Results 191 to 200 of about 317,416 (245)
Some of the next articles are maybe not open access.
Pediatric Neurosurgery, 2021
Introduction: Juvenile xanthogranuloma (JXG) is a disorder of histiocytic proliferation that affects young children and usually presents as spontaneously regressing cutaneous lesions.
Emre Bilgin, A. I. Ökten
semanticscholar +1 more source
Introduction: Juvenile xanthogranuloma (JXG) is a disorder of histiocytic proliferation that affects young children and usually presents as spontaneously regressing cutaneous lesions.
Emre Bilgin, A. I. Ökten
semanticscholar +1 more source
Ocular Juvenile Xanthogranuloma
Optometry and Vision Science, 2015To report the clinical and histopathologic characteristics and prognoses of three ocular juvenile xanthogranuloma (JXG) cases.Three cases were included in this study. The first case involved a 5-year-old girl with an enlarging yellowish mass at the limbus with corneal involvement.
Fanrong Meng+6 more
openaire +3 more sources
Ocular Juvenile Xanthogranuloma With BRAF V600E Mutation in a Child.
Journal of pediatric ophthalmology and strabismus, 2021The authors present a case of bilateral painless progressive proptosis. A diagnosis of ocular juvenile xanthogranuloma was made based on clinical manifestations, histopathology, and immunohistochemistrical staining.
Chengyue Zhang+3 more
semanticscholar +1 more source
Juvenile Xanthogranuloma and Neurofibromatosis
Archives of Dermatology, 1973The finding of neurofibromatosis in patients or in relatives of patients with juvenile xanthogranuloma is intriguing. To our knowledge, this association has not been emphasized in the American dermatologic literature.
Gordon B. Newell+2 more
openaire +3 more sources
Treatment of juvenile xanthogranuloma [PDF]
AbstractJuvenile xanthogranuloma (JXG) is generally a benign, self‐limited histiocytic disorder of the skin. We report two cases of multisystem JXG presenting with clinical features more commonly seen in Langerhans cell histiocytosis (LCH), including diabetes insipidus and lytic bony lesions.
Daniel G. Stover+4 more
openaire +2 more sources
Juvenile Xanthogranuloma of the Testis
Journal of Urology, 1985A 7-month-old boy presented with numerous xanthomatous skin lesions and a hard irregular swelling of the right testis. Clinically, the testicular lesion was impossible to distinguish from a malignant neoplasm. Histological examination of a skin biopsy and of the testis following orchiectomy showed lesions typical of juvenile xanthogranuloma.
A. Gledhill+3 more
openaire +3 more sources
Juvenile xanthogranuloma of the tongue
Journal of the American Academy of Dermatology, 1995Oral juvenile xanthogranuloma is a rare condition, with only 10 histologically proven cases previously described. A histologically unusual variant is reported here, diagnosis of which was aided by the use of immunohistochemical stains. Previously reported cases are reviewed, and their characteristics are tabulated and discussed.
Sarah J Satow+5 more
openaire +3 more sources
Pediatric Orbital Juvenile Xanthogranuloma: A Case Series and Review of the Literature
Ophthalmic Plastic and Reconstructive SurgeryPurpose: Juvenile xanthogranuloma (JXG) is a subtype of histiocytosis characterised histologically by foamy non-Langerhan cells with Touton giant cells.
Ming-Han H Lee+4 more
semanticscholar +1 more source
Journal of pediatric hematology/oncology, 2021
Juvenile xanthogranuloma (JXG) is a rare, non–Langerhans cell histiocytosis. It is usually a benign and self-limiting condition. The most common sites are skin and soft tissue. Pancreatic involvement is extremely rare.
Eman Al-Antary+4 more
semanticscholar +1 more source
Juvenile xanthogranuloma (JXG) is a rare, non–Langerhans cell histiocytosis. It is usually a benign and self-limiting condition. The most common sites are skin and soft tissue. Pancreatic involvement is extremely rare.
Eman Al-Antary+4 more
semanticscholar +1 more source
Glaucoma in Juvenile Xanthogranuloma
Seminars in Ophthalmology, 2006Juvenile xanthogranuloma (JXG) is a benign histiocytic skin disorder mainly encountered during infancy. Approximately 10% of cases exhibit ocular manifestations leading to serious complications. Specifically, secondary glaucoma can result in severe and blinding eye disease.
Zarmeena Vendal+2 more
openaire +3 more sources