Results 11 to 20 of about 324,303 (208)

Imaging features of neonatal systemic juvenile xanthogranuloma: a case report and review of the literature. [PDF]

open access: goldJ Int Med Res, 2020
Juvenile xanthogranuloma (JXG) is the most common non-Langerhans cell histiocytic disorder in children. This report describes the case of a 28-day-old boy that presented with multiple subcutaneous nodular lesions on the trunk and extremities, and ...
He S   +5 more
europepmc   +6 more sources

Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children [PDF]

open access: greenAmerican Journal of Medical Genetics. Part A, 2021
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Lorenzo Calligaris   +6 more
core   +5 more sources

Disseminated Juvenile Xanthogranuloma with a Novel MYH9-FLT3 Fusion Presenting as a Blueberry Muffin Rash in a Neonate. [PDF]

open access: yesAJP Rep, 2023
Juvenile xanthogranuloma (JXG) is a benign proliferative histiocytic disorder of the dendritic cell phenotype. It mostly presents in the pediatric age group as a solitary skin lesion.
Clark EE   +5 more
europepmc   +2 more sources

Solitary juvenile xanthogranuloma of temporal bone: a case report. [PDF]

open access: yesBMC Pediatr, 2022
Background Juvenile xanthogranuloma (JXG) is a kind of non-Langerhans cell histiocytosis, usually with skin lesions as the main manifestation. It rarely occurs in other tissues or organs and even more rarely is it found in the skull.
Wang SN, Lu J.
europepmc   +2 more sources

Juvenile Xanthogranuloma of the Head and Neck: Imaging Findings in 11 Cases. [PDF]

open access: yesJ Pediatr Hematol Oncol
Background: Juvenile Xanthogranuloma (JXG) is a non-Langerhans cell histiocytosis, occurring mainly in infancy. With an extracutaneous lesion, its diagnosis is difficult, because of a wide clinical spectrum.
Chalard F   +8 more
europepmc   +2 more sources

Generalized Eruptive Histiocytosis or Juvenile Xanthogranuloma: A Clinicopathological Conundrum of Coexistence or Xanthomatization. [PDF]

open access: yesIndian Dermatol Online J
Diseases under the non-Langerhans cell histiocytosis (LCH) group often share clinical and histological similarities, making proper delineation highly challenging.
Murthy AB   +3 more
europepmc   +2 more sources

On the knowledge of solitary juvenile xanthogranuloma of the eyelid: a case series and literature review. [PDF]

open access: yesGraefes Arch Clin Exp Ophthalmol, 2022
Solitary eyelid juvenile xanthogranuloma (JXG) is extremely rare, and there is limited literature on its clinical features and treatment outcomes. Here, we present a case series and comprehensive review of the literature on patients with isolated eyelid ...
Chen R   +7 more
europepmc   +2 more sources

Lingual juvenile xanthogranuloma in a woman: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2011
Introduction Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder.
Villa Francesco   +2 more
doaj   +5 more sources

Juvenile Xanthogranuloma as Differential Diagnosis of a Vulvar Mass: A Case Report. [PDF]

open access: yesEuropean J Pediatr Surg Rep, 2022
Vulvar masses in children are an unusual finding but their differential diagnosis is extensive. In case of solid masses, rhabdomyosarcoma (RMS) must always be considered due to the fact that it is the most common tumor in external genitals during ...
Bada Bosch I   +7 more
europepmc   +2 more sources

Juvenile xanthogranuloma in Noonan syndrome. [PDF]

open access: yesAm J Med Genet 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 ...
Ali MM   +4 more
europepmc   +2 more sources

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