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Langerhans-Cell Histiocytosis.
Allen CE, Merad M, McClain KL. Allen CE, et al. N Engl J Med. 2018 Aug 30;379(9):856-868. doi: 10.1056/NEJMra1607548. N Engl J Med. 2018. PMID: 30157397 Free PMC article. Review. No abstract available.
Langerhans cell histiocytosis in children: History, classification, pathobiology, clinical manifestations, and prognosis.
Krooks J, Minkov M, Weatherall AG. Krooks J, et al. J Am Acad Dermatol. 2018 Jun;78(6):1035-1044. doi: 10.1016/j.jaad.2017.05.059. J Am Acad Dermatol. 2018. PMID: 29754885 Review.
Langerhans cell histiocytosis (LCH) is an inflammatory neoplasia of myeloid precursor cells driven by mutations in the mitogen-activated protein kinase pathway. ...
Langerhans cell histiocytosis (LCH) is an inflammatory neoplasia of myeloid precursor cells driven by mutations in the …
Pulmonary Langerhans' cell histiocytosis in adults.
Radzikowska E. Radzikowska E. Adv Respir Med. 2017;85(5):277-289. doi: 10.5603/ARM.a2017.0046. Epub 2017 Oct 30. Adv Respir Med. 2017. PMID: 29083024 Free article. Review.
Pulmonary Langerhans' cell histiocytosis (PLCH) is a rare disorder of unknown cause characterised by the infiltration of the lungs and other organs by the bone marrow derived Langerhans' cells, which carry mutations of BRAF gene and/or NRAS, KRAS and M …
Pulmonary Langerhans' cell histiocytosis (PLCH) is a rare disorder of unknown cause characterised by the infiltration o …
Congenital Langerhans cell histiocytosis.
Barrios K, Patiño O, Muñoz N, Moneriz C. Barrios K, et al. Biomedica. 2020 Sep 1;40(3):464-471. doi: 10.7705/biomedica.5150. Biomedica. 2020. PMID: 33030824 Free PMC article. Review. English, Spanish.
We report a case of Langerhans cell histiocytosis including a literature review focused on the clinical manifestations, diagnosis, and treatment. ...We report a case of Langerhans cell histiocytosis including a literature review focused o …
We report a case of Langerhans cell histiocytosis including a literature review focused on the clinical manifestations, …
Langerhans cell histiocytosis.
Margo CE, Goldman DR. Margo CE, et al. Surv Ophthalmol. 2008 Jul-Aug;53(4):332-58. doi: 10.1016/j.survophthal.2008.04.007. Surv Ophthalmol. 2008. PMID: 18572052 Review.
The clinical manifestations of Langerhans cell histiocytosis have been recognized for more than a century. ...By most accounts, Langerhans cell histiocytosis appears to be a morphologically benign proliferation of inflammatory cells that …
The clinical manifestations of Langerhans cell histiocytosis have been recognized for more than a century. ...By most a …
Langerhans cell histiocytosis.
Hoover KB, Rosenthal DI, Mankin H. Hoover KB, et al. Skeletal Radiol. 2007 Feb;36(2):95-104. doi: 10.1007/s00256-006-0193-2. Epub 2006 Oct 7. Skeletal Radiol. 2007. PMID: 17028900 Review.
Langerhans cell histiocytosis (LCH) is a complex disease entity comprised of three distinct clinical syndromes that demonstrate indistinguishable histology. These syndromes are: eosinophilic granuloma, which is predominantly osseous or pulmonary; Hand-Schulle …
Langerhans cell histiocytosis (LCH) is a complex disease entity comprised of three distinct clinical syndromes that dem …
Langerhans cell histiocytosis (LCH): guidelines for diagnosis, clinical work-up, and treatment for patients till the age of 18 years.
Haupt R, Minkov M, Astigarraga I, Schäfer E, Nanduri V, Jubran R, Egeler RM, Janka G, Micic D, Rodriguez-Galindo C, Van Gool S, Visser J, Weitzman S, Donadieu J; Euro Histio Network. Haupt R, et al. Pediatr Blood Cancer. 2013 Feb;60(2):175-84. doi: 10.1002/pbc.24367. Epub 2012 Oct 25. Pediatr Blood Cancer. 2013. PMID: 23109216 Free PMC article.
These guidelines for the management of patients up to 18 years with Langerhans cell histiocytosis (LCH) have been set up by a group of experts involved in the Euro Histio Net project who participated in national or international studies and in peer reviewed p …
These guidelines for the management of patients up to 18 years with Langerhans cell histiocytosis (LCH) have been set u …
Pulmonary Langerhans-Cell Histiocytosis.
Qanneta R, Raventos-Estelle A. Qanneta R, et al. N Engl J Med. 2022 Dec 29;387(26):2449. doi: 10.1056/NEJMicm2203885. Epub 2022 Dec 24. N Engl J Med. 2022. PMID: 36573701 No abstract available.
Langerhans cell histiocytosis.
Windebank K, Nanduri V. Windebank K, et al. Arch Dis Child. 2009 Nov;94(11):904-8. doi: 10.1136/adc.2007.125872. Epub 2009 May 19. Arch Dis Child. 2009. PMID: 19457881 Review.
Langerhans cell histiocytosis is a rare disease. Depending on which organs are involved, the disease may prove rapidly fatal, develop a chronic reactivating but therapy-responsive pattern or resolve spontaneously. ...
Langerhans cell histiocytosis is a rare disease. Depending on which organs are involved, the disease may prove rapidly …
Langerhans cell histiocytosis.
Herzog KM, Tubbs RR. Herzog KM, et al. Adv Anat Pathol. 1998 Nov;5(6):347-58. doi: 10.1097/00125480-199811000-00001. Adv Anat Pathol. 1998. PMID: 10095876 Review.
Langerhans cell histiocytosis (LCH) is a rare clonal disorder that consists of single or multiple mass lesions composed of cells with an abnormal Langerhans cell phenotype. ...Similarly, the pathogenesis of the disease is enigmatic, although the …
Langerhans cell histiocytosis (LCH) is a rare clonal disorder that consists of single or multiple mass lesions composed …
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