Case Report Systemic Lupus erythematosus SLE

Pradeepkumar Vyas (1) , Arunav Uchil (2) , Amara (3) , Abhishek (4) , Rahul (5) , Vidyadhara (6)
(1) a:1:{s:5:"en_US";s:45:"Holy Family Hospital Bandra west Mumbai India";} , India
(2) Sommaiya Hospital Mumbai , India
(3) , India
(4) Holy Family Hospital Bandra west Mumbai India , India
(5) Holy Family Hospital Bandra west Mumbai India , India
(6) , India

Abstract

Abstract: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can cause multi-organ involvement. Lupus nephritis is one of the most serious complications of SLE, affecting up to 60% of patients with SLE. While lupus nephritis is well known to clinicians, some pediatric cases may present with atypical symptoms, which can make it challenging to diagnose and manage. Hera we report a case a 12-year-old girl with an atypical presentation of lupus nephritis. She presented with fever, cough, vomiting, foamy urine, and swelling around her eyes. Lab results showed grade 3 renal impairment and positive ANA and anti-histone antibodies. A renal biopsy confirmed lupus nephritis. The patient was managed with hemodialysis and pulse steroids and cyclophosphamide, leading to significant improvement in her condition. We present a case report of a pediatric patient who presented with atypical symptoms of lupus nephritis, highlighting the diagnostic challenges and management strategies of this condition.CONCLUSION: In atypical Lupus nephritis the need for prompt diagnosis and appropriate management is essential to improve patient outcomes and prevent complications.

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Authors

Pradeepkumar Vyas
drvyaspradeep@gmail.com (Primary Contact)
Arunav Uchil
Amara
Abhishek
Rahul
Vidyadhara
Author Biography

Arunav Uchil, Sommaiya Hospital Mumbai

senior resident internal medicine 

Vyas, P., Uchil, A. U., Lobo, A., Shrikhande, A., Patil, R., & Lakkapan, V. (2024). Case Report: Systemic Lupus erythematosus SLE. Journal of Medical Case Reports and Reviews, 7(5). Retrieved from http://jmcrr.info/index.php/jmcrr/article/view/271
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