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• W3022746245 startingPage "110088" @default.
• W3022746245 abstract "Juvenile Xanthogranuloma (JXG), the most common pediatric non-Langerhans cell histiocytosis, may rarely occur in association with Neurofibromatosis (types 1 and 2), Juvenile Myelomonocytic Leukemia and Cutaneous Mastocytosis (CM) and, morphologically, mimics Erdheim-Chester Disease tissue lesions and ALK-positive histiocytosis. We describe a 4-year-old girl with Beta-Thalassemia Major who developed an hypopharyngeal BRAFV600E- and ALK-negative JXG and CM. JXG has been rarely reported in the aerodigestive tract and in association with CM. In this molecular era, knowledge of genetic heterogeneity of JXG and clinical scenarios in which it may develop is essential for the appropriate diagnosis and treatment of each individual patient." @default.
• W3022746245 created "2020-05-13" @default.
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• W3022746245 date "2020-08-01" @default.
• W3022746245 modified "2023-09-27" @default.
• W3022746245 title "Solitary juvenile xanthogranuloma of the hypopharynx. Clinico-pathologic study in a child with β-Thalassemia Major and Cutaneous Mastocytosis" @default.
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• W3022746245 doi "https://doi.org/10.1016/j.ijporl.2020.110088" @default.
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