Results 61 to 70 of about 5,197,064 (280)
A rare case of oral multisystem Langerhans cell histiocytosis [PDF]
, 2017 Langerhans cell histiocytosis (LCH) is a rare disorder characterized by high proliferation of Langerhans dendritic cells. LCH is a solitary or multifocal disease that primarily involves bone tissue and often affects children and young men. A 29 years-old
Facciolo, Maria Teresa +4 more
core +1 more source
Orbital involvement in Rosai-Dorfman disease [PDF]
, 2011 A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni +4 more
core +2 more sources
Pediatric Blood &Cancer, Volume 72, Issue 6, June 2025.ABSTRACT Background Given the limited research on folate and ferritin status in children with cancer undergoing treatment, we investigated the prevalence of abnormalities and their impact on clinical outcomes and treatment complications. Methods This prospective cohort study enrolled children <18 years diagnosed with cancer between August 2010 and ...
Kalum Withey +5 more
wiley +1 more source
LANGERHANS CELLS HISTIOCYTOSIS IN ONE FAMILY [PDF]
Acta Medica Iranica, 2004 Histiocytosis of Langerhans cells (class 1 histiocytosis) consists of a range of clinical manifestations, including bone eosinophilic granuloma, Hand-Schüller-Christian syndrome, and Letterer-Siwe disease. These syndromes represent a spectrum of severity
Sh. Ansari +1 more
doaj +2 more sources
Revista Chilena de RadiologíaIntroducción. La Histiocitosis de células de Langerhans (HCL) es una patología poco frecuente, con diferentes manifestaciones radio-lógicas. Su causa es desconocida y se caracteriza por una proliferación de las células de Langerhans.
Raúl Rojas C +7 more
doaj +1 more source
Griscelli syndrome : a rare neonatal syndrome [PDF]
, 2006 Griscelli syndrome was first described by Griscelli and Siccardi in 1978 in a hospital in Paris. It is a rare autosomal recessive disorder resulting in pigmentary dilution of the skin and hair, presence of large clumps of pigment in hair shafts and an ...
Calvagna, Victor, Ellul, Marthese
core
Sinus Histiocytosis: An Uncommon Presentation of an Uncommon Condition [PDF]
, 2015 Introduction Rosai–Dorfman Disease (RDD), also known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML), is a rare, benign, proliferative disorder of macrophages and monocytes that was first described by Rosai and Dorfman in 1969.
Greco, MD, Allison, Kane, MD, Gregory
core +2 more sources
Pulmonary histiocytosis X. A review of 18 patients with reports of 6 cases.
The American journal of roentgenology, radium therapy, and nuclear medicine, 1969 The chest roentgenograms of 18 patients with pulmonary histiocytosis X were reviewed. Correlation of roentgenographic and histologic changes in 6 patients disclosed a spectrum of changes reflecting the evolutionary character of the pulmonary ...
W. Weber, F. Margolin, S. Nielsen
semanticscholar +1 more source
Adult Langerhans cell histiocytosis with pulmonary and colorectoanal involvement: a case report
Journal of Medical Case Reports, 2017 Background Langerhans cell histiocytosis is a rare systemic disease characterized by the abnormal overproduction of histiocytes that tend to infiltrate single or multiple organ systems leading to significant tissue damage. It mainly affects – by order of
Mohamad Jihad Mansour +4 more
doaj +1 more source
The SUV39 Family of H3K9 Methyltransferases in Skeletal Muscle Stem Cells
FASEB BioAdvances, Volume 7, Issue 6, June 2025.The SUV39 family members are well known for methylating the Lysine 9 of the histone H3 (H3K9) in order to compact the chromatin and contributing to gene repression. We describe their active role in proliferating and differentiating muscle stem cells, how they prevent from inflammation and fibrosis during muscle regeneration and the future avenues ...
Pauline Garcia +2 more
wiley +1 more source