Langerhans' Cell Histiocytosis in Chest Wall / 대한흉부외과학회지
The Korean Journal of Thoracic and Cardiovascular Surgery
; : 506-510, 2001.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-152796
Biblioteca responsável:
WPRO
ABSTRACT
Langerhans' Cell Histiocytosis(LCH) is a disease of unknown origin, characterized by abnormal proliferation of Langerhans' cells. Previously, it has been called histiocytosis X, which included eosinophilic granuloma, Hand-Sch ller-Christian's disease, and Letterer-Siwe disease. Any organs or tissues such as skin, lymph nodes, bone and bone marrow can be involved. However, LCH of chest wall is rarely reported in our country. We experienced a 18 month old male child, who had osteolytic lesion involving the rib with axillary lymph node metastasis. The tumor was confirmed as LCH after surgery.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Costelas
/
Pele
/
Tórax
/
Medula Óssea
/
Histiocitose
/
Granuloma Eosinófilo
/
Histiocitose de Células de Langerhans
/
Parede Torácica
/
Linfonodos
/
Metástase Neoplásica
Limite:
Criança
/
Humanos
/
Lactente
/
Masculino
Idioma:
Coreano
Revista:
The Korean Journal of Thoracic and Cardiovascular Surgery
Ano de publicação:
2001
Tipo de documento:
Artigo