Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Adult Langerhans Cell Histiocytosis"'
Autor:
Marcus Y. Chen, Edmond J. FitzGibbon, William A. Gahl, Skand Shekhar, Fady Hannah-Shmouni, Beth Solomon, Rahul Dave, Leora E. Comis, Juvianee Estrada-Veras, Kevin O'Brien, Bernadette R. Gochuico
Publikováno v:
Journal of the National Comprehensive Cancer Network. 19:1312-1318
Adult-onset histiocytoses (AOH), primarily Rosai-Dorfman disease (RDD), Erdheim-Chester Disease (ECD), and adult Langerhans cell histiocytosis (ALCH), are a group of related histiocytic neoplastic disorders featuring multisystemic manifestations. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6309c4d3c9dd3d2a0e7aaa2716b05a1b
https://doi.org/10.6004/jnccn.2021.7096
https://doi.org/10.6004/jnccn.2021.7096
Publikováno v:
NMC Case Report Journal
Langerhans cell histiocytosis (LCH) is a disease characterized by the proliferation of Langerhans cells. Most cases of LCH occur in children, although it can be seen in adults as well. We encountered an adult case of LCH. A 44-year-old woman who was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79608e91ddcf5bfacee84f6823496efc
https://doi.org/10.2176/nmccrj.cr.2020-0094
https://doi.org/10.2176/nmccrj.cr.2020-0094
Autor:
Aishwarya Ravindran, Ronald S. Go, Gordon Ruan, Gaurav Goyal, Robert Vassallo, Jason R. Young, Jithma P. Abeykoon, Caleb Scheckel, W. Oliver Tobin, Karen L. Rech, N. Nora Bennani, Jay H. Ryu, Antonious Z. Hazim, Mithun Vinod Shah, Matthew J. Koster
Publikováno v:
The Oncologist. 25:1001-1004
Langerhans cell histiocytosis (LCH) is a rare histiocytic neoplasm. To date, there is a lack of U.S. Food and Drug Administration–approved treatments in adult LCH to establish optimal first-line therapy. We conducted a retrospective, single-center
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31ff437e77277385ae58b2b4410b120e
https://doi.org/10.1002/onco.13541
https://doi.org/10.1002/onco.13541
Autor:
Minghui Duan, Zhiyong Liang, Jian Sun, Xue-min Gao, Daobin Zhou, Ting Liu, Xinxin Cao, Jian Li, Lu Zhang, Jia Chen, Ai-lin Zhao, Huacong Cai, Hao Cai
Publikováno v:
American journal of hematologyREFERENCES. 97(2)
Adult Langerhans cell histiocytosis (LCH) remains poorly defined. We retrospectively studied 266 newly diagnosed LCH patients to understand the clinical presentation, treatment and prognosis of adult LCH. The median age at diagnosis was 32 years (ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18eb443761be6d98dfa5158fb19d1d62
https://pubmed.ncbi.nlm.nih.gov/34797941
https://pubmed.ncbi.nlm.nih.gov/34797941
Autor:
Christopher Duarte-Celada, Smathorn Thakolwiboon, Walter R. Duarte-Celada, Mirla Avila, Luis Brandi
Publikováno v:
Proc (Bayl Univ Med Cent)
Langerhans cell histiocytosis (LCH), a disorder characterized by aberrant function and proliferation of mononuclear phagocytic cells called Langerhans cells, usually occurs in those
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7668feefd33f58235a4a42613d301c
https://doi.org/10.1080/08998280.2020.1772184
https://doi.org/10.1080/08998280.2020.1772184
Publikováno v:
International Journal of Dermatology and Venerology, Vol 4, Iss 2, Pp 122-124 (2021)
Introduction:. Langerhans cell histiocytosis (LCH), the most common histiocytic disorder, characterized by the abnormal over production of histiocytes that tend to infiltrate single or multiple organ systems leading to significant tissue damage. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fab8a9445a0e2657eacf456f0141fb13
https://doi.org/10.1097/jd9.0000000000000075
https://doi.org/10.1097/jd9.0000000000000075
Publikováno v:
World Journal of Hematology. 8:1-8
Adult Langerhans cell histiocytosis and immunomodulatory drugs: Review and analysis of thirty-four case reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9385933e2b9ac3b8d1cc7e9ed12ee93f
https://doi.org/10.5315/wjh.v8.i1.1
https://doi.org/10.5315/wjh.v8.i1.1
Autor:
In Kyeong Kim, Kyoung Yul Lee
Publikováno v:
BMJ Case Reports
We report an extremely rare case of adult Langerhans cell histiocytosis (LCH) in a patient with papillary thyroid carcinoma (PTC) and Castleman disease (CD). A 46-year-old man visited our hospital with anaemia; systemic imaging showed an abdominal an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19e5e78a81c7b59cb538ba875ab45bab
https://pubmed.ncbi.nlm.nih.gov/33495189
https://pubmed.ncbi.nlm.nih.gov/33495189
Publikováno v:
Journal of Medical Case Reports
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-10 (2020)
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-10 (2020)
Background Langerhans cell tumors are rare clonal disorders characterized by neoplastic proliferation of dendritic cells that can be further classified into the subtypes Langerhans cell histiocytosis and Langerhans cell sarcoma, which are rare neopla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::547cd806f59876a5218c72eb00012515
https://doi.org/10.1186/s13256-020-02460-3
https://doi.org/10.1186/s13256-020-02460-3
Autor:
Jorge Esquiche León, Luciana Yamamoto Almeida, Evânio Vilela Silva, Heitor Albergoni Da Silveira, Fernando Chahud, Glauce L. Trevisan, Léa Assed Bezerra da Silva, Xiomara Beatriz Jimenez Polanco, Silvia Elena Yacarini Paredes, Raquel Assed Bezerra Segato
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Langerhans cell histiocytosis (LCH) is an inflammatory myeloid neoplasia commonly affecting children with frequent somatic mutations in MAPK pathway genes including BRAFV600E and MAP2K1. Some studies suggest that LCH cells can recruit and modulate in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64a12c358008ec6ba51c3da3288cdeb9
https://doi.org/10.1111/sji.12950
https://doi.org/10.1111/sji.12950