Results 91 to 100 of about 56,324 (305)
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
Cancer Medicine, 2018 Langerhans cell histiocytosis (LCH) is a rare disorder of histiocyte proliferation. Previous case studies suggest a higher prevalence of hematologic and solid malignancies among LCH patients, possibly due to treatment with tumorigenic agents such as ...
Jennifer Ma +5 more
semanticscholar +1 more source
Histiocytoid Sweet Syndrome With Paradoxical Neutropenia in a Pediatric Patient
Pediatric Dermatology, EarlyView.ABSTRACT Histiocytoid Sweet syndrome (HSS) is a rare inflammatory skin condition characterized by the infiltration of mononuclear cells in the dermis and leukocytosis with neutrophilia. This uncommon variant of classic Sweet syndrome is rarely reported in the literature, especially in pediatric patients.
Shelby Boock +3 more
wiley +1 more source
18F-FDG PET/MR Assessment of Pediatric Langerhans Cell Histiocytosis
International Journal of General Medicine, 2021 Jialing Niu,1,2 Jiangtao Liang,3 Qi Feng,2 Mei Wang,2 Luoyu Wang,4 Xiuhong Ge,2 Xiao Wang,5 Zhongxiang Ding2,6 1Zhejiang Chinese Medical University, Hangzhou, People’s Republic of China; 2Department of Radiology, Affiliated Hangzhou First People’s ...
Niu J +7 more
doaj
Differentiation of intracranial Rosai‐Dorfman histiocytosis from meningioma using MR perfusion
Clinical Case Reports, 2022 Intracranial Rosai‐Dorfman disease may be indistinguishable from meningioma. This distinction is essential, as they are treated very differently. We present two cases where perfusion imaging helped make this distinction, allowing one to be treated ...
Hugo F. Bueno +5 more
doaj +1 more source
Single-agent dabrafenib for BRAFV600E-mutated histiocytosis
Haematologica, 2018 Langerhans cell histiocytosis (LCH) and Erdheim-Chester disease (ECD) are clonal disorders of the monocyte/macrophage and dendritic cell lineages characterized by infiltration of histiocytes, acute and chronic inflammation, and fibrosis that can involve ...
A. Bhatia +11 more
semanticscholar +1 more source
Paediatric and Perinatal Epidemiology, EarlyView.Abstract Background Cancer is the leading cause of death in children aged 1–14 and the second in 15‐19‐year‐old adolescents in Spain. The Paediatric Population‐Based Cancer Registry of the Community of Madrid was created to monitor its incidence and survival.
Raquel López‐González +5 more
wiley +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
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
Multicentric reticulohistiocytosis: A rare case report
Indian Journal of Dermatology, 2012 A 58-year-old lady presented with polyarthritis followed by multiple shiny erythematous dome-shaped papulonodules mainly over the face, around joints and coral bead sign on fingers without any mucosal involvement.
Soumya Mukherjee +1 more
doaj +1 more source