Hemolytic uremic syndrome as a rare complication in a case of Castleman disease-Reference-Cited by-同舟云学术

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Hemolytic uremic syndrome as a rare complication in a case of Castleman disease

Published:2024-03-22 Issue:6 Volume:71 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Hsu Alexander D.¹^ORCID,Ricoy Giselle N.¹,Savell Van²,Becker Amy³,Nhlane Ndina⁴

Affiliation:

1. Department of Pediatrics Driscoll Children's Hospital Corpus Christi Texas USA

2. Department of Pediatric Pathology Driscoll Children's Hospital Corpus Christi Texas USA

3. Department of Pediatric Nephrology Driscoll Children's Hospital Corpus Christi Texas USA

4. Department of Pediatric Hematology and Oncology Driscoll Children's Hospital Corpus Christi Texas USA

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30969

Reference4 articles.

1. Clinicopathologic analysis of TAFRO syndrome demonstrates a distinct subtype of HHV-8-negative multicentric Castleman disease

2. Anti-interleukin-6 Receptor Antibody (Tocilizumab) Treatment of Multicentric Castleman's Disease

3. Association of vascular endothelial growth factor and renal thrombotic microangiopathy‐like lesions in patients with Castleman's disease

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