Collapsing glomerulonephritis with podocyte markers in hemophagocytic syndrome secondary to hepatosplenic T-cell lymphoma
The hemophagocytic syndrome is a serious clinical-histological entity secondary to different diseases. Collapsing glomerulonephritis is a proliferative podocytopathy that usually has an unfavorable renal prognosis. We present a case in which both entities were associated, which is an infrequent form...
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Veröffentlicht in: | Biomédica 2018-12, Vol.38 (4), p.456-462 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | spa |
Online-Zugang: | Volltext |
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Zusammenfassung: | The hemophagocytic syndrome is a serious clinical-histological entity secondary to different diseases. Collapsing glomerulonephritis is a proliferative podocytopathy that usually has an unfavorable renal prognosis. We present a case in which both entities were associated, which is an infrequent form of hepatosplenic T-cell lymphoma. In addition, we review the role of the markers of podocyte dedifferentiation in this glomerulopathy and its pathophysiology and treatment. |
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ISSN: | 0120-4157 |
DOI: | 10.7705/biomedica.v38i4.3893 |