Services on Demand
Journal
Article
Indicators
- Cited by SciELO
- Access statistics
Related links
- Cited by Google
- Similars in SciELO
- Similars in Google
Share
Biomédica
Print version ISSN 0120-4157
Abstract
MARTIN-GOMEZ, María Adoración et al. Collapsing glomerulonephritis with podocyte markers in hemophagocytic syndrome secondary to hepatosplenic T-cell lymphoma. Biomédica [online]. 2018, vol.38, n.4, pp.456-462. ISSN 0120-4157. https://doi.org/10.7705/biomedica.v38i4.3893.
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.
Keywords : Glomerulonephritis; lymphohistiocytosis, hemophagocytic; lymphoma; renal insufficiency; antigens, differentitation; lymphoproliferative disorders.