FATIGUE (Physiology)
RARE diseases
SEX distribution
COMPUTED tomography
SYSTEMIC lupus erythematosus
FEVER
BLOOD sedimentation
FLUORESCENT antibody technique
PREDNISOLONE
POPULATION geography
CALCIUM
CHOLECALCIFEROL
ARTHRITIS
LITERATURE reviews
LYMPHATIC diseases
SYMPTOMS
Subjects
Details
- Language :
- English
- ISSN :
- 1110161X
- Volume :
- 51
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Egyptian Rheumatology & Rehabilitation
- Publication Type :
- Academic Journal
- Accession number :
- 178855071
- Full Text :
- https://doi.org/10.1186/s43166-024-00274-5