SciELO - Scientific Electronic Library Online

 
vol.38 issue4X-linked epileptic syndrome by protocadherin 19 mutation associated with leukoencephalopathy and posterior reversible tractopathy author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars 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.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )