Literature DB >> 19533141

Diffuse proliferative glomerulonephritis associated with dermatomyositis with nephrotic syndrome.

Qibing Xie1, Yi Liu, Gang Liu, Nanping Yang, Geng Yin.   

Abstract

We described a 44-year-old man developing dermatomyositis (DM) and nephrotic syndrome (NS). Renal biopsy revealed diffuse proliferative glomerulonephritis (DPGN) with depositions of immunoglobulin and complements. A combination therapy of steroid and cyclophosphamide (CTX) was found very effective for the patient. Chronic glomerulonephritis is rare in DM. In our review of related literature, membranous glomerulonephritis (MN) is the main type of glomerular lesion, another type is mesangial proliferative glomerulonephritis (mesPGN). Here we reported a case of DM associated with DPGN developing NS, which was not found in existing literature. Although glomerulonephritis is uncommon in patients with DM, renal pathology is not as simplex as previously thought, and treatment with steroid or/and cytotoxic drugs is favorable for prognosis.

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Year:  2009        PMID: 19533141     DOI: 10.1007/s00296-009-1003-7

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  17 in total

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  7 in total

1.  Nephrotic syndrome and juvenile dermatomyositis.

Authors:  Azar Nickavar; Mitra Mehr Azma
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7.  The spectrum of renal involvement in patients with inflammatory myopathies.

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Journal:  Medicine (Baltimore)       Date:  2014-01       Impact factor: 1.889

  7 in total

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