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Year Number of Results
1945 2
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1947 25
1948 36
1949 24
1950 44
1951 60
1952 57
1953 67
1954 85
1955 71
1956 74
1957 77
1958 67
1959 68
1960 63
1961 58
1962 56
1963 104
1964 122
1965 110
1966 82
1967 83
1968 88
1969 122
1970 92
1971 88
1972 80
1973 81
1974 92
1975 93
1976 100
1977 135
1978 111
1979 110
1980 116
1981 134
1982 108
1983 139
1984 153
1985 141
1986 145
1987 131
1988 140
1989 136
1990 167
1991 191
1992 156
1993 208
1994 234
1995 218
1996 204
1997 211
1998 248
1999 239
2000 277
2001 247
2002 262
2003 296
2004 303
2005 240
2006 209
2007 213
2008 254
2009 241
2010 265
2011 264
2012 281
2013 291
2014 345
2015 343
2016 322
2017 344
2018 320
2019 318
2020 357
2021 383
2022 390
2023 336
2024 344
2025 380
2026 22

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13,129 results

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Page 1
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
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.
Langerhans cell histiocytosis is a rare pathology with different clinical manifestations in the neonatal period ranging from isolated bone lesions to systemic compromise. We report a case of Langerhans cell histiocytosis including a liter
Langerhans cell histiocytosis is a rare pathology with different clinical manifestations in the neonatal period ranging
Pulmonary Langerhans Cell Histiocytosis.
Benattia A, Jouenne F, Tazi A. Benattia A, et al. Clin Chest Med. 2025 Dec;46(4):605-618. doi: 10.1016/j.ccm.2025.07.003. Epub 2025 Sep 18. Clin Chest Med. 2025. PMID: 41110924 Review.
Pulmonary Langerhans cell histiocytosis (PLCH) is a rare cystic lung disease that affects young adults with exposure to cigarette smoke. ...The demonstration of constant activation of the mitogen-activated kinase pathway in all Langerhans cell
Pulmonary Langerhans cell histiocytosis (PLCH) is a rare cystic lung disease that affects young adults with exposure to …
Langerhans cell histiocytosis in adults: Advances in pathophysiology and treatment.
Kobayashi M, Tojo A. Kobayashi M, et al. Cancer Sci. 2018 Dec;109(12):3707-3713. doi: 10.1111/cas.13817. Epub 2018 Oct 30. Cancer Sci. 2018. PMID: 30281871 Free PMC article. Review.
Langerhans cell histiocytosis was formerly referred to as histiocytosis X, until it was renamed in 1987. Langerhans cell histiocytosis beta was named for its morphological similarity to skin Langerhans cells. ...
Langerhans cell histiocytosis was formerly referred to as histiocytosis X, until it was renamed in 1987. Lang
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.
More recently, Langerhans cell histiocytosis has been unified into a single concept, though the disease continues to defy traditional classification. By most accounts, Langerhans cell histiocytosis appears to be a morphologically benign p …
More recently, Langerhans cell histiocytosis has been unified into a single concept, though the disease continues to de …
Langerhans cell histiocytosis.
Chu T. Chu T. Australas J Dermatol. 2001 Nov;42(4):237-42. doi: 10.1046/j.1440-0960.2001.00527.x. Australas J Dermatol. 2001. PMID: 11903153 Review.
Langerhans cell histiocytosis is a rare condition that can affect any organ of the body. ...In single system disease, Langerhans cell histiocytosis is responsive to local therapy but, in resistant single system disease or in multisystem d
Langerhans cell histiocytosis is a rare condition that can affect any organ of the body. ...In single system disease,
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 …
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. ...This article reviews our current understanding of Langerhans cell histiocytosis
Langerhans cell histiocytosis (LCH) is a complex disease entity comprised of three distinct clinical syndromes that dem
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
Updates on Langerhans cell histiocytosis and other histiocytosis in children: invited review-challenges and novelties in paediatric tumours.
Galluzzo Mutti L, Picarsic J. Galluzzo Mutti L, et al. Virchows Arch. 2025 Jan;486(1):189-204. doi: 10.1007/s00428-024-04018-w. Epub 2025 Jan 11. Virchows Arch. 2025. PMID: 39794638 Review.
Langerhans cell histiocytosis (LCH), juvenile xanthogranuloma (JXG) family lesions, and Rosai-Dorfman-Destombes disease (RDD) are now classified by the World Health Organization (WHO) under the heading of histiocytic/dendritic cell neoplasms. ...Challe
Langerhans cell histiocytosis (LCH), juvenile xanthogranuloma (JXG) family lesions, and Rosai-Dorfman-Destombes disease
13,129 results
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