Results 51 to 60 of about 319,608 (239)
Case Reports in Dermatology, 2021 Juvenile xanthogranuloma (JXG) is the most common type of non-Langerhans cell histiocytosis. JXG is a rare benign tumor, which may be present at birth or develop later. The classical form of JXG is characterized by a red-yellowish benign papule or nodule
Kaspar Itin +3 more
semanticscholar +1 more source
Bilateral Spontaneous Hyphaema in Juvenile Xanthogranuloma: A case report and literature review [PDF]
, 2008 Background: A four-month-old Nigerian male was presented with spontaneous hyphaema in both eyes initially thought to be due to trauma or possibly non accidental injury.
Adio, AO, Fieba, B, Nathaniel, GI
core +2 more sources
Exceptionally large juvenile xanthogranuloma – a case report [PDF]
, 2023 Juvenile xanthogranuloma (JXG) is a rare, benign skin lesion pathologically classified as a non-Langerhans cell histiocytosis. The lesions appear within the first year of life in 75% of patients, predominantly on the head or neck, growing up to 5mm in ...
Brenner, Eva +2 more
core +2 more sources
Juvenile xanthogranuloma of the cerebellopontine angle: A case report and review of the literature
Otolaryngology Case Reports, 2019 Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis, most often presenting with skin lesions of the head, neck, and upper trunk. Intracranial presentations have been previously described, however, due to its rarity, treatment algorithms
Sarah M. Tittman +6 more
doaj +1 more source
Juvenile xanthogranuloma in Noonan syndrome
American Journal of Medical Genetics. Part A, 2021 Noonan syndrome (NS) is one of the common RASopathies. While the clinical phenotype in NS is variable, it is typically characterized by distinctive craniofacial features, cardiac defects, reduced growth, bleeding disorders, learning issues, and an ...
Marwan M Ali +4 more
semanticscholar +1 more source
Cutaneous findings in neurofibromatosis type 1 [PDF]
, 2021 Neurofibromatosis type 1 (NF1) is characterized by major and minor cutaneous findings, whose recognition plays a key role in the early diagnosis of the disease.
Argenziano G. +4 more
core +1 more source
Congenital Juvenile Xanthogranuloma of Foot, a Nodular Lesion: An Unusual Case in 2-month-old Infant [PDF]
, 2021 A 2-month-old infant presented with a circumscribed nodule on left foot since birth. Excision biopsy showed juvenile xanthogranuloma, an uncommon diagnosis in an unusual site; common sites being head and neck.
Anand K Verma +4 more
core +1 more source
Neoadjuvant intralesional methotrexate for juvenile xanthogranuloma in an adult [PDF]
, 2021 Juvenile xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis usually occurring in infants and typically located in the head or neck.1 Clinically, solitary skin lesions are found in 60%–82% of patients and the most common variant is characterized
Antoñanzas, J. (Javier) +6 more
core +1 more source
Neonatal Systemic Juvenile Xanthogranuloma with an Ominous Presentation and Successful Treatment [PDF]
, 2011 This case report originated from a case of neonatal multisystemic juvenile xanthogranuloma (JXG). The patient presented with blue muffin rush, cervical mass, bone destruction, lung nodule, hepatosplenomegaly, and coagulopathy and was successfully treated
Fan, Rong, Sun, Jihong
core +2 more sources
Solitary Xanthogranuloma of the Upper Cervical Spine in a Male Adult [PDF]
, 2012 We present the rare case of solitary xanthogranuloma in the upper cervical column mimicking a Brown-Sequard syndrome. A 29-year-old man complained with right hemiparesis and left hypoesthesia after a car accident.
Jo, Dae Jean +3 more
core +2 more sources