Oral Manifestations May Be the First Sign of Langerhans Cell Histiocytosis
Tarih
2013Yazar
Gencay, Koray
Sepet, Elif
Erdem, Arzu Pinar
Dervisoglu, Sergulen
Kasimoglu, Yelda
Sahin, Songul
Üst veri
Tüm öğe kaydını gösterÖzet
Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of histiocytes characterised by a proliferation of abnormal and clonal Langerhans cells. LCH most commonly occurs as a localised solitary bone lesion and appears predominantly in paediatric patients. This case resport presents clinicopathological features of this disorder in a 2-year-old boy.
Koleksiyonlar
- Makale [92796]