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

Author:

Chisholm Karen M12,Fleming Mark D3

Affiliation:

1. Department of Laboratories, Seattle Children’s Hospital, Seattle, WA

2. Department of Laboratory Medicine, University of Washington, Seattle

3. Department of Pathology, Boston Children’s Hospital, Boston, MA

Abstract

Abstract Objectives Compare the morphologic, laboratory, and clinical features of asymptomatic and symptomatic Castleman disease in the pediatric population. Methods We reviewed clinical records and histopathology of patients with Castleman disease from 2 pediatric institutions. Results Of 39 patients with pediatric Castleman disease, 37 had unicentric disease, all classified with the hyaline vascular variant of Castleman disease, 8 of which were clinically symptomatic. These 8 patients demonstrated abnormal laboratory findings, including microcytic anemia, elevated erythrocyte sedimentation rate and C-reactive protein, and hypoalbuminemia. In addition, histopathologic evaluation showed that the 8 symptomatic cases had more hyperplastic germinal centers, fewer atrophic or regressed germinal centers, fewer mantle zones containing multiple germinal centers, reduced “onion skinning” of mantle zones, and fewer “lollipop” formations compared with the asymptomatic cases. Conclusions This series of pediatric Castleman disease showed that lymph nodes from asymptomatic patients generally demonstrated the more classic hyaline vascular histology, whereas those with symptoms could lack or have only focal classic findings. As such, reactive lymph nodes with subtle Castleman-like features should prompt clinical correlation to ensure proper diagnosis.

Funder

Seattle Children’s Mark Alan Bomgardner Endowment

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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