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Histiocitosis de células mixtas: reporte de un caso
(2022)
Introduction: Histiocytoses are rare diseases characterized by tissue infiltration by abnormal histiocytes. They are divided into five groups. They are frequent in the pediatric population. The combination of Langerhans ...
Symptomatic bone langerhans cell histiocytosis treated at diagnosis or after reactivation with indomethacin alone
(Lippincott Williams, 2014-07)
This study evaluated the outcome of patients with symptomatic bone Langerhans cell histiocytosis (LCH) treated with indomethacin alone, either at diagnosis or after reactivation (after recurrence with previous therapies). ...
Oral manifestations of histiocytosis of langerhans cells: a pediatric case involving mandible bone
(Facultad de Odontología. Universidad de Costa Rica, 2022)
Primary Rosai-Dorfman disease of boneEnfermedad de Rosai-Dorfman primaria ósea
(Universidad Nacional Mayor de San Marcos, Facultad de Medicina Humana, 2021)
Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood
(Wiley, 2014-12)
Skeletal involvement is generally, but not universally, characteristic of Langerhans cell histiocytosis (LCH). We investigated whether the presence of bone lesions at diagnosis is a prognostic factor for survival in LCH. ...
Histiocitosis de células de langerhans, granuloma eosinofílico de hueso temporal en adolescente. Caso Clínico
(Universidad del Norte, 2013)
High prevalence of BRAFV600E in patients with cholestasis, sclerosing cholangitis or liver fibrosis secondary to Langerhans cell histiocytosis
(Wiley-liss, div John Wiley & Sons Inc., 2021-07)
Targeted therapies with MAPK inhibitors have proven to modulate the clinical manifestations of patients with Langerhans cell histiocytosis (LCH). We explored the presence of BRAFV600E mutation in our cohort of patients ...
Paediatric Langerhans Cell Histiocytosis Disease: Long-Term Sequelae in the Hypothalamic Endocrine System.
(Karger, 2021-11)
Langerhans cell histiocytosis (LCH) is a disorder of the mononuclear phagocyte system that can affect almost any organ and system. The most common central nervous system (CNS) manifestation in LCH is the infiltration of ...
Adult Langerhans cell histiocytosis presenting as metachronous colonic polyps
(Hospital Universitário da Universidade de São PauloSão Paulo, 2013)
Langerhans cell histiocytosis (LCH) is a rare disease characterized by
proliferation of Langerhans-type cells that express CD1a, Langerin (CD207) and
S100 protein. Birbeck granules are a hallmark by ultrastructural ...