Giant Lymphadenopathy Infiltrated by Gaucher Cells Mimicking Lymphoma


Yagci B., Salor O. , YALÇIN B. , Guerakan F., Guecer S., Bueyuepamukcu M.

PEDIATRIC BLOOD & CANCER, cilt.52, ss.870-871, 2009 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 52 Konu: 7
  • Basım Tarihi: 2009
  • Doi Numarası: 10.1002/pbc.21948
  • Dergi Adı: PEDIATRIC BLOOD & CANCER
  • Sayfa Sayıları: ss.870-871

Özet

Gaucher disease (GD) is a lysosomal storage disease characterized by deficiency of beta-glucocerebrosidase, which results in accumulation of glucocerebroside in reticuloendothelial system, bone marrow infiltration, progressive hepatosplenomegaly, and skeletal complications. Herein we report a 5-year-old female with GD receiving enzyme replacement therapy who had giant mesenteric lymphadenopathies. Pediatr Blood Cancer 2009;52:870-871. (C) 2009 Wiley-Liss, Inc.