Results 111 to 120 of about 55,121 (305)
مجله دانشکده پزشکی اصفهان, 2010 Background: Patients with Langerhans cell histiocytosis are at particularly high risk for central diabetes insipi-dus (CDI) due to hypothalamic-pituitary disease. Langerhans cell histiocytosis (LCH) is a group of idiopathic disorders characterized by the
Zahra Alian +2 more
doaj
Bagaimana Prognosis Histiocytosis? Sebuah Laporan Kasus [PDF]
, 2013 Penderita histiocytosis dengan keterlibatan multiorgan dan disertai gangguan fungsi organ mempunyai prognosis buruk dan tingkat mortalitas tinggi. Dilaporkan seorang penderita histiocytosis, usia 1 tahun 1 bulan yang datang dengan kelainan di kulit ...
Lestari, R. D. (Rini) +1 more
core
Langerhans cell histiocytosis in adults: a case report and review of the literature
OncoTarget, 2016 Background Langerhans cell histiocytosis (LCH) is a proliferative disease of histiocyte-like cells that generally affects children. Immunohistochemistry is essential to obtain the correct diagnosis, and treatment protocols are controversial.
Cui Lian, Yuan Lu, Siyuan Shen
semanticscholar +1 more source
Langerhans Cell Histiocytosis as Cause of Central Diabetes Insipidus: Case Report
Brazilian Neurosurgery, 2018 Langerhans cell histiocytosis (LCH) is a rare disease of the monocyte-macrophage system, characterized by the aberrant proliferation of specific dendritic cells.
Diana Quirino Nascimento +2 more
doaj +1 more source
Recurrent BRAF mutations in Langerhans cell histiocytosis.
Blood, 2010 Langerhans cell histiocytosis (LCH) has a broad spectrum of clinical behaviors; some cases are self-limited, whereas others involve multiple organs and cause significant mortality.
G. Badalian‐Very +14 more
semanticscholar +1 more source
Soft Tissue Rosai-Dorfman Disease: Case report
Sultan Qaboos University Medical Journal, 2018 Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by massive lymphadenopathy. While extranodal involvement can occur in generalised RDD, isolated soft tissue RDD (STRDD) is extremely rare.
Rubyath C. Rajib +3 more
doaj +1 more source
Dendritic Cells Cause Bone Lesions in a New Mouse Model of Histiocytosis. [PDF]
, 2015 Langerhans cell histiocytosis (LCH) is a rare disease caused by the clonal accumulation of dendritic Langerhans cells, which is often accompanied by osteolytic lesions.
Acha-Orbea, H. +11 more
core +3 more sources
Proceedings of the Royal Society of Medicine, 1969 S, Bor, I, Smith, M, Feiwel
openaire +2 more sources
Langerhans' Cell Histiocytosis
Dermatology Online Journal, 2002 Adult onset Langerhans cell histiocytosis is uncommon. A 29 year old man is presented who developed classic cutaneous disease with severe systemic involvement. He responded completely to a two month course of thalidomide.
Mortazavi, Hessein +3 more
openaire +4 more sources