Literature DB >> 29603588

Renal failure in pediatric Castleman disease: Four French cases with thrombotic microangiopathy.

Elie Cousin1, Hugues Flodrops2, Olivia Boyer3, Julien Hogan4, Mahe Ruin2, Anne Couderc4, Jean-Michel Goujon5, Sophie Taque1.   

Abstract

Pediatric Castleman disease (CD) is an uncommon and poorly understood disorder of the lymph nodes. Renal failure has not been described in pediatric multicentric CD (MCD). We report four cases, who presented with polyadenopathy, organomegaly, edema and fluid accumulations, high blood pressure, and acute renal failure. In all cases, renal biopsy confirmed diffuse thrombotic microangiopathy. Definitive diagnosis of MCD was made by a biopsy of an affected lymph node located by computer tomography before initiation of corticosteroid therapy. Treatment of CD with corticosteroid therapy and rituximab was rapidly effective without relapse to date.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  acute renal failure; pediatric Castleman disease; thrombotic microangiopathy

Mesh:

Year:  2018        PMID: 29603588     DOI: 10.1002/pbc.27045

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  1 in total

1.  Histologic and Laboratory Characteristics of Symptomatic and Asymptomatic Castleman Disease in the Pediatric Population.

Authors:  Karen M Chisholm; Mark D Fleming
Journal:  Am J Clin Pathol       Date:  2020-05-05       Impact factor: 2.493

  1 in total

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