Results 91 to 100 of about 55,121 (305)
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
Emergence of solitary juvenile xanthogranuloma on the corneoscleral limbus
Journal of Clinical Ophthalmology and Research, 2018 Juvenile xanthogranuloma (JXG) is the most frequent form of non-Langerhans histiocytosis, a rare benign inflammatory skin disorder. Eye involvement is the most frequent extracutaneous manifestation of the disease.
Raul Alfaro-Rangel +2 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
Effective BRAF inhibitor vemurafenib therapy in a 2-year-old patient with sequentially diagnosed Langerhans cell histocytosis and Erdheim-Chester disease [PDF]
, 2017 Erdheim–Chester disease (ECD) is a rare histiocytic disorder, characterized by the xanthomatous infiltration of tissues by CD68-positive and CD1a-/CD100-negative foamy histiocytes. In childhood, ECD is exceptionally rare, and only a dozen cases have been
Bánusz, Rita +6 more
core +2 more sources
Atypical Presentation of IARS1‐Related Disorder: Expanding the Phenotype and Genotype
JIMD Reports, Volume 66, Issue 3, May 2025.ABSTRACT Aminoacyl‐tRNA synthetases (ARSs) catalyze the formation of aminoacyl‐tRNA, which is required for protein translation. A growing number of cases are associated with ARS deficiencies. Pathogenic variants in IARS1 (MIM# 600709), encoding cytoplasmic isoleucyl‐tRNA synthetase, have been associated with autosomal recessive growth retardation ...
Parith Wongkittichote +7 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
Growth of children with Langerhans cell histiocytosis [PDF]
, 1995 Conclusion: GH deficiency is not a common manifestation of LCH in childhood and GH provocation tests are only indicated when there is a poor or decelerating growth rate.
Egeler, R.M. (Maarten) +3 more
core +1 more source
How I treat Langerhans cell histiocytosis.
Blood, 2015 "Langerhans cell histiocytosis" (LCH) describes a spectrum of clinical presentations ranging from a single bone lesion or trivial skin rash to an explosive disseminated disease.
C. Allen, S. Ladisch, K. McClain
semanticscholar +1 more source
Familial polyposis syndrome and achalasia in a young adult
JPGN Reports, Volume 6, Issue 2, Page 166-169, May 2025.Abstract We report the case of a 19‐year‐old White male diagnosed with familial adenomatous polyposis (FAP), Gardner's syndrome (GS) phenotype, status post total colectomy, who developed progressive dysphagia and weight loss. He was diagnosed with achalasia based on imaging and esophageal manometry.
Gabriella A. Lorusso Vivas +2 more
wiley +1 more source
Oral manifestation of Langerhans cell histiocytosis: a case report
BMC Oral Health, 2018 Bone necrosis of the jaw is a serious condition with a broad differential diagnosis of pathologies such as cutaneous histiocytosis, bone metastases or malignant tumours.
J. Luz +5 more
semanticscholar +1 more source