Collapsing glomerulonephritis with podocyte markers in hemophagocytic syndrome secondary to hepatosplenic T-cell lymphoma

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
Hauptverfasser: Martín-Gómez, María Adoración, Caba-Molina, Mercedes, Viciana-Martínez-Lage, María José, Ortega-Salas, Rosa, Sánchez-Crespo, Alicia, Soriano-Pérez, Manuel Jesús, Gómez-Morales, Mercedes
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container_issue 4
container_start_page 456
container_title Biomédica
container_volume 38
creator Martín-Gómez, María Adoración
Caba-Molina, Mercedes
Viciana-Martínez-Lage, María José
Ortega-Salas, Rosa
Sánchez-Crespo, Alicia
Soriano-Pérez, Manuel Jesús
Gómez-Morales, Mercedes
description 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.
doi_str_mv 10.7705/biomedica.v38i4.3893
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title Collapsing glomerulonephritis with podocyte markers in hemophagocytic syndrome secondary to hepatosplenic T-cell lymphoma
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