Three Cases with Langerhans Cell Histiocytosis with Sistemic Involvement [Sistemik Tutulum ile Giden Langerhans Hücreli Histiositozis'li Üç Vaka Sunumu]
Küçük Resim Yok
Tarih
2004
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Histiocytosis which is a proliferative process characterized by an accumulation of dentritic cells in various tissues and organs is a rare disease. It can occur as an isolated lesion or as widespread systemic disease involving virtually any body site. Langerhans cell histiocytosis was diagnosed by light microscopy in a 27-month-old boy and 16-month-old girl with anemia hepatosplenomegaly, exanthema and lesions on the skull and a 9-month-old girl with thymic and cutaneous involvement. Clinical and laboratory findings of the cases are discussed in the light of literature.
Açıklama
Anahtar Kelimeler
Childhood, Langerhans cell histiocytosis, Liver, Lung, Thymus
Kaynak
THOD - Turk Hematoloji-Onkoloji Dergisi
WoS Q Değeri
Scopus Q Değeri
N/A
Cilt
14
Sayı
1
