Nephrotic syndrome and arthritis in a 12-year-old girl.

NEPHROTIC SYNDROME (NS) in a 12year-old girl may present a diagnostic problem concerning the underlying disease. NS in childhood may be primary or secondary. In childhood, the main cause of NS is minimal change disease. The peak age of minimal change disease is between the ages of 2 and 7 years.1 At 12 years of age, the incidence of idiopathic nephrotic syndrome has started to decrease. NS at this age may be attributable to other primary renal diseases, or it can be secondary to a rheumatic disease such as lupus, or secondary to an infection or malignancy. If there are accompanying extrarenal features such as arthritis and rash, the differential diagnosis also includes vasculitis. Other unusual causes of NS, such as secondary (AA-type) amyloidosis, are more common in certain geographic areas and ethnic groups. Secondary amyloidosis can be associated with juvenile idiopathic arthritis, familial Mediterranean fever, or chronic suppurative infections. A renal biopsy to establish the diagnosis is indicated if the child’s condition is resistant to steroid treatment.

[1]  A. Bakkaloğlu,et al.  Renal involvement in polyarteritis nodosa: evaluation of 26 Turkish children , 2000, Pediatric Nephrology.

[2]  S. Ozen Vasculopathy, Behçet's syndrome, and familial Mediterranean fever. , 1999, Current opinion in rheumatology.

[3]  M. Suarez‐Almazor,et al.  Revision of the proposed classification criteria for juvenile idiopathic arthritis: Durban, 1997. , 1998, The Journal of rheumatology.

[4]  D. Kastner,et al.  Familial Mediterranean fever at the millennium. Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health. , 1998, Medicine.

[5]  E. Ben-Chetrit,et al.  Familial Mediterranean fever , 1998, The Lancet.

[6]  D. Zemer,et al.  Criteria for the diagnosis of familial Mediterranean fever. , 1997, Arthritis and rheumatism.

[7]  A. Bakkaloğlu,et al.  Familial Mediterranean fever and polyarteritis nodosa: experience of five paediatric cases. A causal relationship or coincidence? , 1997, European journal of pediatrics.

[8]  N. Tuzuner,et al.  Vasculitis in familial Mediterranean fever. , 1997, The Journal of rheumatology.

[9]  D. Zemer,et al.  The changing face of familial Mediterranean fever. , 1996, Seminars in arthritis and rheumatism.

[10]  K. Tınaztepe Renal amyloidosis in childhood. An overview of the topic with 25 years experience. , 1995, Turkish Journal of Pediatrics.

[11]  A. Bakkaloğlu,et al.  Familial Mediterranean fever and amyloidosis in children , 1993, Acta paediatrica.

[12]  M. Korppi,et al.  RNA hybridization for Mycoplasma pneumoniae: a new tool for following the epidemiological situation , 1992, Acta paediatrica.