Add to ORKGLangerhans cell histiocytosis (LCH) is a rare disorder affecting predominantly children and manifesting as bone pains, bony swellings and lytic lesions. Involvement of vertebrae as presenting manifestation is unusual. Here we have presented three cases of LCH, two of multifocal eosinophilic granuloma (MEG) and one of Hand Schuller Christian disease (HSC). One of the patients with MEG; had vertebral involvement as the presenting manifestation
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is an uncommon haematologi...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langerhans cell histiocytosis (LCH) represents a disorder characterised by an abnormal accumulation ...
Langerhans Cell Histiocytosis (LCH) is a disease of abnormal clonal proliferation of langerhans cell...
Langerhans cell histiocytosis (LCH) is a relatively rare disorder, accounting for less than 1 % of a...
International audienceLangerhans' cell histiocytosis (LCH) is a rare condition of children and young...
Background: Langerhans cell histiocytosis (LCH), typically found in children, is a rare single or mu...
Langerhans Cell Histiocytosis (LCH) is a rare granulomatous disease with an unknown origin. LCH occu...
Langerhans Cell Histiocytosis (LCH) is a rare disorder of the reticuloendothelial system associated ...
Langerhans cell histiocytosis (LCH) is a rare group of idiopathic diseases characterized by abnormal...
Langerhans cell histiocytosis (LCH) may clinically manifest in a variety of ways due to its ability ...
Langerhans cell histiocytosis (LCH) is a clonal histiocytic disorder. The variable clinical manifest...
Langerhans cell histiocytosis (LCH) is a rare group of idiopathic diseases characterized by abnormal...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is an uncommon haematologi...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langerhans cell histiocytosis (LCH) represents a disorder characterised by an abnormal accumulation ...
Langerhans Cell Histiocytosis (LCH) is a disease of abnormal clonal proliferation of langerhans cell...
Langerhans cell histiocytosis (LCH) is a relatively rare disorder, accounting for less than 1 % of a...
International audienceLangerhans' cell histiocytosis (LCH) is a rare condition of children and young...
Background: Langerhans cell histiocytosis (LCH), typically found in children, is a rare single or mu...
Langerhans Cell Histiocytosis (LCH) is a rare granulomatous disease with an unknown origin. LCH occu...
Langerhans Cell Histiocytosis (LCH) is a rare disorder of the reticuloendothelial system associated ...
Langerhans cell histiocytosis (LCH) is a rare group of idiopathic diseases characterized by abnormal...
Langerhans cell histiocytosis (LCH) may clinically manifest in a variety of ways due to its ability ...
Langerhans cell histiocytosis (LCH) is a clonal histiocytic disorder. The variable clinical manifest...
Langerhans cell histiocytosis (LCH) is a rare group of idiopathic diseases characterized by abnormal...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is an uncommon haematologi...
Langherans' cell histiocytosis (LCH) is a rare disease mostly affecting children in the first decade...