Zobrazeno 1 - 10
of 426
pro vyhledávání: '"LETTERER-Siwe disease"'
Autor:
H. H., Suad1 Dr.suadhassan4@gmail.com, Elamin, Mona Mohamed2, Modawe, Gad Allah3, Awad Elseed, Khalid Abd Elmohsin4
Publikováno v:
Sudan Journal of Medical Sciences. Sep2018, Vol. 13 Issue 3, p207-218. 12p.
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 23, Iss 2, Pp 129-132 (2022)
Langerhans cell histiocytosis is a rare clonal disease of monocyte-macrophage system characterized with uncontrolled proliferation and accumulation of immature dendritic cells. Acute disseminated form of this disease known as Letterer-Siwe disease is
Externí odkaz:
https://doaj.org/article/d4e154883eca49828d10219c7a4a11f0
Publikováno v:
Sudan Journal of Medical Sciences, Vol 13, Pp 1-12 (2018)
Background: Letterer–Siwe Disease (LSD) is one of the variants of Langerhans cell histiocytosis (LCH), which is considered as a rare disease that affects many systems in the body; it is characterized by monoclonal migration and proliferation of spe
Externí odkaz:
https://doaj.org/article/31e1277986ca403c96fdcbb594888eee
Autor:
Alanazi, Latifa1 Latifafahad.a@gmail.com, Alhindi, Ghada1, Alanazi, Yara1, Alseneidi, Sarah1, Alanazi, Bashayer2, Alshagha, Dalal1, Alghufaily, Munira1
Publikováno v:
International Archives of Integrated Medicine. 2018, Vol. 5 Issue 9, p133-142. 10p.
Autor:
Subbarao
Publikováno v:
Journal of Medical and Scientific Research, Vol 5, Iss 1, Pp 33-39 (2017)
Langerhans histiocytosis is the recent term used for the complex syndrome consisting of three sub types 1. Eosinophilic granuloma, 2. Hand-Schuller Christian disease and 3. Letterer-siwe disease. The clinical manifestations vary with each entity. Alt
Externí odkaz:
https://doaj.org/article/4aa86d483e5049ddb30471d56d4f0fa3
Akademický článek
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Publikováno v:
Acta Paediatrica. Mar2004, Vol. 93 Issue 3, p426-429. 4p.
Publikováno v:
Indian Journal of Pathology and Oncology. 8:508-511
Background: Histiocytes with coffee bean like nucleus are the diagnostic hallmark of Langerhans cell histiocytosis (LCH) supported with immunohistochemical (IHC) demonstration of fascin, CD1a and S-100. We report a case of Letterer-Siwe disease in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62e4d309268028e862245e1e1139d025
https://doi.org/10.18231/j.ijpo.2021.105
https://doi.org/10.18231/j.ijpo.2021.105
Publikováno v:
Journal of Oral Pathology. Dec81, Vol. 10 Issue 6, p386-397. 12p.
Autor:
Glass, Andrew G., Miller, Robert W.
Publikováno v:
Pediatrics. Aug68, Vol. 42 Issue 2, p364. 4p.