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2.
Presse Med ; 28(2): 67-70, 1999 Jan 16.
Article in French | MEDLINE | ID: mdl-9989295

ABSTRACT

BACKGROUND: Side-effects, including autoimmune disorders, are frequent with D-penicillamine therapy. Proteinuria is observed in 10% of the patients, often secondary to extramembranous glomerulopathy. Necrotizing extracapillary glomerulonephritis is however exceptional. CASE REPORTS: Two patients with systemic sclerodermia were treated with D-penicillamine for 7 and 14 years. Both developed necrotizing extracapillary glomerulonephritis with anti-myeloperoxidase antibodies (anti-MPO), associated with hemorrhagic alveolitis in one case. Partial regression of the renal failure was obtained after withdrawal of D-penicillamine and combination treatment with prednisone and cyclophosphamide. DISCUSSION: Extracapillary glomerulonephritis or a lung-kidney syndrome are frequently associated with anti-MPO antineutrophil cytoplasm antibodies (ANCA). In systemic sclerodermia, the presence of anti-MPO appears to define a group of patients at risk of pauci-immune extracapillary glomerulonephritis or a lung-kidney syndrome. In addition, the presence of ANCA in patients with renal failure would suggest extracapillary glomerulonephritis rather than sclerodermic microangiopathy. Development of extracapillary glomerulonephritis with anti-MPO in patients who are taking D-penicillamine suggests that inductor mechanisms other than D-penicillamine are involved in the pathogenesis of these glomerulopathies.


Subject(s)
Glomerulonephritis/immunology , Penicillamine/therapeutic use , Raynaud Disease/complications , Scleroderma, Systemic/complications , Aged , Antibodies, Antineutrophil Cytoplasmic/immunology , Autoimmune Diseases/chemically induced , Female , Glomerulonephritis/chemically induced , Humans , Middle Aged , Penicillamine/adverse effects , Proteinuria/chemically induced , Raynaud Disease/immunology , Scleroderma, Systemic/drug therapy , Scleroderma, Systemic/immunology , Sex Factors
3.
Rev Pneumol Clin ; 54(5): 268-70, 1998 Oct.
Article in French | MEDLINE | ID: mdl-9894283

ABSTRACT

We report a case of acute respiratory distress with fatal outcome due to ictero-hemorrhagic leptospirosis. The association with an intra-alveolar hemorrhage suggested the corticosteroid therapy would be useful in this case.


Subject(s)
Respiratory Distress Syndrome/etiology , Weil Disease/complications , Acute Disease , Adult , Humans , Infant, Newborn , Male , Radiography, Thoracic , Respiratory Distress Syndrome/diagnosis , Respiratory Distress Syndrome/diagnostic imaging , Weil Disease/diagnosis
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