| Literature DB >> 30653858 |
María Adoración Martín-Gómez1, Mercedes Caba-Molina, María José Viciana-Martínez-Lage, Rosa Ortega-Salas, Alicia Sánchez-Crespo, Manuel Jesús Soriano-Pérez, Mercedes Gómez-Morales.
Abstract
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.Entities:
Keywords: antígenos de diferenciación; glomerulonefritis; insuficiencia renal; linfohistiocitosis hemofagocítica; linfoma; trastornos linfoproliferativos
Mesh:
Year: 2018 PMID: 30653858 DOI: 10.7705/biomedica.v38i4.3893
Source DB: PubMed Journal: Biomedica ISSN: 0120-4157 Impact factor: 0.935