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Clinical and pathological characteristics of Castleman disease: an observational study in a Spanish tertiary hospital.

Andrés González GarcíaJosé Luis Patier de la PeñaMónica García-CosioYasmina SarhaneCristina Sánchez DíazIgnacio Barbolla DíazMónica López RodríguezMaría Ángeles MorenoJesús VillarubiaLuis Manzano
Published in: Leukemia & lymphoma (2019)
Castleman disease (CD) represents a heterogeneous group of lymphoproliferative disorders that share well-defined histopathological features. An observational study of patients with CD was conducted. A total of 53 patients had CD: 20 had the unicentric form (UCD) and 33 the multicentric (MCD) variant; 10 of the latter cases were infected with human herpesvirus-8 (HHV-8) and 23 were idiopathic (iMCD). Median age differed between UCD and iMCD (30 vs. 49 years, p = .004). Males were completely predominant in HHV-8-associated MCD (100%), and females were more frequent in UCD (75 vs. 48%, p = .06). Relapses were more frequent in iMCD (57 vs. 10% UCD, p = .002), and mortality was significantly higher in iMCD and the HHV-8-associated form with respect to UCD. We conclude that UCD is a benign disorder of younger ages and female predominance, while iMCD represents a different entity with more disease relapses and higher mortality.
Keyphrases
  • end stage renal disease
  • cardiovascular events
  • ejection fraction
  • endothelial cells
  • risk factors
  • nk cells
  • epstein barr virus
  • peritoneal dialysis