SYSTEMIC LUPUS ERYTHEMATOSUS ASSOCIATED WITH NEPHRITIC SYMPHROME IN AN INFANT PATIENT

SYSTEMIC LUPUS ERYTHEMATOSUS ASSOCIATED WITH NEPHRITIC SYMPHROME IN AN INFANT PATIENT

PIRES, CATARINA FERNANDES; LIMA, SIMONE SOARES; SOUSA, ROBERTA ORIANA ASSUNÇÃO LOPES; VALE, DÁRIO HENRIQUE ALVARENGA; GOMES, APARECIDA MAÍSA CARVALHO; CAMPOS, ANA TERESA SPÍNDOLA MADEIRA; MACÊDO, ANTÔNIO SILVA; OLIVEIRA, LUCAS AGUIAR ALENCAR; RÊGO, PEDRO VÍTOR LIMA

Pôster:

Systemic Lupus Erythematosus (SLE) is the prototypic autoimmune disease. It is characterized by multiple autoantibodies associated with multisystem illness. Pediatric lúpus has been estimated to account for 10% to 20% of all cases of SLS. The average age of onset is 12 years, with rare cases occurring at 5 years of age or younger. Diagnosis of Pediatric SLE occurs at a younger age in non-Caucasian populations.

Case report

1-year-and-1-month-old-girl, non caucasian, initially presented reduction in urinary volume (oliguria) associated with nausea and vomiting, which led the family to seek medical assistance. In the first moment, received treatment with gastrointestinal symptoms and water replacement in a primary care unit. During the treatment he presented hematuria and generalized edema, in addition to changes in pressure values. Due to this evolution, she was referred to a regional hospital, where was started a deeper investigation of the origin of the symptoms. At the time, the patient denied episodes of pharyngoamygdalitis or pyodermites, which spoke against acute diffuse glomerulonephritis (post-streptococcal). In addition, he presented urea of 98 mg/dl and creatinine of 0.99 mg/dl. Due to this fact, investigation was initiated for other probable causes of nephritic syndrome, and the following tests were ordered: cardiolipin IgG (negative result), cardiolipin IgM (indeterminate result), anti-MS (negative result), anti-ssa (RO) (negative result), anti-ssb (LA) (negative result), anca's "c", "p" and atypical (non-reagents), FAN (reagent), C3 and C4 (within normal values), anti-DNAn (non-reagent) and cardiolipin IgA (non-reagent). Due to the results of the exams and the clinical picture, SLE was suspected as an etiology, being initiated the treatment with prednisone 2mg/kg, diuretics and hydric restriction. At the same hospital hospitalization, renal biopsy was performed for better elucidation and characterization of the condition. The result of this study was secondary membranous nephropathy, with minimal tubulointerstitial repercussion, presence of large amounts of IgG and low amounts of IgA, IgM and C3 in MBG (highly suggestive result of lupidic nephritis grade V -MEMBRANE GLOMERULONEPHRITIS). Currently, the patient is undergoing treatment with pulse therapy (initially monthly and now quarterly) with 3 cycles of methylprednisolone and 1 of cyclophosphamide. Evolves with stabilization of the condition and good response to treatment, however, still follows with changes in renal function.

Conclusion

SLE is rare at 5 years of age or younger. especially with renal involvement which provides a higher degree of aggressiveness of the disease with catastrophic consequences to the patient.

Systemic Lupus Erythematosus (SLE) is the prototypic autoimmune disease. It is characterized by multiple autoantibodies associated with multisystem illness. Pediatric lúpus has been estimated to account for 10% to 20% of all cases of SLS. The average age of onset is 12 years, with rare cases occurring at 5 years of age or younger. Diagnosis of Pediatric SLE occurs at a younger age in non-Caucasian populations.

Case report

1-year-and-1-month-old-girl, non caucasian, initially presented reduction in urinary volume (oliguria) associated with nausea and vomiting, which led the family to seek medical assistance. In the first moment, received treatment with gastrointestinal symptoms and water replacement in a primary care unit. During the treatment he presented hematuria and generalized edema, in addition to changes in pressure values. Due to this evolution, she was referred to a regional hospital, where was started a deeper investigation of the origin of the symptoms. At the time, the patient denied episodes of pharyngoamygdalitis or pyodermites, which spoke against acute diffuse glomerulonephritis (post-streptococcal). In addition, he presented urea of 98 mg/dl and creatinine of 0.99 mg/dl. Due to this fact, investigation was initiated for other probable causes of nephritic syndrome, and the following tests were ordered: cardiolipin IgG (negative result), cardiolipin IgM (indeterminate result), anti-MS (negative result), anti-ssa (RO) (negative result), anti-ssb (LA) (negative result), anca's "c", "p" and atypical (non-reagents), FAN (reagent), C3 and C4 (within normal values), anti-DNAn (non-reagent) and cardiolipin IgA (non-reagent). Due to the results of the exams and the clinical picture, SLE was suspected as an etiology, being initiated the treatment with prednisone 2mg/kg, diuretics and hydric restriction. At the same hospital hospitalization, renal biopsy was performed for better elucidation and characterization of the condition. The result of this study was secondary membranous nephropathy, with minimal tubulointerstitial repercussion, presence of large amounts of IgG and low amounts of IgA, IgM and C3 in MBG (highly suggestive result of lupidic nephritis grade V -MEMBRANE GLOMERULONEPHRITIS). Currently, the patient is undergoing treatment with pulse therapy (initially monthly and now quarterly) with 3 cycles of methylprednisolone and 1 of cyclophosphamide. Evolves with stabilization of the condition and good response to treatment, however, still follows with changes in renal function.

Conclusion

SLE is rare at 5 years of age or younger. especially with renal involvement which provides a higher degree of aggressiveness of the disease with catastrophic consequences to the patient.

Palavras-chave:

DOI: 10.5151/sbr2019-268

Referências bibliográficas

• [1]

Como citar:

PIRES, CATARINA FERNANDES; LIMA, SIMONE SOARES; SOUSA, ROBERTA ORIANA ASSUNÇÃO LOPES; VALE, DÁRIO HENRIQUE ALVARENGA; GOMES, APARECIDA MAÍSA CARVALHO; CAMPOS, ANA TERESA SPÍNDOLA MADEIRA; MACÊDO, ANTÔNIO SILVA; OLIVEIRA, LUCAS AGUIAR ALENCAR; RÊGO, PEDRO VÍTOR LIMA; "SYSTEMIC LUPUS ERYTHEMATOSUS ASSOCIATED WITH NEPHRITIC SYMPHROME IN AN INFANT PATIENT", p-268-268. In: Anais do 36º Congresso Brasileiro de Reumatologia. [ISBN 978-85-212-1892-0]. São Paulo: Blucher, 2019.
ISSN 23577282, DOI 10.5151/sbr2019-268