Cargando…
Multisystemic Pediatric Langerhans cell histiocytosis: a comprehensive clinico-pathological and BRAF V600E mutation study at autopsy
Langerhans cell histiocytosis (LCH), a disorder of antigen-presenting cells, is the commonest disorder of the mononuclear phagocytic system. Diagnosis is always challenging due to heterogeneous clinical presentation. However, with the evolution and better understanding of its biology, many of these...
Autores principales: | Kapatia, Gargi, Bhatia, Prateek, Singh, Minu, Jain, Richa, Bansal, Deepak, Gupta, Kirti |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hospital Universitário da Universidade de São Paulo
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703466/ https://www.ncbi.nlm.nih.gov/pubmed/33344274 http://dx.doi.org/10.4322/acr.2020.154 |
Ejemplares similares
-
Multicystic encephalomalacia: An autopsy report of 4 cases
por: Madakshira, Manoj Gopal, et al.
Publicado: (2020) -
Lineage switching of the cellular distribution of BRAF(V600E) in multisystem Langerhans cell histiocytosis
por: Milne, Paul, et al.
Publicado: (2022) -
Autopsies
por: Gill, H. D.
Publicado: (1895) -
BRAF V600E-Positive Congenital Multisite Langerhans Cell Histiocytosis
por: Prada Avella, Maria Camila, et al.
Publicado: (2020) -
Multisystem Langerhans Cell Histiocytosis in Adult
por: Garg, Anubhav, et al.
Publicado: (2012)