Giant lymphadenopathy infiltrated by gaucher cells mimicking lymphoma
Pediatric Blood and Cancer, cilt.52, sa.7, ss.870-871, 2009 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 52 Sayı: 7
- Basım Tarihi: 2009
- Doi Numarası: 10.1002/pbc.21948
- Dergi Adı: Pediatric Blood and Cancer
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.870-871
- Anahtar Kelimeler: abdominal mass, enzyme replacement therapy, Gaucher disease, lymphoma
- Sağlık Bilimleri Üniversitesi Adresli: Evet
Özet
Gaucher disease (GD) is a lysosomal storage disease characterized by deficiency of b-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. © 2009 Wiley-Liss, Inc.